Patent Application
20210147795
The present application claims priority under 35 U.S.C. § 119 to Japanese Patent Application No. 2019-207225, filed on Nov. 15, 2019. The contents of which are incorporated herein by reference in their entirety.
The present invention relates to a layered body used in cell culture techniques in vitro.
Examples of in vitro cell culture techniques include a technique called co-culture, in which a plurality of types of cells are cultured in the same container. One common method of co-culture is a contact method in which a plurality of types of cells are cultured simultaneously on the same plane, and another is a non-contact method in which a plurality of types of cells are cultured, for example, separated up and down, through a membrane called an insert, through which cells are not allowed to pass through. The contact method can evaluate effects of direct contact between cells of different types and paracrine effects of proteins secreted by cells into a medium on other cells, while the non-contact method can evaluate paracrine effects by proteins secreted by cells in an insert.
In the contact method, each cell cannot be recognized when detecting the paracrine effect, and it is necessary to use a separate marker to distinguish cells in order to examine the paracrine effect on each cell. On the other hand, in the non-contact method, an effect on each cell is distinguishable because cells are separated by an insert, but a detected paracrine effect is diluted and weakened because proteins (signal factors) secreted by the cells diffuse into a medium, which is problematic.
As a conventional technique for arranging a plurality of types of cells in a non-contact state, (Non-Patent Document 1) discloses a configuration in which one type of multi-layered cell layer is arranged in an insert and a spheroid in which cells of another type are made spherical with hydrogel on the back side of the insert for the purpose of forming a mucus layer by co-culture. Patent Document 1 discloses a configuration in which cells are made into sheets and gelatin hydrogel particles are sandwiched between the cell sheets to form a three-layered cell sheet for the purpose of maintaining cell survival.
However, it is difficult to detect the paracrine effect on each cell with the above-described conventional techniques with high intensity.
[Patent Document 1] WO2014/192909
[Non-Patent Document 1] Quaozhi Lu, et al., “An In Vitro Model for the Ocular Surface and Tear Film System,” SCIENTIFIC REPORTS, 7:6163
Accordingly, an object of the present invention is to provide a layered body of cells that is used in a co-culture technique and that is capable of recognizing a paracrine effect of each cell and detecting the effect with high intensity.
In order to solve the above-described problem, the layered body of the present invention is a layered body having a layered structure in which a gel layer containing a hydrogel is disposed between at least two cell layers containing cells of different types from each other, wherein the hydrogel is a multi-branched polymer hydrogel formed by a reaction of: Liquid A containing a multi-branched polymer A, the polymer containing, as a backbone, a polyethylene glycol containing at least three branches, the branches containing one or more electrophilic functional groups in at least one of a side chain(s) and an end(s); and Liquid B containing a multi-branched polymer B, the polymer containing, as a backbone, a polyethylene glycol containing at least three branches, the branches containing one or more nucleophilic functional groups in at least one of a side chain(s) and an end(s), the concentration of components derived from the multi-branched polymers A and B in the hydrogel is from 0.6% by weight to 8% by weight, and the thickness is from 0.02 mm to 2 mm.
The layered body of the present invention can be used for co-culture of a plurality of types of cells, in which a paracrine effect for each cell can be recognized. A layered body by which such a paracrine effect is exhibited with high intensity can be provided.
The present invention is described below in detail according to embodiments.
Since the embodiments described below are preferred embodiments of the present invention, various technically preferred limitations are given to the embodiments. However, as long as there is no description indicating limitation of the present invention in the following description, the scope of the present invention is not limited to these modes.
A first embodiment of the present invention will be described based on
The type and the like of the cells contained in the cell layers 10a and 10b are not limited, and may be appropriately selected depending on the purpose. In terms of taxonomy, the cells may be, for example, eukaryotic cells, prokaryotic cells, multicellular organism cells, unicellular organism cells, or the like. Any cells may be used. The cells are preferably adhesive cells having cell adhesiveness which is enough to allow adhesion of the cells to each other and to prevent isolation of the cells from each other as long as the cells are not subjected to a physicochemical treatment.
The adherent cells are not limited, and may be appropriately selected depending on the purpose. Examples of the adhesive cells include differentiated cells and undifferentiated cells.
Examples of the differentiated cells include hepatocytes as parenchymal cells of the liver; stellate cells; Kupffer cells; vascular endothelial cells; endothelial cells such as sinusoidal endothelial cells and corneal endothelial cells; fibroblasts; osteoblasts; osteoclasts; periodontal membrane-derived cells; epidermal cells such as epidermal keratinocytes; tracheal epithelial cells; gastrointestinal epithelial cervical epithelial epithelial cells, such as corneal epithelial cells; mammary cells; pericytes; muscle cells such as smooth muscle cells and cardiomyocytes; kidney cells; pancreatic Langerhans islet cells; nerve cells such as peripheral nerve cells and optic nerve cells; chondrocytes; and bone cells. The adhesive cells may be primary cells directly collected from a tissue or an organ, or may be subcultured cells obtained after several passages.
The undifferentiated cells are not limited, and may be appropriately selected depending on the purpose. Examples of the undifferentiated cells include pluripotent stem cells, such as embryonic stem cells, which are undifferentiated cells, and mesenchymal stem cells, which have pluripotency; unipotent stem cells such as vascular endothelial progenitor cells, which have unipotency; and iPS cells.
The density of cells in the cell layers 10a and 10b is not limited, and the cells may be directly bound to each other. The cells are preferably seeded at a seeding density of, for example, 5,000 to 60,000 cells/cm2.
The cell layers 10a and 10b may contain materials such as various extracellular substrates or media as needed, which may be filled between the cells. The extracellular substrate is not limited, and may be appropriately selected depending on the purpose. For example, extracellular substrate proteins such as collagen, laminin, fibronectin, elastin, fibrin, proteoglycans, hyaluronic acid, heparan sulfate proteoglycans, or chondroitin sulfate proteoglycans, glycoproteins, and proliferation/growth factors such as hepatocyte growth factor, fibroblast growth factor, or nerve growth factor depending on the cell may be used. Any one type of these cells may be used individually, or two or more types of these cells may be used in combination. These are known to promote cell adhesion, proliferation, and differentiation, and can trigger changes in cell morphology when these cells are contained in the cell layer.
The culture medium is a solution containing components required for formation and maintenance of the three-dimensional structure. The medium prevents drying, and controls the external environment including the osmotic pressure. The culture medium is not limited, and may be appropriately selected from known culture media depending on the intended use. For a three-dimensional structure which does not need to be constantly immersed in a culture medium, such as skin whose surface is exposed to air, the culture medium may be removed as appropriate.
The culture medium is not limited, and may be appropriately selected depending on the purpose. Examples of the culture medium include various culture media classified according to the composition, such as natural media, semi-synthetic media, and synthetic media; and various culture media classified according to the shape, such as semi-solid media, liquid media, and powder media. Any one of these culture media may be used individually, or two or more types of these culture media may be used in combination. In cases where the cells are derived from an animal, any culture medium for use in animal cell culture may be used.
The culture medium for use in animal cell culture is not limited, and may be appropriately selected depending on the purpose. Examples of the culture medium include Dulbecco's Modified Eagle's Medium (D-MEM), Ham's F12 medium (Ham's Nutrient Mixture F12), D-MEM/F12 medium, McCoy's 5A medium, Eagle's MEM medium (Eagle's Minimum Essential Medium (EMEM)), αMEM medium (alpha Modified Eagle's Minimum Essential Medium; αMEM), MEM medium (Minimum Essential Medium), RPMI 1640 medium, Iscove's Modified Dulbecco's Medium (IMDM), MCDB131 medium, William's medium E, IPL 41 medium, Fischer's medium, StemPro 34 (manufactured by Invitrogen), X-VIVO 10 (manufactured by Cambrex Corporation), X-VIVO 15 (manufactured by Cambrex Corporation), HPGM (manufactured by Cambrex Corporation), StemSpan H3000 (manufactured by StemCell Technologies Inc.), StemSpan SFEM (manufactured by StemCell Technologies Inc.), Stemline II (manufactured by Sigma-Aldrich), QBSF-60 (manufactured by Quality Biological, Inc.), StemPro hESC SFM (manufactured by Invitrogen), Essential 8 (registered trademark) medium (manufactured by Gibro), mTeSR-1 or −2. medium (manufactured by StemCell Technologies Inc.), Repro FF or Repro FF2 (manufactured by ReproCELL Inc.), PSGro hESC/iPSC medium (manufactured by System Biosciences, Inc.), NutriStem (registered trademark) medium (manufactured by Biological Industries), CSTI-7 medium (manufactured by Cell Science & Technology Institute, Inc.) MesenPRO RS medium (manufactured by Gibco), MF-Medium (registered trademark) mesenchymal stem cell growth medium (manufactured by Toyobo Co., Ltd.). Sf-900II (manufactured by Invitrogen), and Opti-Pro (manufactured by Invitrogen). Any one type of these culture media may be used individually, or two or more of these culture media may be used in combination.
The carbon dioxide concentration in the culture medium is not limited, and may be appropriately selected depending on the purpose. The carbon dioxide concentration is preferably from 2% to 5%, more preferably from 3% to 4%. In cases where the carbon dioxide concentration is from 2% to 5%, the cells can be appropriately cultured.
The hydrogel contained in the gel layer 20a is a multi-branched polymer hydrogel formed by a reaction of: Liquid A containing a multi-branched polymer A, the polymer containing, as a backbone, a polyethylene glycol containing at least three branches, the branches containing one or more electrophilic functional groups in at least one of a side chain(s) and an end(s); and Liquid B containing a multi-branched polymer B, the polymer containing, as a backbone, a polyethylene glycol containing at least three branches, the branches containing one or more nucleophilic functional groups in at least one of a side chain(s) and an end(s). Each component is described below.
The multi-branched polymer containing a polyethylene glycol as a backbone is a polymer containing three or more polyethylene glycol branches, wherein molecules of the polymer cross-link to each other to form a network structure. In particular, four-branched polymers form homogeneous network structures, and gels having a four-branched polyethylene glycol backbone are generally known as Tetra-PEG gels. A Tetra-PEG has a network structure formed by cross-end coupling reaction between two kinds of four-branched polymers each containing an electrophilic functional group or a nucleophilic functional group in at least one of a side chain(s) and an end(s).
A past study has reported that a Tetra-PEG gel has an ideal homogeneous network structure (Matsunaga T. et al., Macromolecules, Vol. 42, No. 4, pp. 1344-1351 (2009)). A Tetra-PEG gel can be simply prepared on site by mixing of two polymer liquids, and the gelation time can be controlled by adjusting the pH and the polymer concentration of each polymer liquid (which corresponds to each of Liquid A and Liquid B in the present invention). By allowing the Liquid A and the Liquid B to react, and then allowing gelation of the liquids to form a Tetra-PEG gel, a gel layer 20a can be produced. Since the gel layer 20a contains a polyethylene glycol as a major component, the gel layer has excellent biocompatibility, and a paracrine effect in which proteins secreted from a cell layer 10a act on another cell layer 10b (or vice versa) can be evaluated at a high concentration.
The total number of the electrophilic functional group(s) in the polymer in Liquid A and the nucleophilic functional group(s) in the polymer in Liquid B is preferably not less than 6. Although these functional groups may be present in one or both of a side chain(s) and an end(s) of each polymer, the functional groups are preferably present in an end(s) of each polymer. The content of the electrophilic functional group in the polymer in Liquid A may be higher than the content of the nucleophilic functional group in the polymer in Liquid B in the composition. Alternatively, the content of the nucleophilic functional group in the polymer in Liquid B may be higher than the content of the electrophilic functional group in the polymer in Liquid A in the composition. In a preferred mode, two or more kinds of combination of Liquid A and Liquid B having different compositions may be used to once form two or more kinds of gel precursors baying different compositions, and the gel precursors may be further cross-linked to obtain a gel having a three-dimensional structure.
The electrophilic functional group contained in the multi-branched polymer in Liquid A is preferably maleimidyl which is an active ester group. When necessary, in addition to the maleimidyl, the polymer may contain N-hydroxy-succinimidyl (NHS), sulfosuccinimidyl, phthalimidyl, imidazoyl, acryloyl, nitrophenyl, or the like. Those skilled in the art can select and employ other known active ester groups as appropriate. Among the multi-branched polymer molecules contained in Liquid A, the composition of the electrophilic functional group may be either the same or different. The composition is preferably the same. In cases where the functional group composition is the same, reactivity with the nucleophilic functional group forming the cross-link is homogeneous, and therefore a gel having a homogeneous spatial structure can be easily obtained.
The nucleophilic functional group contained in the multi-branched polymer in Liquid B is preferably thiol. When necessary, in addition to the thiol, the polymer may contain amino, —CO2PhNO2 (wherein Ph represents o-, m-, or p-phenylene), or the like. Those skilled in the art can select and employ various nucleophilic functional groups as appropriate. Among the multi-branched polymer molecules contained in Liquid B, the composition of the nucleophilic functional group may be either the same or different. The composition is preferably the same. In cases where the functional group composition is the same, reactivity with the electrophilic functional group forming the cross-link is homogeneous, and therefore a gel having a homogeneous spatial structure can be easily obtained.
Preferred specific examples of a multi-branched polymer containing one or more maleimidyl groups in at least one of a side chain(s) and an end(s) and containing a polyethylene glycol as a backbone include, but are not limited to, compounds represented by the following Formula (I), which contains four polyethylene glycol backbone branches, and maleimidyl groups at the ends.
In the Formula (I), each of n21 to n24 may be either the same or different. As the values of n21 to n24 become close to each other, the gel can have a more homogeneous spatial structure, which is preferred because of a higher strength of the gel. n21 to n24 especially preferably have the same value. In cases where the values of n21 to n24 are too high, the gel has a lower strength, while in cases where the values of n21 to n24 are too low, the gel can be hardly formed due to steric hindrance of the compound. Thus, each of n21 to n24 appropriately has a value of from 5 to 300, preferably from 20 to 250, more preferably from 30 to 180, still more preferably from 45 to 115, especially preferably from 45 to 55. The multi-branched polymer in Liquid A has a weight average molecular weight of preferably from 5×103 to 5×104, more preferably from 7.5×103 to 3×104, still more preferably from 1×104 to 2×104.
In the Formula (I), R21 to R24 are linker portions that link the functional groups to the core portion. Although R21 to R24 may be either the same or different, R21 to R24 are preferably the same from the viewpoint of producing a gel having a homogeneous spatial structure and a high strength. In Formula (I), R21 to R24 are the same or different, and examples of R21 to R24 include C1-C7 alkylene, C2-C7alkenylene, —NH—R25—, —CO—R25—, —R26—O—R27—, —R26—NH—R27—, —R26—CO2—R27—, —R26—CO2—NH—R27—, R26—CO—R27—, R26—NH—CO—R27—, and R26—CO—NH—R27—. Here, R25 represents C1-C7 alkylene; R26 represents C1-C3 alkylene; and R27 represents C1-C5 alkylene.
Preferred specific examples of a multi-branched polymer containing one or more thiol groups in at least one of a side chain(s) and an end(s) and containing a polyethylene glycol as a backbone include, but are not limited to, compounds represented by the following Formula (II), which contains four polyethylene glycol backbone branches, and thiol groups at the ends.
In the Formula (II), each of n11 to n14 may be either the same or different. As the values of n11 to n14 become close to each other, the gel can have a more homogeneous spatial structure, which is preferred because of a higher strength of the gel. n11 to n14 especially preferably have the same value. In cases where the values of n11 to n14 are too high, the gel has a lower strength, while in cases the values of n11 to n14 are too low, the gel can be hardly formed due to steric hindrance of the compound. Thus, each of to n11 to n14 has a value of preferably from 25 to 250, more preferably from 35 to 180, still more preferably from 50 to 115, especially preferably from 50 to 60. The multi-branched polymer in Liquid B has a weight average molecular weight of preferably from 5×103 to 5×104, more preferably from 7.5×103 to 3×104, still more preferably from 1×104 to 2×104.
In the Formula (II), R11 to R14 are linker portions that link the fUnctional groups to the core portion. Although R11 to R14 may be either the same or different, R11 to R14 are preferably the same from the viewpoint of producing a gel having a homogeneous spatial structure and a high strength. In Formula (II), R11 to R14 are the same or different, and examples R11 to R14 include C1-C7 alkylene, C2-C7alkenylene, —NH—R15—, —CO—R15—, —R16—O—R17—, —R16—NH—R17—, —R16—CO2—R17—, —R16—CO2—NH—R17—, R16—CO—R17—, R16—NH—CO—R17—, and R16—CO—NH—R17—. Here, R15 represents C1-C7 alkylene; R16 represents C1-C3 alkylene; and R17 represents C1-C5 alkylene.
Here, “C1-C7 alkylene” means an alkylene group which may be branched and which has from 1 to 7 carbon atoms, and means a linear C1-C7 alkylene group, or a C2-C7 all group having one or more branches (having from 2 to 7 carbon atoms including the carbon atoms in the branch(es)). Examples of the C1-C7 alkylene include methylene, ethylene, propylene, and butylene. More specific examples of the C1-C7 alkylene include —CH2—, —(CH2)2—, —(CH2)3—, —CH(CH3)—, —(CH2)3—, —(CH(CH3)2—, —(CH2)2—CH(CH3)—, —(CH2)3—CH(CH3)—, —(CH2)2—CH(C2H5)—, —(CH2)6—, —(CH2)2—C(C2H5)2—, and —(CH2)3C(CH3)2CH2—.
“C2-C7 alkenylene” means a linear or branched alkenylene group having from 2 to 7 carbon atoms, and containing one or more double bonds in the chain. Examples of the C2-C7 alkenylene include divalent groups containing a double bond, which groups are formed by elimination of from 2 to 5 hydrogen atoms from adjacent carbon atoms of the alkylene group.
In the present description, the alkylene group and the alkenylene group may contain one or more arbitrary substituents. Examples of such substituents include, but are not limited to, alkoxy, halogen atoms (any of a fluorine atom, chlorine atom, bromine atom, and iodine atom), amino, mono- or di-substituted amino, substituted silyl, acyl, and aryl. In cases where two or more substituents are contained, those substituents may be either the same or different.
As defined in the present description, in cases where a functional group “may have a substituent(s)”, the type(s), the substitution site(s), and the number of the substituent(s) are not limited. In cases where two or more substituents are contained, the substituents may be either the same or different. Examples of the substituents include, but are not limited to, alkyl, alkoxy, hydroxy, carboxyl, halogen atoms, sulfo, amino, alkoxycarbonyl, and oxo. These substituents may further contain a substituent.
Each of Liquid A and Liquid B forming a gel layer 20a preferably contains an appropriate buffer in addition to the multi-branched polymer component containing a polyethylene glycol as a backbone. Examples of the buffer include phosphate buffer, citrate buffer, citrate-phosphate buffer, acetate buffer, borate buffer, tartrate buffer, Tris buffer, Tris-MCl buffer, phosphate buffered saline, citrate-phosphate buffered saline, and cell culture media. The buffer in Liquid A and the buffer in Liquid B may be either the same or different. Each of the buffer in Liquid A and the butler in Liquid B may be a mixture of two or more kinds of buffers.
In cases where the concentration of the buffer is too low, the buffering capacity in the solution is low, and therefore a gel having a high strength cannot be produced. On the other hand, in cases where the buffer concentration is too high, mixing of the multi-branched polymer component contained in Liquid A and containing a polyethylene glycol as a backbone, with the multi-branched polymer component contained in Liquid B and containing a polyethylene glycol as a backbone, is inhibited. Therefore, a gel having a high strength cannot be produced. Thus, the concentration of the buffer in each of Liquid A and Liquid B is preferably within the range of from 20 mM to 200 mM from the viewpoint of production of a gel having a homogeneous structure and a high strength.
As described above, the gelation time can be controlled by adjusting the pH of the buffer and the concentration of the multi-branched polymer which is contained in each of Liquid A and Liquid B and which contains a polyethylene glycol as a backbone. More specifically, a buffer is used such that the pH of each of Liquid A and Liquid B is preferably adjusted to 5 to 10. The concentration of the multi-branched polymer which is contained in each of Liquid A and Liquid B and which contains a polyethylene glycol as a backbone is preferably adjusted within the range of from 0.3% by mass to 20% by mass. The pH of each of Liquid A and Liquid B is preferably from 6 to 10, and the concentration of the multi-branched polymer which is contained in each of Liquid A and Liquid B and which contains a polyethylene glycol as a backbone is preferably from 1.7% by mass to 20% by mass. The concentration of components derived from multi-branched polymers A and B in a hydrogel is preferably from 0.6% by weight to 8% by weight.
In an acidic solution having a pH of less than 5 in which the concentration of the multi-branched polymer containing a polyethylene glycol as a backbone is less than 0.3% by mass, the nucleophilic functional group is likely to be in a cationic state, leading to repulsion from each other. As a result, reactivity between the nucleophilic functional group in the cationic state and the electrophilic functional group in the other polymer component decreases. On the other hand, in cases where the concentration of the multi-branched polymer containing a polyethylene glycol as a backbone is higher than 20% by mass, the viscosity of a liquid is high, which is not desirable. In an alkaline solution having a pH of more than 10, reactivity between the nucleophilic functional group and the electrophilic functional group is too high, so that the gelation time is abnormally short, Therefore, each polymer cannot be sufficiently dispersed throughout the gel, and the gel becomes fragile as a result. Thus, the solution is not suitable.
Since formation of the gel layer 20a is difficult when the viscosity of Liquid A and Liquid B is too high, specifically, the viscosity of Liquid A and Liquid B at 25° C. is preferably 30 mPa·s or less.
<Molar Ratio between Nucleophilic Functional Group and Electrophilic Functional Group>
Liquid A and Liquid B are preferably mixed together such that the molar ratio between the nucleophilic functional group and the electrophilic functional group is within the range of from 05:1 to 1.5:1. Since the functional groups react with each other at 1:1 to form a cross-link, the closer the mixing molar ratio to 1.1, the more preferred. For obtaining a hydrogel having a high strength, the ratio is especially preferably within the range of from 0.8:1 to 1.2:1.
Liquid A and Liquid B may contain other components, if necessary. The other components are not limited, and may be appropriately selected depending on the purpose. Examples of the other components include culture media, cross-linking agents, pH adjusters, antiseptics, and antioxidants.
The procedure for producing a layered body 1A according to the present embodiment will be described based on
When preparing the layered body 1A, first, as illustrated in
The layered body 1A is prepared by forming the cell layer 10b on top of the gel layer 20a. As illustrated in
Then, a cell suspension 100b for forming the cell layer 10b is added. After the addition, incubation is performed as appropriate, and the culture medium is removed to form the cell layer 10b to obtain the layered body 1A.
A second embodiment of the present invention will be described based on
In this second embodiment of the layered body 1B, the upper gel layer 20b has a barrier property and can protect the cell layer 10b. As described below, by containing a drug or a bin-derived liquid factor in the gel layer 20b, the above-described drug and the like can be released slowly from the gel layer 20b to the cell layer 10b. The layered body 18 can be prepared, for example, by preparing the layered body 1A in accordance with the first embodiment, and adding, Liquid A containing the multi-branched polymer A and Liquid B containing the multi-branched polymer B to the top of the layered body 1A to form the gel layer 20b.
A third embodiment of the present invention will now be described based on
The layered body 1C according to the third embodiment has an advantage that the gel layer 20c is in contact with the bottom of the culture container, and therefore the layered body 1C can be easily separated and collected from the culture container by peeling the gel layer 20c from the bottom of the culture container. The layered body IC can be prepared, for example, by preparing the culture container 40 as in the first embodiment, sequentially or simultaneously adding Liquid A 201 containing the multi-branched polymer A and Liquid B containing the multi-branched polymer B, and allowing the gel layer 20c to gel, and then forming; the cell layer 10a, the gel layer 20a, and the cell layer 10b on the gel layer 20c in the same procedure as in the first embodiment.
Next, a fourth embodiment of the present invention will be described based on
The layered body 1D can be prepared as follows. First, as illustrated in
Next, a seventh embodiment of the present invention will be described based on
The agent or the bio-derived liquid factor that can be contained in the gel layer 21 is not limited, and can be appropriately selected in consideration of an effect on cells, details of a paracrine effect to be investigated, or the like, or two or more agents or bio-derived liquid factors may be contained in combination. Examples of the agent include dimethyl sulfoxide, Y27632, SB431542, dorsomorphine, CHIR99021, IWR-1, ascorbic acid, retinoic acid, forskolin, acetaminophen, 4-aminopyridine, a penicillin antibiotic (such as amoxicillin, ampicillin, or sultamicillin tosylate hydrate), a cephem antibiotic (such as cefcapenpovoxil hydrochloride, cefditoren pivoxil, or cefdinil), a macrolide antibiotic (clarithromycin, erythromycin, or azithromycin), a tetracycline (such as minocycline or doxycycline), a new quinolone (such as levofloxacin, tosfloxacin, or galenoxacin), and an amino acid (such as glutamic acid, methionine, glycine, phenylalanine, or arginine), and examples of the bio-derived liquid factor include NGF, BDNF, NT-3, TNF-α, HGF, IGF, VEGF, EGF, PDGF, TGF-β, IL-1, IL-2, IL-3, 1L4, IL-5, 1L-6, IL-7, IL-8, IFN-α, IFN-β, and IFN-γ.
The layered body 1H can be prepared in accordance with the first embodiment, except that the gel layer 21 is formed by dissolving, suspending, or the like of a drug or a bio-derived liquid factor in at least one of Liquid A and Liquid B to form the gel layer 21.
A ninth embodiment of the present invention will be described based on
The thickness of the layered body according to the first to ninth embodiments is not limited, and can be set to a suitable value to adequately detect a paracrine effect acting between, the cell layers 10a and 10b, specifically, for example, preferably from 0.02 mm to 2 mm, and more preferably from 0.02 mm to 1 mm.
In the first to ninth embodiments, a case in which two cell layers are disposed has been described, but the number of cell layers may be three or more, and a paracrine effect acting between the three or more cell layers can be detected by a layered body in which a gel layer containing a hydrogel is disposed between the three or more cell layers. In this case, the types of cells in the three or more cell layers may all be different, and some (for example, two) of the three or more cell layers may contain cells of the same type.
Various tests can be carried out using the layered body of the present invention as described above. The layered body contains two or more different types of cells in separate cell layers rather than in a mixed state, and an effect on each type of cell when the layered body is stimulated can be detected in isolation. A paracrine effect of a protein secreted into a medium from a cell in one cell layer on cells in another cell layer can be detected with high intensity.
For example, the cell viability M a layered body can be measured by a method including the following steps.
Here, the type of stimulus to a layered body is not particularly limited, and examples of stimuli can include various agents and environmental changes such as temperature. The type of staining reagent and the method of calculating the cell viability by in processing can be appropriately based on previously known methods. Since each cell layer is separated by an intervening gel layer, for example, when each cell layer is observed using a confocal microscope in step (c), cell layers in different positions in the z-axis direction can be observed, and information about living and dead cells in each cell layer can be acquired by image processing.
The expression level of at least one of RNA and protein can be evaluated using the layered body of the present invention. Specifically, the evaluation can be performed by going through the following steps.
Here, the measurement of at least one of RNA and protein expression levels can be performed by appropriately employing a conventional measurement method. Since each cell layer is separated by an intervening gel layer, for example, in step (c), a solution for collecting at least one of an RNA and a protein is added to a cell layer, the solution is collected, and then the gel layer is removed with a pipetman or the like, and the at least one of an RNA and a protein can be collected by the same step for another cell layer under the gel layer.
The cell viability in a layered body can also be measured by the following steps.
Here, examples of the reagent for measuring the cell viability include MTT, WST-1, and WST-8. A cell layer on top of a gel layer is collected, including the gel layer, in a separate culture container, using a pipetman or the like, and a reagent for measuring the cell viability at the same time as a cell layer present on the bottom of the gel layer is added to a culture medium, and the cell viability can be calculated by measuring the absorbance of the culture medium.
Protein expression in a layered body can be evaluated by further going through the following steps.
Here, the luminescent substrate may be selected from various conventionally known substrates, and examples of such substrates include D-luciferin and selenoterazine. Expression of a target protein in each cell layer can be measured based on the luminescence intensity by using cells into which a reporter gene is introduced for cells to be used in each cell layer, and detecting different luminescence wavelengths.
The present invention is described below more concretely by way of Examples and Comparative Examples, However, the present invention is not limited to these Examples.
In 2 mL of a phosphate buffered saline (manufactured by Life Technologies Corporation, hereinafter also referred to as PBS( - - - )), 0.04 g of Tetra-PEG-SH (trade name, SUNBRIGHT PTE-100SH; manufactured by Yuka Sangyo Co., Ltd.) was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm (trade name, Minisart Syringe Filter 175497K; manufactured by Sartorius), to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
In 5 mL of PBS( - - - ), 0.1 g of Tetra-PEG-maleimide (trade name, SUNBRIGHT PTE-100MA; manufactured by Yuka Sangyo Co., Ltd.) was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Terra-PEG-maleimide was 2% by weight.
In an incubator (trade name, KM-CC17RU2; manufactured by Panasonic Corporation; 37° C., environment of 5% by volume CO2), HepG2 cells (JCRB Cell Bank, referred to as “HepG2”), and NIH/3T3 cells (JCRB Cell Bank, referred to as “3T3”) were cultured for 72 hours in a 100 mm dish using Dulbecco's Modified Eagle's Medium (trade name, DMEM (1x); manufactured by Life Technologies Corporation; hereinafter referred to as “DMEM”) supplemented with 10% calf serum (hereinafter also referred to as “serum”).
Green fluorescent dye (trade name, Cell Tracker Green; manufactured by Life Technologies) and orange fluorescent dye (trade name, Cell Tracker Orange, manufactured by Life Technologies Corporation) that were stored frozen was thawed and allowed to warm to room tem endure (25° C.). The dye was then dissolved at a concentration of 10 mmol/L (mM) in dimethyl sulfoxide (hereinafter referred to as “DMSO”). The resulting solution was mixed with serum-free DMEM to prepare serum-free DMEM containing the green fluorescent dye and serum-free DMEM containing the orange fluorescent dye at a concentration of 10 μmol/L (μM). 5 mL of the serum free DMEM containing the green fluorescent dye was added to a dish containing the cultured HepG2,5 mL of the serum-free DMEM containing the orange fluorescent dye was added to a dish containing the cultured 3T3, followed by staining in an incubator for 30 minutes. Thereafter, the supernatant was removed using an aspirator. To the dishes, 5 mL of PBS( - - - ) was added, and then the PBS( - - - ) was removed by aspiration using an aspirator, to wash the surface. After performing two times of the washing operation using PBS( - - - ), 2 mL of 0:05% trypsin-0.05% EDTA solution (manufactured by Life Technologies Corporation) was added to the dishes, and the dishes were then incubated in an incubator for 5 minutes to detach cells from the dishes. After confirmation of the detachment of the cells under a phase contrast microscope (apparatus name, CKX41; manufactured by Olympus Corporation), 4 mL of DMEM supplemented with serum was added to each dish to deactivate the trypsin. The cell suspensions in the dishes were combined and transferred into one 15-mL centrifuge tube, and centrifugation (trade name, H-19FM; manufactured by KOKUSAN Co., Ltd.; 1.2×103 rpm, 5 minutes, 5° C.) was carried out, followed by removal of the supernatant using an aspirator. Thereafter, 2 mL of DMEM supplemented with serum was added to the centrifuge tube, and gentle pipetting was carried out to disperse the cells, to obtain a cell suspension. From the cell suspension, a 20-μL aliquot was taken into an Eppendorf tube, and 20 μL of 0.4% trypan blue staining solution was added to the tube, followed by pipetting. From the stained cell suspension, a 20-μL aliquot was taken and placed on a PMMA plastic slide. The number of cells was counted using a Countess (trade name, Countess Automated Cell Counter; manufactured by Life Technologies Corporation), to determine the number of cells in the suspension.
Matrigel (manufactured by Corning Inc., registered trademark) was mixed well with serum-free DMEM at 1.1 and stored at 4° C. until immediately before use.
A flexiPERM (registered trademark) micro12 reusable (manufactured by SARSTEDT Inc.) was attached to a cover glass, and 2×104 cells of HepG2 suspended in DMEM with serum stained with the green fluorescent dye described above were seeded and incubated in an incubator for at least 16 hours. After the incubation, the culture medium was removed with a pipetman, and 16 μl of Liquid A, which was prepared immediately before use, was added to the culture medium, and Liquid B was added and allowed to gel. After confirming gelation, 50 μl of an extracellular substrate solution was added and incubated at 37° C. for 30 minutes. After the incubation, the extracellular substrate solution was removed, and 2×104 cells of 3T3 suspended in DMEM with serum stained with the orange fluorescent dye were seeded and incubated in an incubator for 24 hours. After the incubation, a layered body was observed under a confocal microscope (FV10i, manufactured by OLYMPUS Corporation), and a three-layered structure including a cell layer 10a, a gel layer 20a, and a cell layer 10b was confirmed (
In 2 mL of a phosphate buffered saline (manufactured by Life Technologies Corporation, hereinafter also referred to as PBS( - - - )), 0.04 g of Tetra-PEG-SH (trade name, SUNBRIGHT PTE-100SH; manufactured by Yuka Sangyo Co., Ltd.) was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm (trade name, Minisart Syringe Filter 175497K; manufactured by Sartorius), to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
In 5 mL of PBS( - - - ), 0.1 g of Tetra-PEG-maleimide (trade name, SUNBRIGHT PTE-100MA; manufactured by Yuka Sangyo Co., Ltd.) was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 2% by weight.
In an incubator (trade name, KM-CC17RU2; manufactured by Panasonic Corporation; 37° C., environment of 5% by volume CO2), HepG2 cells and L190 cells (JCRB Cell Bank, hereinafter referred to as “L190”) were cultured for 72 hours in a 100 mm dish using Dulbecco's Modified Eagle's Medium (trade name, DMEM (1x); manufactured by Life Technologies Corporation; hereinafter referred to as “DMEM”) supplemented with 10% fetal bovine serum (hereinafter also referred to as “FBS”).
To the dishes, 5 mL of PBS( - - - ) was added, and then the PBS( - - - ) was removed by aspiration using an aspirator, to wash the surface. After performing two times of the washing operation using PBS( - - - ), 2 mL of 0.05% trypsin-0.05% EDTA solution (manufactured by Life Technologies Corporation) was added to the dishes, and the dishes were then incubated in an incubator for 5 minutes to detach cells from the dishes. After continuation of the detachment of the cells under a phase contrast microscope (apparatus name, CKX41; manufactured by Olympus Corporation), 4 mL of DMEM supplemented With FBS was added to each dish to deactivate the trypsin. The cell suspensions in the dishes were combined and transferred into one 15-mL centrifuge tube, and centrifugation (trade name, H-19FM; manufactured by KOKUSAN Co., Ltd.; 1.2×103 rpm, 5 minutes, 5° C.) was carried out, followed by removal of the supernatant using an aspirator. Thereafter, 2 mL of DMEM supplemented with FBS was added to the centrifuge tube, and gentle pipetting was carried out to disperse the cells, to obtain a cell suspension. From the cell suspension, a 20-μL aliquot was taken into an Eppendorf tube, and 20 μL of 0.4% trypan blue staining solution was added to the tube, followed by pipetting. From the stained cell suspension, a 20-μL aliquot was taken and placed on a PMMA plastic slide. The number of cells was counted using a Countess (trade name, Countess Automated Cell Counter; manufactured by Life Technologies Corporation), to determine the number of cells in the suspension as in Example 1.
5×104 cells of the L190 suspended in DMEM with serum were seeded in a 24-well multiplate and incubated in an incubator for at least 16 hours (cell layer A). After the incubation, the culture medium was removed with a pipetman, and 16 μl of Liquid A, which was prepared immediately before use, was added to the culture medium, and Liquid B was added and allowed to gel (gel layer A). After confirming gelation, 50 μl of an extracellular substrate solution was added and incubated at 37° C. for 30 minutes. After the incubation, the extracellular substrate solution was removed, and 5×104 cells of HepG2 suspended in DMEM with serum were seeded and incubated in an incubator for 24 hours to form a cell layer B to prepare a layered body (Example 2).
In a 24-well multiplate, 5×104 cells of the L190 suspended in DMEM with serum were seeded, and in an insert (manufactured by Corning), 5×104 cells of the HepG2 suspended in DMEM with serum were seeded. The cells were then incubated in an incubator for at least 16 hours (Comparative Example 1).
To the layered body of Example 2 prepared as described above and HepG2 of the insert in Comparative Example 1, ethanol (manufactured by Wako Pure Chemical Corporation) to a final concentration of 1 mM and acetaminophen (manufactured by Tokyo Chemical Industry Co., Ltd.) to a final concentration of 15 mM were added and incubated for 24 hours. After removal of the culture medium and washing with PBS( - - - ), messenger RNA (hereinafter referred to as “mRNA”) was extracted with RNAeasy (manufactured by QIAGEN) according to the procedure, and complementary DNA (hereinafter referred to as “cDNA”) was synthesized with a SuperScript Kit (manufactured by Thermo Fisher Scientific. Inc.). The expression levels of the type 1 collagen α1 chain were compared by quantitative PCR (hereinafter referred to as “qPCR”) using the synthesized cDNA using the TaqMan probe (manufactured by Thermo Fisher Scientific Inc.). The results are shown in
In 2 mL of a phosphate buffered saline (manufactured by Life Technologies Corporation, hereinafter also referred to as PBS(- - - )), 0.04 g of Tetra-PEG-SH (trade name, SUNBRIGHT PTE-100SH; manufactured by Yuka Sangyo Co., Ltd.) was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm (trade name, Minisart Syringe Filter 175497K; manufactured by Sartorius), to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
In 5 mL of PBS( - - - ), 0.1 g of Tetra-PEG-maleimide (trade name, SUNBRIGHT PTE-100MA; manufactured by Yuka Sangyo Co., Ltd.) was dissolved, and the resulting solution was filtered through a filter having an average pore size or 0.2 μm, to prepare Liquid B which the concentration of Tetra-PEG-maleimide was 2% by weight.
In an incubator (trade name, KM-CC17RU2; manufactured by Panasonic Corporation; 37° C., environment of 5% by volume CO2), SH-SY5Y cells (ECACC, hereinafter referred to as “SH-SY5Y”) and U251MG cells (ECACC, hereinafter referred to as “U251MG”) and human umbilical cord epithelial cells (LONZA, hereinafter referred to as “HUVEC”) were cultured in 100 mm dishes for 72 hours, The culture medium for each cell was culture medium for SH-SY5Y (manufactured by Dainippon Sumitomo Pharma Co., Ltd.), No. 105 medium (manufactured by Dainippon Sumitomo Pharma Co., Ltd.) for U251 MG, and EGM-2 (manufactured by LONZA) for HUVEC.
Matrigel manufactured by Corning Inc., registered trademark) was mixed well with serum-free DMEM at 1:1 and stored at 4° C. until immediately before use.
In a 96-well multiplate (manufactured by Corning Inc.), 2×104 cells of SH-SY5Y were seeded and incubated in an incubator for at least 16 hours. After the incubation, the culture medium was removed with a pipetman, and 16 μl of Liquid A, which was prepared immediately before use, was added to the culture medium, and Liquid B was added and allowed to gel. After confirming gelation, 50 μl of an extracellular substrate solution was added and incubated at 37° C. for 30 minutes. After the incubation, the extracellular substrate solution was removed and 2×104 cells of U251MG were seeded and incubated in an incubator for 2 hours. After confirming that the cells were adhering, the culture medium was removed with a pipetman 16 μl of Liquid A prepared immediately before use was added, and Liquid B was added and allowed to gel. After confirming gelation, 50 μl of the extracellular substrate solution was added and incubated at 37° C. for 30 minutes. After the incubation, the extracellular substrate solution was removed and 2×104 cells of HUVEC were seeded and incubated in an incubator for 24 hours to prepare a layered body (Example 3). A layered body with three cell layers formed only with SH-SY5Y was also prepared (Comparative Example 2). The preparation method was the same as described above.
A frozen WST-1 reagent (manufactured by DOJINDO LABORATORIES) was brought to room temperature and diluted 10 times in EGM-2.
Hydrogen peroxide (Wako Pure Chemical Corporation) was added to the layered body of Example 3 and Example 2 at final concentrations to expose the layered body to 0, 150, and 300 μM, adjusted with PBS ( - - - ) and incubated for 24 hours. After the incubation, the culture medium containing hydrogen peroxide water was removed, 100 μl of the viability measurement reagent was added and incubated at 3° C. for 2 hours. After the incubation, the culture medium was collected from each well and the absorbance was measured with a plate reader (Cytation, manufactured by Biotech Co, Ltd.). The measurement results are illustrated in
In 2 mL of a phosphate buffered saline (manufactured by Life Technologies Corporation, hereinafter also referred to as PBS( - - - )), 0.04 g of Tetra-PEG-SH (trade name, SUNBRIGHT PTE-100SH; manufactured by Yuka Sangyo Co., Ltd.) was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm (trade name, Minisart Syringe Filter 175497K; manufactured by Sartorius), to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
In 5 mL of PBS( - - - ), 0.1 g of Tetra-PEG-maleimide (trade name, SUNBRIGHT PTE-100MA; manufactured by Yuka Sangyo Co., Ltd.) was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 2% by weight.
Liquid A was added in an insert, and then, Liquid B was added in the insert. The amount of Liquid A and the amount of Liquid B to be added was the same, and Liquid A and Liquid B were added so that the gel layer was 1, 2, and 4 mm thick.
Dextrans (manufactured by Thermo Fisher Scientific Inc.) with molecular weights of 570 Da, 10 kDa, and 500 kDa were diluted to 1% by weight in PBS ( - - - ).
600 μl of PBS ( - - - ) was added in a 24well multiplate, and the insert in which the gel layer was prepared to which 300 μl of the fluorescence-labeled molecular weight standard was added was set in the 24-well multiplate. After incubation in an incubator for 2 or 24 hours, PBS ( - - - ) at the bottom of the insert was collected, and the fluorescence intensity was measured by a plate reader (Cytation, manufactured by Biotech Co., Ltd.) for absorbance. The measurement results are illustrated in
In a predetermined amount of a phosphate buffered saline (manufactured by Life Technologies Corporation, hereinafter also referred to as PBS( - - - ) Tetra-PEG-SH (trade name, SUNBRIGHT PTE-100SH; manufactured by Yuka Sangyo Co., Ltd.) was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm (trade name, Minisart Syringe Filter 175497K; manufactured by Sartorius), to prepare Liquid A in which the concentration of Tetra-PEG-SH was 0.7, 1, 2, 4, and 8% by weight.
In PBS( - - - ), a predetermined amount of Tetra-PEG-maleimide (trade name, SUNBRIGHT PTE-100MA; manufactured by Yuka Sangyo Ltd.) was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 0.7, 1, 2, 4, and 8% by weight.
50 μl of Liquid A was dropped into a 96-well multiplate,and be same amount of Liquid B was dropped into the 96-well multiplate. After confirming the gelation, the surface roughness of the gel layer was checked under a microscope. The results are illustrated in Table 1. In Table 1, “Good” indicates that no unevenness was observed in a phase-contrast microscope. As indicated in Table 1, no unevenness was observed at all concentrations at a level where a shadow could be seen on the surface by the phase-contrast microscopy.
In a predetermined amount of a phosphate buffered saline (manufactured by Life Technologies Corporation, hereinafter also referred to as PBS( - - - )),Tetra-PEG-SH (trade name, SUNBRIGHT PTE-100SH; manufactured by Yuka Sangyo Ltd.) was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm (trade name, Minisart Syringe Filter 175497K; manufactured by Sartorius), to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
PBS( - - - ), a predetermined amount of Tetra-PEG-maleimide (trade name, SUNBRIGHT PTE-100MA; manufactured by Yuka Sangyo Co,, Ltd.) was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 2% by weight.
50 μl of Liquid A was dropped onto a glass substrate, and the same amount of Liquid B was dropped onto the glass substrate. After confirming the gelation, the thickness of the gel was measured by confocal measurement. As a result, the thickness of the gel layer was 20 um.
In PBS( - - - ), Tetra-PEG-SH was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
In PBS( - - - ), Tetra-PEG-maleimide was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 2% by weight.
3T3 and 3T3-luciferase cells (ECACC, hereinafter referred to as “3T3-luc”) were cultured in 100 mm dishes in an incubator for 72 hours. The culture medium for each cell was DMEM for both 3T3 and 3T3-luc.
A layered was prepared in the same procedure as in Example 2. For the cell layer A, 3T3-luc was used, and for the cell layer B, 3T3 was used. In order to examine the gel barrier properties, an additional gel layer B was prepared on top of the cell layer B. A layered body without the gel layer B was prepared as a control.
TNF-α (manufactured by Wako Pure Chemical Corporation) was diluted with distilled water. D-luciferin (manufactured by Wako Pure Chemical Corporation) was diluted with Tris buffer at pH7.8.
TNF-α was added to the layered body to a final concentration of 50 ng/ml, and incubated at 37° C. for 3 hours. After three hours, D-luciferin was added to the layered body to a final concentration of 200 μM, incubated at 37° C. for 5 minutes, and the luminescence intensity was measured with a plate reader. The measurement results are illustrated in
In PBS( - - - )), Tetra-PEG-SH was dissolved and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid A in which the concentration of Tetra-PEG-SH was 4% by weight.
In PBS( - - - ) Tetra-PEG-maleimide was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 4% by weight.
Liquid A was added in an insert, and then, Liquid B was added in the insert. The amount of Liquid A and the amount of Liquid B to be added was the same, and Liquid A and Liquid B were added so that the gel layer was 1, 2, and 4 mm thick.
Dextrans with molecular weights of 500 kDa were diluted to 1% by weight in PBS( - - - ).
600 μl of PBS( - - - ) was added to a 24-well multiplate, and the insert in which the gel layer was prepared to which 300 μl of the fluorescence-labeled molecular weight standard solution was added was set in the 24-well multiplate. After incubation in an incubator for 2 and 24 hours, the gel layer was collected, and the fluorescence intensity of the gel was measured using a plate reader. The measurement results are shown in
In PBS( - - - )) Tetra-PEG-SH was dissolved and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
In PBS( - - - ) Tetra-PEG-maleimide was dissolved, and the resulting solution was filtered through a filter having, an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 2% by weight.
SH-SY5Y cells (ECACC, hereinafter referred to as “SH-SY5Y”) and U251MG cells (ECACC, hereinafter referred to as “U251MG”), and human umbilical cord epithelial cells (LONZA, hereinafter referred to as “HUVECs”) were cultured in 100 mm dishes in an incubator for 72 hours. The culture medium for each cell, was medium for SH-SY5Y (Dainippon Sumitomo Pharma Co., Ltd.) for SH-SY5Y, No. 105 medium (Dainippon Sumitomo Pharma Co., Ltd.) for U251MG, and EGM-2 (manufactured by LONZA Co., Ltd.) for HUVEC. Subsequently, a cell suspension was prepared in the same manner as in Example 1.
Matrigel (manufactured by Corning Inc., registered trademark) was mixed well with serum-free DMEM at 1:1 and stored at 4° C. until immediately before use.
For preparing, a layered body (Example 5) with an additional gel layer at the bottom of the cell layer A, flexiPERM (registered trademark) micro12 reusable was attached to a cover glass, 16 μl of Liquid A was added to wells, followed by an equal amount of Liquid B to prepare a gel layer A, and 50 μl of the extracellular substrate solution was added and incubated 37° C. for 30 minutes. After the incubation, the extracellular substrate solution was removed, and 2×104 cells of SH-SY5Y were seeded and incubated in an incubator for 2 hours. After the incubation, the culture medium was removed with a pipetman, 16 μl of Liquid A was added and an equal amount of Liquid B was added and allowed to gel. After confirming gelation, 50 μl of the extracellular substrate solution was added and incubated at 37° C. for 30 minutes. After the incubation, the extracellular substrate solution was removed, 2×104 cells of U251MG were seeded and incubated in an incubator for 2 hours. After the incubation, the culture medium was removed with a pipetman, 16 μl of Liquid A was added and an equal amount of Liquid B was added and allowed to gel. After confirming gelation, 50 μl of the extracellular substrate solution was added and incubated at 37° C. for 30 minutes. After the incubation, the extracellular substrate solution was removed and 2×104 cells of HUVEC were seeded and incubated in an incubator for 24 hours to prepare the layered body of Example 5. On the other hand, a layered body (Example 6) without a gel layer at the bottom was prepared in the same manner as in Example 1.
A scalpel (manufactured by Kai Corporation) was used to separate flexiPERM (registered trademark) micro12 reusable from the side face of a layered body, and the layered body was left in contact with only the side face of the cover glass. The layered body of Example 5 which is in contact with the cover glass by a gel layer was separated from the cover glass with a scalpel in the same manner as the side face. The layered body of Example 6 which is in contact with the cover glass by a cell layer was placed in a 35 mm dish with the cover glass, 5 mL of PBS ( - - - ) was added to the dish, the PBS ( - - - ) was aspirated off with an aspirator, and the surface was washed. After repeating the washing process with PBS ( - - - ) twice, 0.5 mL of 0.05% trypsin-0.05% EDTA solution was added to the dish, and heated in an incubator for 5 minutes to detach the layered body from the dish. The time required for detachment was measured. The results are indicated in Table 2. In Table 2, “Very good” means that the cells were detached without any remaining cells, and “Good” means that 30% of the cells remained. As shown in Table 2, when the gel was placed at the bottom layer, the time required tea detachment was shorter.
In PBS( - - - )), Tetra-PEG-SH was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
In PBS( - - - ), Tetra-PEG-maleimide was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 2% by weight.
A mold for forming a hydrogel layered body support substrate was prepared using dimethylpolysiloxane (manufactured by Dow Chemical Company, hereinafter referred to as “PDMS”). The mold prepared was filled with 75 μl of Liquid A, and then an equal amount of Liquid B was added and allowed to gel. After confirmation of gelation, the hydrogel layered body support substrate was detached from the mold made with PDMS. The substrate was stored in PBS( - - - ) in water until immediately before use.
Cells were cultured and stained in the same manner as in Example 1, and cell suspensions were prepared.
Matrigel (manufactured by Corning in registered trademark) was mixed well with serum-free DMEM at 1:1 and stored at 4°0 C. until immediately before use.
The hydrogel layered body support substrate was placed on a cover glass, and 2×104 cells of HepG2 suspended in DMEM with serum stained with green fluorescent dye were seeded and incubated in an incubator for at least 16 hours. After the incubation, the culture medium was removed with a pipetman, 16 μl of Liquid A prepared immediately before use was added and an equal amount of Liquid B was added and allowed to gel. After confirming gelation, 50 μl of the extracellular substrate solution was added and incubated at 37° C. for 30 minutes. After the incubation, the extracellular substrate solution was removed, 2×104 cells of 3T3 suspended in DMEM with serum stained with orange fluorescent dye were seeded and incubated in an incubator for 24 hours.
The layered body was observed with a confocal microscope. As shown in
In PBS( - - - )), Tetra-PEG-SH was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
In PBS( - - - )Tetra-PEG-maleimide was dissolved, and the resulting solution as filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra PEG-maleimide was 2% by weight.
A layered body support substrate made of hydrogel was prepared the same manner as in Example 7.
Cells were cultured and stained in the same manner as in Example 1, and cell suspensions were prepared.
Matrigel manufactured by Corning Inc., registered trademark) was mixed well with serum-free DMEM at 1:1 and stored at 4° C. until immediately before use.
The hydrogel layered body support substrate was placed on a cover glass, and 2×104 cells of HepG2 suspended in DMEM with serum stained with green fluorescent dye were seeded and incubated in an incubator for at least 16 hours. After the incubation, the culture medium was removed with a pipetman, 16 μl of Liquid A prepared immediately before use was added and an equal amount of Liquid B was added and allowed to gel. After confirming gelation, 50 μl of the extracellular substrate solution was added and incubated at 37° C. for 30 minutes. After the incubation, the extracellular substrate solution was removed, and 2×104 cells of 3T3 suspended in DMEM with serum stained with orange fluorescent dye were seeded. Incubation was carried out in an incubator for 24 hours to prepare a layered body of Example 8.
A layered body of Example 9, in which the top of the cell layer was covered entirely with the hydrogel, was prepared by seeding 2×104 cells of 3T3 suspended in DMEM with serum stained with orange fluorescent dye in the process of preparing the layered body of Example 8, then incubating the cells at 37° C. for 2 hours, then removing the culture medium, adding 16 μl of the Liquid A, and covering the top of the cell layer with an equal amount of the Liquid B.
Examination of drying of layered bodies
The layered body of Example 8, and the layered body of Example 9 in which the top of the cell layer was covered with hydrogel were taken out of the medium and allowed to stand in the room for 30 minutes. In order to see the effect of drying on the cell viability, propidium iodide (manufactured by Sigma Aldrich, hereinafter referred to as “PI”) was diluted to 0.5 ng/ml in a medium, and each layered body was immersed in a PI solution and incubated at 37° C. for 60 minutes. The layered body was observed under a confocal microscope, and the viability was calculated. The measurement results are illustrated in
In PBS( - - - )), Tetra-PEG-SH was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
In PBS( - - - ), Tetra-PEG-maleimide was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 2% by weight,
A layered body support substrate made of hydrogel was prepared in the same manner as in Example 7.
Cells were cultured and stained in the same manner as in Example 1, and cell suspensions were prepared.
Matrigel (manufactured by Coming Inc., registered trademark) was mixed well with serum-free DMEM at 1:1 and stored at 4° C. until immediately before use.
The hydrogel layered body support substrate was placed on a cover glass, and 2×104 cells of HepG2 suspended in DMEM with serum stained with green fluorescent dye were seeded and incubated in an incubator for at least 16 hours. After the incubation, the culture medium was removed with a pipetman, 16 μl of Liquid A prepared immediately before use was added and an equal amount of Liquid B was added and allowed to gel. After confirming gelation, 50 μl of the extracellular substrate solution was added and incubated at 37° C. for 30 minutes. After the incubation, the extracellular substrate solution was removed, 2×104 cells of 3T3 suspended in DMEM with serum stained with orange fluorescent dye were seeded and incubated in an incubator for 24 hours, and a layered body of Example 10 was prepared.
A layered body of Example 11, in which a gel layer is in contact with a culture container, was prepared as follows. The hydrogel layered body support substrate was placed On a cover glass, 16 μl of the Liquid A was added and an equal amount of Liquid B was added and allowed to gel, then 50 μl of an extracellular substrate was added and incubated at 37° C. for 30 minutes, and the extracellular substrate was removed. 2×104 cells of HepG2 suspended in DMEM with serum stained with the green fluorescent dye were seeded and incubated, then the culture medium was removed, 16 μl of the Liquid A was added, an equal amount of Liquid B was added and allowed to gel. 50 μl of the extracellular substrate was added and incubated at 37° C. for 30 minutes, and the extracellular substrate was removed. 2×104 cells of 3T3 suspended in DMEM with serum stained with orange fluorescent dye were seeded and incubated in an incubator for 24 hours to prepare a layered body of Example 11.
The layered body of Example 10 prepared was collected on a cover glass for observation and observed by confocal microscope to see if a layered structure was maintained (
Hoechst 33342 (manufactured by Thermo Fisher Scientific Inc.) was added to the layered body of Example 10 to a final concentration of 5 μg/ml and propidium iodide (Sigma Aldrich) was added to the layered body of Example 10 to a final concentration of 0.5 ng/ml and incubated at 37° C. for 30 minutes.
Images were captured using confocal microscopy and image analysis was performed to calculate the viability. The results are indicated in Table 3. In Table 3, “Good” means that the viability was 75%. The calculated viability was 82%.
In PBS( - - - )), Tetra-PEG-SH was dissolved, mid the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
In PBS( - - - ), Tetra-PEG-maleimide was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 2% by weight.
Preparation of layered body support substrate using hydrogel
A layered body support substrate made of hydrogel was prepared in the same manner as in Example 7.
Cells were cultured and stained in the same manner as in Example 1, and cell suspensions were prepared.
Matrigel (manufactured by Corning Inc., registered trademark) was mixed well serum-free DMEM at 1:1 and stored at 4° C. until immediately before use.
A layered body in which a gel layer is in contact with a culture container was prepared as follows. The hydrogel layered body support substrate was placed on a cover glass, 16 μl of the Liquid A was added and an equal amount of Liquid B was added and allowed to gel, then 50 μl of an extracellular substrate was added and incubated at 37° C. for 30 minutes, and the extracellular substrate was removed. 2×104 cells of 3T3 suspended in DMEM with serum were seeded and incubated, then the culture medium was removed, 16 μl of the Liquid A was added, an equal amount of Liquid B was added and allowed to gel. 50 μl of the extracellular substrate was added and is incubated at 37° C. for 30 minutes, and the extracellular substrate was removed. 2×104 cells of 3T3 suspended in DMEM with serum were seeded and incubated in an incubator for one week to prepare a layered body.
Hoechst 33342 (manufactured by Thermo Fisher Scientific Inc.) was added to the layered body of Example 10 to a final concentration of 5 μg/ml and propidium iodide (Sigma Aldrich) was added to the layered body of Example 10 to a final concentration of 0.5 ng/ml and incubated at 37° C. for 30 minutes.
Images were captured using confocal microscopy and image analysis was performed to calculate the viability. The results was 77% (Table 4). In Table 4, “Good” means that the viability was at least 75%.
PBS( - - - )), Tetra-PEG-SH was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
In PBS( - - - ), Tetra-PEG-maleimide was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 2% by weight.
As a stimulating reagent, a tumor necrosis factor (manufactured by Wako Pure Chemical Corporation, hereinafter referred to as “TNF-α”) was diluted in pure water. As a luminescent substrate reagent, D-luciferin (manufactured by Wake Pure Chemical Corporation) was diluted with 0.5 mol/L of sodium carbonate solution manufactured by Wako Pure Chemical Corporation).
Preparation of Liquid A with Stimulating Reagent
Separately, Liquid A (with TNF-α) was prepared by adding TNF-α to the above prepared Liquid A to a final concentration of 50 ng/ml.
NIH-3T3/NF-B-luc cells (manufactured b Panomics, Inc., hereinafter referred to as “3T3-luc”) were cultured for 72 hours in 100 mm dishes using DMEM with 10% calf serum in an incubator, HepG2 was also cultured in the same manner as in Example 1.
Preparation of Cell suspension
A cell suspension was prepared in the same manner as in Example 1.
Matrigel (manufactured by Corning Inc., registered trademark) was mixed well with serum-free DMEM at 1:1 and stored at 4° C. until immediately before use.
5×104 cells of the HepG2 suspended in DMEM with serum stained with the green fluorescent dye described above were seeded in a 96-well multiplate and incubated in an incubator liar at least 16 hours. After the incubation, the culture medium was removed with a pipetman, and 16 μl of Liquid A or Liquid A (with TNF-α), which was prepared immediately before use, was added to the culture medium, and Liquid B was added and allowed to gel. After confirming gelation, 50 μl of an extracellular substrate solution was added and incubated at 37° C. for 30 minutes. After the incubation, the extracellular substrate solution was removed, and 5×104 cells of the 3T3-luc suspended in DMEM with serum were seeded and incubated in an incubator for four hours to prepare a layered body.
TNF-α was added to the layered body prepared using Liquid A in the gel layer (Example 13) among the above-described layered bodies to a final concentration of 50 ng/ml and incubated in an incubator for two hours. After the incubation, D-luciferin was added to a final concentration of 200 μM, and changes in luminescence intensity were measured every 10 minutes with a plate reader set at 37° C. and 5% CO2 conditions. Similarly, changes in luminescence intensity were also measured for the layered body prepared using Liquid A (TNF-α) as the gel layer (Example 14). The measurement results are indicated in
In PBS( - - - )), Tetra-PEG-SH was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight.
In PBS( - - - ), Tetra-PEG-maleimide was dissolved, and the resulting solution was filtered through a filter having, an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 2% by weight.
Liquid A (with dextran) was prepared by mixing the Liquid A with dextran (molecular weight 570 Da, 10 KDa, and 500 KDa), which was intended for drugs, to reach 1% by weight.
Equal amounts of Liquid A (with dextran) and Liquid B were added to an insert, and a gel layer was prepared by gelation and incubated in wells with PBS ( - - - ) in a microwell plate for 2 hours at 37° C. conditions.
The PBS( - - - ) incubated above was collected, and the fluorescence intensity was measured by a plate reader. The molecular weight of dextran diffused from the gel was calculated from the fluorescence intensity. The results are indicated in Table 5 and
PBS( - - - )), Tetra-PEG-SH was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid A in which the concentration of Tetra-PEG-SH was 2% by weight,
In PBS( - - - ), Tetra-PEG-maleimide was dissolved, and the resulting solution was filtered through a filter having an average pore size of 0.2 μm, to prepare Liquid B in which the concentration of Tetra-PEG-maleimide was 2% by weight.
3T3-luc was cultured in a 100 mm dish with DMEM containing 10% calf serum in an incubator for 72 hours.
For the dish in culture, a supernatant was removed using an aspirator. 5 mL of PBS( - - - ) was added to the dish, and the PBS( - - - ) was aspirated off with an aspirator to wash the surface. After repeating the washing process with PBS( - - - )twice, 2 mL of 0.05% trypsin-0.05% EDTA solution was added to the dish and heated in an incubator for 5 minutes to detach the cells from the dish. After confirming the detachment of the cells by phase contrast microscopy, 4 ml of DMEM with serum was added to the dish. The cell suspension of the dish was transferred to one 15 ml centrifuge tube, and centrifuged, and the supernatant was removed using an aspirator. After the removal, 2 ml of DMEM with serum was added to a centrifuge tube and gently pipetted to disperse the cells to obtain a cell suspension. From the cell suspension, 20 μL of the cell suspension was removed into an Eppendorf tube, and 20 μL of 0.4% trypan blue staining solution was added and pipetted. Twenty μL of the cell suspension was removed from the stained cell suspension and placed on a PMMA plastic slide, and the number of cells in the solution was determined by measuring the number of cells with a Countess.
Matrigel was mixed well with serum-free DMEM at 1:1 and stored at 4° C. until immediately before use.
Hydrogen peroxide water was diluted with PBS( - - - ) to a concentration of 200 mM.
5×104 cells of the 3T3-luc were seeded in a 96-well multiplate and incubated at 37° C. for 24 hours. A layered body of Example 15 from which a culture medium was removed and cells were in direct contact with a gel containing a stimulating reagent was prepared by adding 16 μl of the Liquid A (with hydrogen peroxide), adding 16 μl of the Liquid B and allowing the Liquid to gel, adding 50 μl of an extracellular substrate solution, and incubating at 37° C. for 30 minutes, followed by removal of the extracellular substrate solution, seeding 5×104 cells of the 3T3-luc and incubating at 37° C. for 4 hours.
A layered body of Example 16 which had a structure in which a gel layer for stimulation was sandwiched by a gel layer that did not contain a stimulating reagent was prepared as follows. In the process of preparing the layered body of Example 15, after removing the culture medium, 5 μl of the Liquid A was added, an equal amount of the Liquid B was added to confirm gelation, 16 μl of the Liquid A (with hydrogen peroxide) was added, and 16 μl of the Liquid B was added. Subsequently, 5 μl of the Liquid A was added, an equal amount of the Liquid B was added to confirm gelation, 50 μl of an extracellular substrate solution was added and incubated at 37° C. for 30 minutes. After the incubation, the extracellular substrate solution was removed, and 5×104 cells of the 3T3-luc were seeded and incubated at 37′C for 4 hours to prepare the layered body of Example 16.
Hydrogen peroxide solution was added to a final concentration of 300 μM in each well and incubated for 6 hours at 37° C. and 5% CO2 conditions. After the incubation, D- luciferin was added to a final concentration of 200 μM, and the luminescence intensity was measured for 3 hours with a plate reader set at 37C and 5% CO2 conditions. The measurement results are indicated in
Examples of modes of the present invention include the following <1> to <14>.
contains a drug or a bio-derived liquid factor.
With the layered body or the method using the layered body according to any one of <1> to <14, the conventional problems can be solved to achieve the object of the present invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2019-207225 | Nov 2019 | JP | national |
