Patent Application
20190300835
The present invention relates to culturing of cells in a culture vessel having flexibility, and more specifically to a cell culture method, a cell culture jig and a cell culture apparatus, which can stably form aggregates of cells on a cell culture surface in a flexible cell culture vessel.
In the field of modern therapies led by gene therapy and regenerative therapy, it is practiced to culture desired cells, a desired tissue or the like under an artificial environment. As illustrative cell culture methods at the present time, the following technologies are known.
As a first method, a culture method that uses a well plate can be mentioned as a method suitably usable in laboratories and the like. According to this method, a plate with one or more wells (recessed portions) formed therein is used, and cells and a culture fluid are introduced in the individual well or wells to conduct culturing of the cells. This first method is, however, accompanied by problems that the risk of mixing of foreign matter is high because the well or wells are exposed to the atmosphere and also that the addition to and collection from every well are irksome.
As a second method having improved sealability, on the other hand, there is also such a sealable tray vessel as exemplified in PTL 1. In this method, the upper surface of a tray having recessed portions, in which cells and a culture fluid have been introduced, is sealed with a film. According to this second method, the sealability is enhanced compared with the first method, so that the above-described contamination risk is alleviated.
Even with the second method, however, the contamination risk is considered to be still high because air also flows in and out upon charging and discharging the culture fluid. In addition, the sealable tray vessel has a three-dimensional shape as it is a culture vessel provided with recessed portions, and therefore is bulky and is not considered to be easy in handling.
As described above, many of such current cell culture methods conduct culturing by allowing cells to gather on solid bottoms such as recessed portions or wells. From the rapid progress of regenerative therapy and the like, however, there is an increasing demand for the mass production of cells in recent years.
As a method of mass production that meets such a demand, a method that automatically conducts mass culture of cells in a closed system by using a flexible culture vessel having gas permeability such as that exemplified, for example, in PTL 2. This flexible culture vessel enables to conduct production on a relatively large scale, and therefore permits the mass production of cells. Moreover, the flexible culture vessel is a closed system, and therefore also has a merit that the contamination risk with foreign matter (bacteria, virus and the like) during a culturing period can be reduced. The flexible culture vessel is therefore preferred.
As indicated, for example, in PTL 3, on the other hand, it has been disclosed to the effect that in the culture of stem cells for regenerative therapy such as neural stem cells, cells can be efficiently mass-cultured by forming aggregates of the cells in an initial stage of the culture.
PTL 3 also discloses a technology in which a vessel with cross-sectionally U-shaped, recessed portions, which facilitate the formation of aggregates of cells, formed on one side thereof is used, the aggregates of cells are formed in the recessed portions, and the vessel is then turned upside down to continue the culturing of cells at a cross-sectionally flat surface on an opposite side.
[PTL 1]
JP 509847132
[PTL 2]
JP 534409452
[PTL 3]
JP 4543212B2
However, the above-described well plate, sealable tray vessel and vessel with cross-sectionally U-shaped, recessed portions all involve problems in that they require skill in handling and the quality of cultured cells varies depending on the level of worker's skill. Further, they are fundamentally extremely inadequate for mass production in that a worker must be involved, and are also accompanied by a significant problem in that the risks of operation errors and contamination are still high.
On the other hand, the use of a culture method that uses a flexible culture vessel can substantially eliminate the above-described risk, but there is still a room for development as to how to conduct the mass culture of stem cells for regenerative therapies such as, for example, neural stem cells.
With a view to resolving the above-described problems, the present invention has as objects thereof the realization of a cell culture method, a cell culture jig and a cell culture apparatus, which can culture various kinds of cells economically with high quality and in large quantities by using culture vessels having flexiblity.
To achieve one of the objects described above, a cell culture method of the present invention includes applying a pressure onto a flexible culture vessel filled with cells and a culture fluid and placed on a placement surface, and culturing the cells in the flexible culture vessel with the flexible culture vessel being kept deformed at an outer surface thereof, the outer surface being in contact with the placement surface, under the application of the pressure.
To achieve another one of the objects described above, a cell culture jig of the present invention includes a placement surface configured to exert a deformation on an outer surface of a flexible culture vessel in which cells and a culture fluid are filled, and a pressing lid disposed opposite the placement surface and configured to be movable between a first position, where the pressing lid can hold the flexible culture vessel between the pressing lid and the placement surface while pressing the flexible culture vessel, and a second position, where at least a part of the pressing lid is more remote relative to the placement surface than at the first position.
To achieve a further one of the objects described above, a cell culture apparatus of the present invention includes a placement surface configured to exert a deformation on an outer surface of a flexible culture vessel in which cells and a culture fluid are filled, and a control unit programmed to perform control to deform the outer surface, which is in contact with the placement surface of the flexible culture vessel, by applying a pressure onto the flexible culture vessel after placement of the flexible culture vessel on the placement surface.
To achieve a still further one of the objects described above, a mixing method of the present invention for a culture fluid includes pressing, with a pressing member, a flexible culture vessel filled with cells and the culture fluid and placed on a placement surface, and inserting and moving a mixing member between the pressing member and the flexible culture vessel with the flexible culture vessel being kept deformed at an outer surface thereof, the outer surface being in contact with the placement surface, under the pressing by the pressing member.
To achieve an even further one of the objects described above, a mixing unit of the present invention for a culture fluid includes placement surface configured to exert a deformation on an outer surface of a flexible culture vessel in which cells and the culture fluid are filled, a pressing member that applies a pressure onto the flexible culture vessel placed on the placement surface, a mixing member configured to be insertable and movable between the pressing member and the flexible culture vessel, and a mixing member drive device that drives the mixing member.
To achieve a yet further one of the objects described above, a mixing method of the present invention for a culture fluid includes pressing, with a pressing member, a flexible culture vessel filled with cells and the culture fluid and aced on a placement surface, and rocking the pressing member to perform mixing of the culture fluid with the flexible culture vessel being kept deformed at an outer surface thereof, the outer surface being in contact with the placement surface, under the pressing by the pressing member.
According to the present invention, it is possible to mass-culture cells of reduced contamination risk and high quality by using a culture vessel having flexibility while enabling to form aggregates of cells as needed.
Referring to the drawings as needed, a description will hereinafter be made specifically about cell culture methods, cell culture and cell culture apparatus of the present invention. For the sake or convenience of the description, an X-direction, F-direction and Z-direction will be individually defined, in the following description, but are not intended to limit or restrict the scope of the right of the present invention.
Firstly, a first embodiment of the present invention will be described with reference to
The cell culture apparatus 1 includes at least a stage 2 and a control unit 13. The stage 2 has a placement surface 2a in which one or more depressions 2b are formed. The control unit 13 is programmed to perform control so that subsequent to placement of a flexible culture vessel FP on the placement surface 2a, a pressure is applied onto the flexible culture vessel FP to form recessed and projected portions, which conform to the depressions 2b, in and on an outer surface FPs. The cell culture apparatus 1 is used to culture cells C, which are filled in the flexible culture vessel FP, in a frame 11 controlled at an appropriate temperature (for example, 37° C.), carbon dioxide gas concentration (for example, 5% to 10% CO2 concentration) and humidity (for example, approximately 95%).
The term “flexible culture vessel FP” as used herein means a culture vessel, which is formed in the form of a pouch by using, as a material, a film-based, soft packing material and has flexibility. The flexible culture vessel FP has gas permeability suitable for the culture of the cells C, and preferably has transparency at a part or the entire part thereof to permit visual examination of its contents.
As depicted by way of example in
The base layer f1 and the inner layer f2 are formed with a material provided with high gas permeability, heat sealability and transparency. On the other side, the inner layer f2 is formed with a material provided with low cytotoxicity in addition to the properties described above. As such a material, a polyethylene-based resin such as, for example, linear low density polyethylene (LLDPE), very low density polyethylene (VLDPE) or ultra low density polyethylene (ULDPE), low density polyethylene (LDPE), or a blend of two or more of them can be used.
As the outer layer f3, on the other hand, a polyethylene-based resin having a density of from 0.886 to 0.93 g/cm3 is suitable. The outer layer f3 may be omitted as desired.
For the more detailed structure of the flexible culture vessel FP suited for the present embodiment, a reference may be made, for example, to JP 5344094B2 and the like.
No particular limitation is imposed on the cells C to be cultured in the flexible culture vessel FP, but cells for the culture of which the formation of cell aggregates effective (induced pluripotent stem cells (iPS cells), embryonic stem cells (ES cells), neural stem cells, hepatocytes, corneal stem cells, islet cells, and so on) are particularly suited.
Further, the culture fluid as a medium to be supplied to the flexible culture vessel FP can be also selected, as desired, depending on the cells C to be cultured.
Concerning the cell culture apparatus 1 in which the culture of the cells C is performed using the flexible culture vessel FP with such cells C and culture fluid filled therein, details of individual elements which are also included therein will be described hereinafter.
The stage 2 is a plate member on which the flexible culture vessel FP to be described subsequently herein is to be placed, and is formed, for example, from a metal, a hard resin or the like. In
The placement surface 2a is a planar surface of the stage 2, on which the flexible culture vessel FP is placed. The planar surface has a function to exert a deformation on an outer surface of the flexible culture vessel FP. The plural depressions 2b are formed in the planar surface.
The depressions 2b are locations depressed from the placement surface 2a, and, in the present embodiment, have the shape of a through-hole that extends from the placement surface 2a of the stage 2 to a back surface on the opposite side of the stage 2. Owing to the arrangement of one or the plural number of depressions 2b in the placement surface 2a as described above, one or the like plural number of recesses and projections are formed in and on the placement surface 2a. The “depressions” as described in the present invention are only required to be in such a shape that the outer surface FPs, which is to be described subsequently herein, of the flexible culture vessel FP is formed into a recessed or projected form as a result of an extension of the outer surface FPs from the placement surface 2a into the depressions 2b. The depressions 2b are not necessarily required to extend through the stage 2, and may be formed as recessed portions.
Stage supporting posts 3 are metal or resin members that support the stage 2, and an observation device 7, a stage device 12 and the like can be accommodated in a space inside the stage supporting posts 3. In the present embodiment, the stage supporting posts 3 are disposed in such a way that the stage 2 is supported at four corners thereof by the totally-four stage supporting posts 3.
A pressing member 4 is disposed opposite the flexible culture vessel FP, and is a member of a three-dimensional shape that a bottom surface, which presses the flexible culture vessel FP, is, for example, a planar surface. As the material of the pressing member 4, a transparent resin such as acrylic resin is used in the present embodiment. The shape of the pressing member 4 in plan may desirably be greater than at least the flexible culture vessel FP, but its size or the like is not particularly limited and may be smaller than the flexible culture fluid FP insofar as a desired pressure can be applied to the flexible culture vessel FP. If a lighting device 8 to be described subsequently herein is not needed, the material of the pressing member 4 is not required to be a transparent resin, and the pressing member 4 may be formed, for example, of a metal.
The above-mentioned bottom surface of the pressing member 4 is not absolutely required to be planar. It is possible to use, for example, one having a three-dimensional that a bottom surface is a curbed surface (i.e., a surface that is projected in the -Z-direction (downwardly)). In addition, to promote the exchange of gas flexible culture vessel FP, one or more holes may be provided through the bottom surface (i.e., the surface on the side opposite the placement surface 2a) of the pressing member 4.
Pressure applying devices 5 are connected to the pressing member 4 via piston rods 5a and connecting links 5b, and cause the pressing member 4 to advance and retract relative to the stage 2 under control of the control unit 13 to be described below. As the pressure applying devices 5 and the piston rods 5a, known piston pumps or the like can be applied.
In the present embodiment, the piston rods 5a are connected approximately to the four corners of the pressing member 4 via the connecting links 5b, whereby the pressing member 4 can be lowered (moved in the -Z-direction) while maintaining the bottom surface (the surface on the side opposite the stage 2) of the pressing member 4 in a horizontal position. As will be described below, the individual piston rods 5a are configured to be independently controllable so that the special orientation of the bottom surface of the pressing member 4 can be adjusted, as needed, during the descend of the piston rods 5a.
The numbers of the piston rods 5a and connecting links 5b for each pressing member 4 are not limited to four described above, and the piston rod(s) 5a and the connecting link(s) 5b may be included in one or more sets. In the drawings, the pressure applying devices 5 are depicted as discrete devices, but a single pressure applying device 5 may be used in common insofar as it can independently control the individual piston rods 5a.
A vessel connection port 6 is disposed for connection with the port FP1 of the flexible culture vessel FP. In the present embodiment, the opening and closure of the vessel connection port 6 is controlled by the control unit 13. According to this control, a fresh supply of the medium is fed via a tube T to the flexible culture vessel FP placed on the placement surface 2a, and the used medium is collected from the flexible culture vessel FP via the tube T.
In the following, a description will be made taking an example in which a medium supply tank 9 and a medium collection tank 10 to be described subsequently herein are disposed independently of the flexible culture vessel FP, but the first embodiment is not limited to this example. Described specifically, the medium supply tank and the medium collection tank may be individually incorporated as dedicated bags in the flexible culture vessel FP, and the flexible culture vessel FP may be replaced together with the dedicated bags incorporated therein per every cycle of culture of the cells C.
In the present embodiment, the vessel connection port 6 is provided with an identification tag reading part (not depicted) to enable the identification of the contents of the flexible culture vessel FP to be connected to the vessel connection port 6. Described specifically, an identification tag is attached to a part (near the port FP1 or the like) of the flexible culture vessel FP, and information of the kind of the cells C, the composition of the culture fluid, and the like filled in the vessel is included in the identification tag. As a consequence, the control unit 13 can perform, for example, appropriate culture processing such as the initiation, stop and the like of a culturing operation based on the information read at the identification tag reading part. The term “culturing operation” as used in the present embodiment embraces temperature control and moisture control around the flexible culture vessel FP, operation control of the pressing member 4 (adjustment of the pressing force, and the like), the supply and collection of the medium, and so on. No particular limitation is imposed on the identification tag to be used in the present embodiment, and a known identification member may be used. However, a bar code or quick response (QR) code, a radio-frequency (RF) tag or integrated circuit (IC) tag, or the like is a suitable example.
The observation device 7 is a device that observes the state of the cells C in the flexible culture vessel FA via an object lens or the like, and as the observation device 7, an optical microscope, fluorescence microscope with a charge-coupled device (CCD) and a complementary metal-oxide semiconductor (CMOS) image sensor mounted thereon, or the like can be exemplified. The observation device 7 is arranged below the stage 2 such that the observation device 7 can be moved in horizontal directions on the stage device 12 to be described below. One observation device 7 is arranged for every stage 2 in the present embodiment, but without being limited to such an arrangement, a plurality of observation devices 7 may be arranged for every stage 2 such as an arrangement pattern that a plurality of observation devices 7 are arranged corresponding to the positions of the depressions 2b. Further, the observation device 7 is movable in the horizontal directions, and in addition, is displaceable about the direction of an X-axis (θX-direction) and the direction of a Y-axis (θY-direction), whereby the special orientation of the observation device 7 during an observation can be adjusted. The observation device 7 is configured to permit capturing an image of a region observed as needed, and storing the captured image data in a memory or the like (not depicted).
The lighting device 8 is a device that generates light needed when the observation device 7 observes the state of the cells C in the flexible culture vessel FP, and is arranged in a pair with the observation device in the present embodiment. As the lighting device 8, various known light sources may each be used, but a mercury vapor lamp or the like which generates excitation light may be exemplified, for example, when the observation device 7 is a fluorescence microscope. In the present embodiment, the lighting device 8 is arranged on a side opposite the observation device 7 relative to the stage 2 (placement surface 2a), but without being limited to this arrangement, the lighting device 8 may also be arranged on the same side as the observation device 7 relative to the stage 2 (placement surface 2a). Further, the lighting device 8 may be configured to be movable in horizontal directions while keeping the optical axis of the lighting device 8 in conformity with that of the observation device 7 by a drive mechanism such as an XY stage 12a as depicted in
The medium supply tank 9 is a receptacle in which a medium (such as a culture fluid) required for the culture of the cells C is stored. The control unit 13 controls a valve Va and a pump P, thereby performing control to supply the medium, which is stored in the medium supply tank 9, to the flexible culture vessel FP via the tube T. A temperature control device (not depicted) is mounted on the medium supply tank 9, and by this temperature control device, the inside of the medium supply tank 9 is kept at a temperature where the medium can be maintained in freshness and quality.
The medium collection tank 10 is a receptacle for collecting the medium the role of which has been completed through its use for the culture of the cells C in the flexible culture vessel FP. The control unit 13 controls another valve Va and the pump P, thereby performing control to collect the unnecessary medium (culture fluid) from the flexible culture vessel FP via the tube T. The medium collected in the medium collection tank 10 may be discarded, or after subjected to an appropriate treatment, may be fed to the medium supply tank 9 for its reuse.
If the medium supply tank 9 and the medium collection tank 10 are in the form of the above-mentioned dedicated bags, on the other hand, pinch valves and a tube roller pump (peristaltic pump) are suited as the valves Va and as the pump P, respectively, so that the culture fluid does not come into contact with the valves Va and the pump P.
The frame 11 is a frame structure forming an accommodation space in which the above-described individual members needed for the culture of the cells C, such as the stage 2 and pressing member 4, are disposed. The frame 11 in the present embodiment is formed of a metal such as stainless steel or aluminum, and as depicted in
The stage device 12 includes an XY stage 12a that drives the above-described observation device 7 along two axes in direction parallel to the placement surface 2a under the control of the control unit 13. As the XY stage 12a, it is possible to apply a known two-axis drive mechanism such as, for example, a feed screw mechanism, linear ball guideway, a cross roller guideway, or a planar motor system.
Further, the stage device 12 further includes a Z stage 12b for adjusting the focal point of the observation device 7. As the focal point may vary depending on the film thickness and the degree of bulges of the above-mentioned recessed portions of the flexible culture vessel FP in the present embodiment, the focal point-adjusting Z stage 12b is particularly effective for realizing high-precision observations. No particular limitation is imposed on the specific adjusting method of the focal point. For example, however, a contrast detection method using image processing may be mentioned as a non-limiting method. The Z stage 12b is disposed below the observation device 7, and moves the observation device 7 in a direction perpendicular to the placement surface 2a (Z-direction). As the Z stage 12b, a desired one of various known mechanisms such as those including one or more screws or air cylinders can be applied. The Z stage 12b may be disposed on the XY stage 12a, or may be moved up and down in the Z-direction together with the XY stage 12a. As a further alternative, the XY stage 12a and the Z stage 12b may be integrated into a stage configuration that enables a drive along at least three axes.
If the lighting device 8 is also arranged below the stage 2 as described above, the lighting device 8 may also be driven along two axes the stage device 12.
An air-conditioning unit U is arranged on the side of the rear board 11d as depicted in
The control unit 13 is, for example, a computer provided with a memory, in which predetermined programs are stored, and a central processing unit (CPU) having arithmetic functions, and is provided with functions to perform control of the above-described individual members to totally govern the culture of the cells C.
In the drawings, the control unit 13 is arranged on the frame 11 for descriptive purposes, but its arrangement is not limited to this illustrative location. For example, the control unit 13 may be arranged in such a fashion that it is assembled together with a display on the side board 11b, or may be in the form of a personal computer or laptop computer wiredly or wirelessly connected with the above-described individual members as control targets.
With reference to
Now, the cell culture method of the present embodiment is primarily characterized by applying a pressure to a culture vessel which is filled with cells and a predetermined culture fluid, has flexibility and is placed on a placement surface having one or more depressions, and culturing the cells in the flexible culture vessel with the flexible culture vessel being kept deformed at an outer surface thereof, the outer surface being in contact with the placement surface, under the pressure so applied.
Described specifically, as depicted in
If the temperature control unit is mounted on the stage 2, the temperature of the culture fluid or the like in the flexible culture vessel FP may be adjusted by contrail temperature of the stage 2 is step 1 onwards.
As depicted in
As depicted in
When the recessed and projected portions have been formed in and on the outer surface FPs of the flexible culture vessel FP by the pressing member 4 the cells C dispersed or suspended in the flexible culture vessel FP begin to gather in the recessed portions (the regions drawn into the depressions 2b). In the present embodiment, the cells C are cultured with the recessed and projected portions, which conform to the depressions 2b in the placement surface 2a, being formed in and on the outer surface of the flexible culture vessel FP as described above. The flexible culture vessel FP is left stand such that the pressed state of the flexible culture vessel FP the pressing member 4 continues for a time required to allow all the cells to precipitate, for example, for from several minutes to several tens of minutes. As a consequence, the cells C suspended in the culture fluid have all been allowed to precipitate after the standing.
As depicted in
In step 3 and step 4, the pressing force by the pressing member 4 may be adjusted by changing it based on the state of the outer surface FPs of the flexible culture vessel FP, the degree of aggregation of the cells C, and the like as acquired from the observation device 7. As is understood from the foregoing, the observation device 7 in the present embodiment is configured to permit observations of the inside and outer surface of the flexible culture vessel FP with the pressing by the pressing member 4 being kept applied to the flexible culture vessel FP. Further, the observation device 7 in the present embodiment is configured to permit the observation of the inside of the flexible culture vessel FP via the depressions 2b.
As depicted in
By leaving the flexible culture vessel FP to stand for the predetermined time in the state of step 5, the culture of the cells proceeds further, and after the elapse of the predetermined time, the culture of the cells ends. Subsequent to the end of the culture of the cells, the worker opens the front doors 11c and takes out the flexible culture vessel FP from the placement surface 2a, whereby the work is completed.
Here, the reason for releasing the applied pressure (pressing force) during the culture of the cells C is as will be described next.
Depending on the kind of the cells C to be cultured, the efficiency of culture is substantially improved when aggregates are formed. If the recessed portions remain, on the other hand, inconvenience can be assumed to arise during the culture.
Described more specifically, it should also be assumed that during the culture of the cells C, a need arises to improve the freshness of the culture fluid in the vessel by replacing a portion of the culture fluid and also to allow gas, which permeates into the vessel (such as carbon dioxide and oxygen), to efficiently diffuse in the vessel. However, if the recessed and projected portions remain in and on the outer surface FP of the flexible culture vessel FP and especially when the amount of the medium (the culture fluid or the like) is small, no sufficient clearance can be assured to remain between the bottom surface of the vessel and the opposite surface at the projected portions, presumably leading to a potential problem that the circulation of the culture fluid, the diffusion of the gas, and the like may stop.
In the present embodiment, it is, therefore, configured, as depicted in
If it is desired to realize efficient circulation and diffusion of the culture fluid and gas without using this method, it may be contemplated, for example, to transfer the aggregates C′ into a large vessel. This approach is, however, accompanied by various risks as will be described below. If work is performed to transfer the aggregates C′ into a vessel having a large area, it is necessary to use a pipette or the like. Various risks, therefore, arise such that the aggregates C′ may break up due to strong mixing of the culture fluid and a physical stress such as a shear force may be applied to each cell C to give deleterious effects on the subsequent culture.
However, the use of such a method as in the present embodiment makes it possible to enjoy effects, which are substantially equivalent to those available from the transfer of the aggregates C′ to the large vessel, without being accompanied with the above-mentioned risks by simply removing the pressing by the pressing member 4.
During or in parallel with step 1 to step 5 described above, a fresh supply of the medium may be delivered as needed into the vessel from the medium supply tank 9, or the used medium may be collected from the vessel into the medium collection tank 10.
The observations of the cells C, their aggregates and the like by the observation device 7 may be conducted continuously or intermittently during step 1 to step 5. As an alternative, the aggregates and the like at plural different locations among the recessed and projected portions of the flexible culture vessel FP may be sequentially observed by driving the observation device 7 with the stage device 12 as needed.
As the flexible culture vessel FP is reduced in the risk of contamination and its handling is easy as described above, a portable cell culture jig was adopted to hold the flexible culture vessel FP in the present embodiment. An objective of the use of this cell culture jig is to realize the culture of cells in mode, which is more efficient and is reduced in contamination risk, while retaining the advantage that it can be carried by hands like a conventional flask or well plate.
Described specifically, the cell culture jig of the present embodiment is primarily characterized by including a placement surface that exerts a deformation on an outer surface of a flexible culture vessel in which cells and a culture fluid are filled, and a pressing lid disposed opposite the placement surface and capable of moving between a first position, where the flexible culture vessel can be held between the pressing lid and the placement surface while pressing the flexible culture vessel placed on the placement surface, and a second position where at least a part of the pressing lid is more remote relative to the placement surface than at the first position.
According to this cell culture jig, it is possible to perform transfers the flexible culture vessel FP, for example, among a CO2 incubator that is commonly used in the culture of cells, a clean bench where the addition and replacement of a culture medium are conducted, and a microscope that performs observations of cells in the culture vessel, while holding the flexible culture vessel FP.
Described specifically, as depicted in
As depicted in
The pressing lid 26 is connected with an upper lid 24 via bars 25, and can be moved toward or away relative to the upper lid 24 while its spatial orientation is maintained by bars 25. Also, the upper lid 24 is connected with the base 21 via a hinge 23, and is configured to be turnable about the hinge 23 as an axis.
Therefore, upon accommodating the flexible culture vessel FP in the cell cult 20, the flexible culture vessel FP is firstly placed on the placement plate 22 with the upper lid 24 being opened via the hinge (the pressing lid 26 assumes the second position), and the upper lid 24 is then closed until the upper lid 24 is locked relative to the base 21 by a locking mechanism (not depicted) (at least part of the pressing lid 26 moves toward the placement plate and assumes the first position).
At this time, the pressing 26 moves toward the placement plate 22 via the bars 25 along the movement of the upper lid 24, whereby pressing force is applied by the pressing lid 26 onto the flexible culture vessel FP. Here, the pressing force can be produced by the mass of the press lid 26, or can be produced by locking the pressing lid 26 with the locking mechanism (not depicted) with the pressing lid 26 being kept pressed against the flexible culture vessel FP.
The worker then performs the work of culturing the cells in the flexible culture vessel FP by carrying the cell culture jig 20, with the pressing force being applied to the flexible culture vessel FP by the pressing lid 26, into the CO2 incubator by hands or the like.
The cell culture jig 20 of the present embodiment may also be used, example, in the cell culture apparatus 1 instead of the mode in which it is used in the CO2 incubator. If the cell culture jig 20 is used in the cell culture apparatus 1, the stage 2 may be omitted. In this case, a structure that the base 21 and free ends of the stage supporting posts can be connected and fixed together is preferred.
On the other hand, the cell culture jig 30 includes, as depicted in
Upon placing the flexible culture vessel FP on the placement surface of the lower lid 31, the pressing lid 33 is moved to the second position as depicted on a left side of
After the flexible culture vessel FP has been placed on the placement surface, parallel links 32 are driven to press the pressing lid 33 against the flexible culture vessel FP as depicted on a right side of
The lower lid 31 and the pressing lid 33 are next locked together by the locking mechanism (not depicted) while maintaining the pressing force against the flexible culture vessel FP by the pressing lid 33 (the pressing lid 33 moves toward the placement surface and assumes a first position).
A mode which the flexible culture jig 30 is used in the incubator or the cell culture apparatus 1 is similar to the above-mentioned case of the cell culture 20, and therefore its description is omitted.
In the first embodiment described above, the example in which two stages 2 are disposed side side in the Y-direction is presented in
Moreover, a plurality of flames 11 in each of which the stage 2 is accommodated may be disposed side by side in a height direction (the Z-direction). As an alternative, the interior of the frame 11 may be divided into plural compartments in the height direction, and the stage 2 and the pressing member 4 may be disposed in each of the compartments so divided.
Next, a description will be made about a second embodiment of the present invention with reference to
Differences of the second embodiment from the first embodiment reside, for example, in that a pressure to be applied onto the flexible culture vessel FP is produced by a negative pressure source 14 via a stage 2′ and also in that an observation device is arranged above the stage 2′.
These differences from the first embodiment will hereinafter be described primarily, and the same configurations and functions as in the first embodiment will be identified by the same symbols and their description will be omitted unless needed (this will equally apply to third to fifth embodiments and modifications 1 and 2 to be described subsequently herein).
As depicted in
In addition, the cell culture apparatus 1 of the present embodiment is provided with a negative pressure generator that produces, via the depressions 2′b, a suction force to the flexible culture vessel FP placed on the placement surface 2′a of the stage 2′. This negative pressure generator includes the negative pressure source 14 and pipings 14a that connects the negative pressure source 14 and the flow channels 14b of the stage 2′ together.
As the negative pressure generator is disposed below the stage 2′ as described above, the observation device 7′ in the present embodiment is arranged above relative to the stage 2′ and is configured to be movable in the X-direction or Y-direction. The present embodiment does not include the pressing member 4, so that a lighting device 8′ is also arranged side by side with the observation device 7′.
By the second embodiment described above, the outer surface FPs of the flexible culture vessel FT is also formed into a shape conforming to the depressions 2′b (one or more recessed and projected portions) under the application of a negative pressure by drawing the outer surface FPs of the flexible culture vessel FP by using the negative pressure generator without using the pressing member, whereby recessed and projected portions conforming the depressions 2′b of the stage 2′ can be also formed in and on the outer surface FPs.
In the present embodiment, the depressions 2′b are internally depressurized using the negative pressure source 14. However, a positive pressure may be applied to the flexible culture vessel FP via the depressions 2′b by using a positive pressure source instead of the negative pressure source.
Next, a description will be made about a third embodiment of the present invention with reference to
Differences of the third embodiment from the first embodiment reside, for example, in that a stage 2″ is formed of a transparent material such as acrylic resin and also in that depressions 2″b of the stage 2″ are bottomed recessed portions rather than through-holes.
The observation device 7 in the present embodiment can observe aggregates or the like of cells C in the flexible culture vessel FP via the transparent stage 2″, and moreover can also observe a medium on a placement surface 2″a, suspended cells C and the like as needed.
In other words, the observation device 7 can observe and capture images at all locations of the flexible culture vessel FP in the present embodiment.
In the present embodiment, the depressions 2″b are formed as the bottomed recessed portions rather than through-holes. The present embodiment is not limited to this form, but the depressions 2″b may be formed as through-holes.
According to the third embodiment described above, it is possible to determine whether cells C locally exist at a location or locations other than the recessed portions in the flexible culture vessel FP, whereby the cells C are efficiently allowed to gather in the recessed portions and to form aggregates there.
Next, a description will be made about a fourth embodiment of the present invention with reference to
Differences of the fourth embodiment from the first embodiment reside, for example, in that a stage 2″ is formed of a transparent material such as acrylic resin, in that depressions 2″b of the stage 2″ are bottomed recessed portions rather than through-holes, and also in that the pressing member 4 has been omitted and a pressure regulator 15 is included.
Described specifically, as depicted in
Since the depressions 2″b in the present embodiment are the recessed portions, on the other hand, the recessed portions exist as closed spaces when the flexible culture vessel FP is placed on a placement surface 2″a.
Therefore, the pressure in the space SP becomes higher than that of the closed spaces upon application of a pressure by the pressure regulator 15, whereby recessed and projected portions conforming to the depressions 2″b are formed in and on the outer surface FPs of the flexible culture vessel FP.
According to the fourth embodiment described above, the flexible culture vessel FP is pressed in a non-contact fashion instead of being physically pressed by the pressing member 4 or the like, so that the desired recessed and projected portions can be formed while inhibiting damage to the flexible culture vessel FP if at all possible.
Next, a description will be made about a fifth embodiment of the present invention with reference to
Differences of the fifth embodiment from the first embodiment reside, for example, in that the present embodiment includes a mixing unit and a mixing method for a culture fluid and also in that the present embodiment has a mixing member 16 insertable between the flexible culture vessel FP pressed by the pressing member 4 and the pressing member 4, and mixing member driving devices 17 that drive the mixing member 16.
As described above concerning t e respective embodiments, the cells C in the culture fluid in the flexible culture vessel FP can exist as the aggregates C′. Here, for the purpose of effectively supplying nutrients to the cells C or a like purpose, an operation is needed to mix the culture fluid in the flexible culture vessel FP at every predetermined time. As the aggregates C′ have been formed in the flexible culture vessel FP at this time, it is desired to mix only the culture fluid without causing the aggregates C′ to move if at all possible.
The mixing unit and the mixing method to be described below have, therefore, been adopted for the culture fluid in the present embodiment.
As depicted in
As the placement surface, it possible to use the placement surface corresponding to the stage (stage 2, stage 2′ or stage 2″′) disclosed above with respect to any one of the first embodiment to the fourth embodiment.
The mixing member 16 has a function that it is inserted and moved between the pressing member 4 and the flexible culture vessel FP while the state of pressing against the flexible culture vessel FP by the pressing member is maintained. No particular limitation is imposed on the material of the mixing member 16, and a metal material such as stainless steel or a resin material such as plastics can be used, for example. To a surface of the mixing member 16 where it comes into contact with at least the flexible culture vessel FP, desired one of various surface treatment or processing such as, for example, coating with a fluorine-containing material and polishing may be applied to provide the surface with reduced friction. From the viewpoint of reducing the friction caused by contact between the pressing member 4 and the mixing member 16, the above-described surface treatment or processing may also be applied to a surface of the mixing member 16 where the mixing member 16 opposes the pressing member 4.
Described more specifically, as also depicted in
The mixing member driving devices 17 have functions to support the mixing member 16 and also to allow the mixing member 16 to move in an inserting and moving direction (the Y-direction) between the flexible culture vessel FP and the pressing member 4. As each mixing member driving device 17, desired one of various known power mechanisms can be applied. Illustrative may be a gas-actuated cylinder, a rack and pinion mechanism, a ball screw linear motion mechanism, or a linear motion mechanism which uses magnets.
As depicted in
The mixing member driving devices 17 are not absolutely needed to be mounted on the pressing member 4, and may be disposed, for example, on the side of the placement surface. If the mixing member driving devices 17 are disposed at locations other than the pressing member 4, it is preferred to dispose the mixing member 16 and the mixing member driving devices 17 via resilient members (spring mechanisms or the like) which are displaceable in the Z-direction, so that the mixing member 16 and the mixing member driving devices 17 can follow displacements of the pressing member 4 in the Z-direction.
The mixing member driving devices 17 may support the mixing member 16 via known lift mechanisms such as pistons so that the mixing member 16 can ascend and descend (can move in the Z-direction). As a consequence, the position of the mixing member 16 in the Z-direction can be adjusted independently from movements of the pressing member 4, for example, under the control of the control unit 13.
Using
Described specifically, the mixing method of the present embodiment for the culture is primarily characterized by placing, on the placement surface, the flexible culture vessel FP with cells C and culture fluid filled therein, pressing the flexible culture vessel FP with the pressing member 4, and then inserting and moving the mixing member 16 between the pressing member 4 and the flexible culture vessel FP with the outer surface, which is in contact with the placement surface, of the flexible culture vessel FP being kept deformed under the pressing by the pressing member 4.
Firstly, an initial position of the mixing member 16 is depicted in
However, the above-described initial position is not limited to the end port or of the pressing member 4 or the placement surface, and may be another position, for example, an end portion of the flexible culture vessel FP insofar as the internal pressure of the flexible culture vessel FP does not vary.
As depicted in
In the present embodiment, following the above-described insertion (movement) of the mixing member 16, a localized flow of the culture fluid occurs in the flexible culture vessel FP at only a region around its contact with member 16, and this localized flow of the culture fluid shifts in the inserting and moving direction (the Y-direction) as the mixing member 16 moves. As this flow of the culture fluid is localized, no effect is given to the aggregates C′ settled on the bottom of the flexible culture vessel FP.
As a consequence, aggregates C′ which exist in the recessed portions (wells) formed in the flexible culture vessel FP are prevented from being unevenly dispersed, and at the same time, the culture fluid which exists at an upper part in the flexible culture vessel FP can be efficiently mixed. In other words, the culture fluid can be gently mixed in the flexible culture vessel FP while the aggregates C′ are kept settled.
The control unit 13 may ad lust the pressing by the pressing member 4 such that the pressure applied to the flexible culture vessel FP remains substantially constant while the mixing member 16 is inserted and moved between the pressing member 4 and the flexible culture vessel FP. In other words, the control unit 13 may adjust the pressing by the pressing member 4 such that the internal pressure of the flexible culture vessel FP does not change before and after the mixing member 16 is inserted and moved between the pressing member 4 and the flexible culture vessel FP.
As a matter of fact, the internal pressure of the flexible culture vessel FP changes by the insertion and movement of the mixing member 16. However, by lifting the pressing member 4 a little by the control unit 13 (moving the pressing member 4 away from the placement surface), for example, the above-described rise in the internal pressure by the mixing member 16 can be offset.
As a consequence, the above-described mixing operation by the mixing member 16 can be performed without giving unnecessary effects to the aggregates C′ in the flexible culture vessel FP.
As the mixing member 16, one having the shape that is rectangular in cross-section and has been chamfered in the round shape at the four corners thereof is used in the present embodiment, but the mixing member 16 is not limited to such a shape.
As depicted in
Further, as depicted in
Furthermore, as depicted in
The mixing member 16 in the present embodiment is disposed so that it extends perpendicularly relative to the inserting and moving direction (Y-direction), but is not limited to such a direction.
As depicted in
Described more specifically, as depicted in
The mixing unit for the culture fluid in the present embodiment described above may be incorporated, for example, in the above-described cell culture apparatus. In addition, the mixing method for the culture fluid in the present embodiment may be incorporated, for example, in the above-described cell culture method.
In addition, in the present embodiment, the mixing member 16 is inserted and moved between the pressing member 4 and the flexible culture vessel FP with the outer surface of the flexible culture vessel FP, the outer surface being in contact with the placement surface, being kept deformed under the pressing by the pressing member 4, but the present invention is not limited to such a mode. Described specifically, the mixing member 16 may be allowed to slide and move on the upper surface of the flexible culture vessel FP with the outer surface, which is on the side of the placement surface, of the flexible culture vessel FP being kept deformed without using the pressing member 4, for example, as in the second embodiment and the fourth embodiment. In other words, the mixing member 16 may be slidingly moved on the upper surface of at least the flexible culture vessel FP with the flexible culture vessel FP being kept deformed at its outer surface on the side of the placement surface by applying an external force.
To the above-described individual embodiments, various modifications are possible within a scope not departing from the spirit of the present invention. A description will hereinafter be made about modifications applicable to the individual embodiments as desired. Those which exhibit the same functions and advantages as the above-described elements in the respective embodiments are identified by like reference symbols, and their description is omitted unless needed.
After a pressing force is applied to the flexible culture vessel FP placed on the placement surface of the stage 2 by the pressing member 4, the control unit 13 then controls the pressure applying devices 5 to perform control so that the pressing member 4 is rocked (swung) in a small range about the X-axis while maintaining the pressing.
According to modification 1, by swinging the pressing member 4 about the X-axis, the culture fluid in the flexible culture vessel FP is mixed, whereby the culture fluid and permeated gas in the flexible culture vessel FP are effectively mixed together.
In the present modification, the description has been made of the example in which the pressing member 4 is swung about the X-axis. However, the pressing member 4 may be swung about the Y-axis, or may be swung about a desired axis other than the X-axis and Y-axis.
As described above, according to the modification 1, even relatively small swings of the pressing member 4 can produce large movements of the culture fluid in the flexible culture vessel FP. The modification 1 is, therefore, considered to be suited when such vigorous mixing (suspension) as swirling the cells C in the flexible culture vessel FP is conducted.
Accordingly, the modification 1 is not only limited to a cell culture apparatus but is also effective as a mixing method and mixing unit for a culture fluid. The mixing method for the culture fluid is characterized by pressing the flexible culture vessel FP, in which cells C and the culture fluid are filled, by the pressing member 4 with the flexible culture vessel FP being kept placed on the placement surface, and swinging the pressing member 4 to perform mixing of the culture fluid with the outer surface, which is in contact with the placement surface, of the flexible culture vessel FP being kept deformed under the pressing by the pressing member 4. On the other hand, the mixing unit for the culture fluid is characterized by including the placement surface that exert a deformation on the outer surface of the flexible culture vessel FP with cells C and the culture fluid filled therein, the pressing member 4 that applies a pressure to the flexible culture vessel. FP placed on the placement surface, and the control unit 13 that performs control to swing the pressing member with the pressure being kept onto the flexible culture vessel FP by the pressing member 4.
As depicted in
As depicted in
According to the modification 2, the boundary between the placement surface 2′″a and each depression 2′″b takes an obtuse angle by the tapered wall 2′″c, so that the flexible culture vessel FP is prevented, for example, from being carelessly damage upon placing the flexible culture vessel FP on, the stage 2′″.
It is to be noted that the present invention shall not be limited to the respective embodiments and respective modifications described above and various combinations and alterations are possible within a scope not departing from the spirit of the present invention.
For example, the placement surface, which exerts a deformation on the outer surface of the flexible culture vessel, has been formed by providing one or more depressions (through-holes or recessed portions) in the placement surface in the above description. Without being limited to the foregoing, a shape having plural tiny projections (short pins or the like) extending upright from a placement surface or the surface of a network-patterned member such as a wire net may be formed as a placement surface, for example.
The present invention can be suitably used, for example, when cells are mass-cultured while forming cell aggregates especially in a cell culture process.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2015-124785 | Jun 2015 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2016/068212 | 6/20/2016 | WO | 00 |
