Cell culture incubating apparatus and method using the same

Abstract

A cell incubating apparatus and a method of culturing a cell in vitro are disclosed, which relates to a medical cell proliferation, pharmaceutical screening and automatic cell analysis in tissue engineering technology. The apparatus establishes an imitating three-dimensional transportation microenvironment by assembling a top plate, a bottom plate and at least one culture plate apparatus for incubating a cell. The apparatus is not only for incubating the tissue specific cell with biological function but also for lowering the cost of culturing personal medical cells.

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention

The invention is related to a cell incubating apparatus and the method of culturing a cell in vitro, and especially, relates to a medical cell proliferation, pharmaceutical screening and automatic cell analysis in tissue engineering technology.

2. Description of Related Art

In the field of tissue engineering, cell transplantation will play an important role in the future. Currently, the cell expansion apparatuses, which comprise not only for traditional laboratory cell incubating techniques but also for traditional bioreactors, have limitation for incubating a medical cell source. The shortcoming of the traditional laboratory cell incubating techniques mentioned above is the lack of a mass transporting system and difficult to display the real physiological activities ongoing inside the cell body. The bioreactor is only suitable in protein drug production as in, for example, the production volume of the stromal cells and fibroblasts with better tolerance for the above shortcoming. The bioreactor is excessively large and difficult to operate, has large fluidic shear force, lacks micro-environments similar to the physiological environment, and is impossible to incubate some tissue specific cells so far, for example, hepatocytes. Besides, using these bioreactor to produce personal cells is expensive, therefore, it is difficult industrializing cell production for personal cell therapy.

Massachusettes Institute of Technology and Massachusetts General Hospital in the United States disclosed a system containing micromaxtrix, an injection unit and sensors in WO9947922. The system is mainly used in pharmaceutical screening and analysis. However, even through the system illustrated above can maintain the cell function in vitro, the cells in the system forms a cell mass which is hard to isolate and expand. In the patent pended by University of California at San Diego, U.S. Pat. No. 20020072116, disclosed a nanoporous silicon bioreactor which is used for pharmaceutical screening such as analysis for the biological activity, metabolism, toxicity, mutagenicity or carcinogenicity of compounds. However, such a bioreactor is only for maintaining the function in vitro and not fit for cell proliferation.

Therefore, it is desirable to provide an improved method to mitigate the aforementioned problems.

SUMMARY OF THE INVENTION

The cell incubating apparatus of the present invention relates to a cell culture device that can establish an imitating three-dimensional mass transportation microenvironment, which assists the formation of cell cytokine gradient and the heterocellular reaction. The cell incubating apparatus is not only for incubating the tissue specific cells with biological function but also to lower the cost of cell production for personal medical treatment.

Another purpose of the present invention relates to a method of culturing cell in vitro. This method will establish an imitating three-dimensional transportation microenvironment, which assists to the formation of cell endocrine gradient and the reaction between different types of cells. The cell incubating apparatus of the present invention is not only for incubating the tissue-specific cell with a biological function but also for lowering the cost of culturing cells for personal medication.

To achieve the purpose above, the cell incubating apparatus of the present invention, which cooperates with a fluid, comprises: a top plate having an input hole; a culture plate having a plurality of incubating units, a receiving part, an output hole, and a fluid tract; and a bottom plate for collecting the fluid form the top plate and the culture plate. Among them, the incubating units and the fluid tract are located on at least one surface of the culture plate. The fluid tract connects the multiple culture units, and the receiving part. The receiving part overlaps the input hole in the top plate to receive the fluid from the input hole. The output hole is located in the incubating unit for outputting the fluid. Moreover, the culture plate is sandwiched between the top plate and the bottom plate as assembled, the fluid flows into the receiving part on the surface of the culture plate from the input hole, passes along the flow path then flows into the culture units, and arrives in the bottom plate from the output hole.

The method of the present invention comprises following steps: (A) providing an apparatus comprising a top plate having an input hole; a culture plate having a plurality of incubating units, a receiving part, an output hole, and a fluid tract; and a bottom plate for collecting the fluid form the top plate and the culture plate as illustrated above; (B) seeding stromal cells to cover the culture unit; and (C) filling in a fluid into the input hole on the top late, and the fluid flows to the bottom plate by passing the receiving part, the culture unit, flowing path, and the output hole.

Other objects, advantages, and novel features of the invention will become more apparent from the following detailed description when taken in conjunction with the accompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an exploded perspective view of the present invention relating to an incubating cell apparatus

FIG. 2 is a perspective view of an assembly of the present invention relating to an incubating cell apparatus

FIG. 3A and FIG. 3B are the morphology of HepG2 cells incubated in fluidic condition.

FIG. 3C and FIG. 3D are the morphology of HepG2 cells incubated in a static condition.

FIG. 4 is transimission electron microscope image of HepG2 cells cultured in fluidic setting. Microvilli formed have been observed.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

The present invention relates to a cell incubating apparatus preferably comprising a surface of a bottom plate, which is formed with a plurality of micro paths overlapping the output holes for collecting or converging the fluid. More preferably, the bottom plate surface is provided with a collecting trough connected to the micro paths for collecting the fluid. The invention of the incubating apparatus comprises, even more preferably, a transporting tract that connects to the collecting trough and input hole for refluxing the fluid back to the input hole, or the relative location of collecting through the culture plate and the top plate, preferably formed with one spill hole and one over through hole, whereby the collecting trough extends through the through hole, the spill hole and the transporting tract and then connects to the input hole. The present invention discloses an incubating apparatus, wherein the top plate preferably comprises a plurality of apertures overlapping the culture units for testing the interaction between different cells, more preferably, a thin biologically compatible membrane is provided between the top plate and the bottom plate as an interface for interaction between cells. The invention can optionally include at least one micro flowing path. The micro flowing path is formed with a micro path system, which is similar to capillaries. Depending on the requirements, the culture unit also can be seeded and covered by the stromal cell for facilitating the attachment of the cells. The material of the top plate, culture plate and bottom plate of the incubating apparatus of the present invention can be made of any traditional material with machinability. Preferably, the material of the top plate, culture plate and bottom plate are transparent material, more preferably, the material of the top plate, culture plate and bottom plate are acrylic, polycarbonate (PC) or polydimethylsiloxane (PDMS). The invention also relates to a method in incubating a cell in vitro, which comprises, preferably, one transporting tract to connect a collecting hole and an input hole for refluxing the fluid back to input hole. The method of incubating a cell in vitro, more preferably comprises a plurality of apertures overlapping the culture units on the top plate in order to analyze the interaction in different cells. More preferably, the apparatus used in the method of the present invention is provided with a biological membrane located between the apertures and the culture units for providing an interface of cell interaction. The invention relates to the method of incubating a cell in vitro, which even more preferably comprises forming at least one micro path on the culture unit to imitate a micro path system similar to blood capillary. e. The materials of the top plate, culture plate and bottom plate included in the present method are preferably made of transparent material, and more preferably are made of acrylic polymers, PC or PDMS. The method of the present invention comprises preferably a step of using one illuminant on the incubating apparatus in order to observe the cellular activity.

With reference to FIG. 1, the invention of the incubating cell apparatus comprises a top plate 10, a culture plate 20 and a bottom plate 30. The bottom plate 30 is sandwiched between the top plate 10 and the bottom plate 30. The top plate 10, culture plate 20 and bottom plate 30 are respectively formed with screw holes 15, 25, and 35 in order to fasten them together using securing elements such as screws. The top plate 10 is provided with an input hole 11, a plurality of apertures 12 and a spill hole 13. The surface of culture plate 20 is formed with a plurality of culture units 21, a flow path 22, which is connected to each culture unit 21 and a through hole 23. The flow path 22 is provided with a receiving part 221 to receive the fluid from an incubating apparatus and the fluid is injected into the receiving part 221 via the input hole 11. The culture units 21 each comprise a circular hole 211 for separating the flowing. The circular hole 211 connects to the culture well 213 with a strike hole 212 and the culture well 213 is provided with an output hole 214. After the fluid is poured into the culture plate 20, the fluid passes through the output hole 214 and then directly flows down to the bottom plate 30. The culture well 213 on culture plate 20 overlaps the aperture 12 on the top plate 10. Respective different cells in aperture 12 and culture well 213 are allowed to culture for testing heterocellular interaction. The culture plate also can be seeded or covered with a biological membrane between the culture well 213 and the aperture 12 to be an interface of cell interaction. The surface of bottom plate 30 is formed with a plurality of micro paths overlapping the output hole 214 and a collecting trough 32. The output hole 214 connects with the micro path 31. The micro path 31 can converge the fluid from output hole 214 and collect in the collecting trough 32. The location of the collecting trough 32 aligns with the spill hole 13 on top plate 10 and the through hole 23 on the culture plate 20. By using one side of the micro path 31 connecting to the input hole 11 and the other side of that connecting to the transporting tract of the collecting trough (not shown in the figure), which extends through the spill hole 13 and the through hole 23, the fluid collecting from the collecting trough 32 can be refluxed into the input hole 11.

When performing the cell culture, the cells are loaded first. The cell incubating apparatus of the present invention is provided with several possible methods for cell loading, for example, the extracellular matrix is coated on the culture well 213 first and the cells are seeded. Cells are allowed to attach after 24 hours, then top plate 10, culture plate 20 and bottom plate 30 are assembled and secured with a screw 40 to form a cell incubating apparatus as shown in FIG. 2. After the apparatus has been assembled, the culture solution is filled from the input hole 11 into the top plate. The culture solution flows along the flow path 22 and then respectively flows into the micro path, which is similar to capillaries, and the culture well 213. After the culture plate 20 has been filled with the culture solution, the culture solution vertically flows down to the micro path 31 on the bottom plate 30 and then converges into the collecting trough 32 to form micro fluids that is similar to capillaries, in order to proceed the mass transfer, or build up the cell incubating apparatus first after coated with the extracellular matrix on culture well 213, after which the filling procedure is begun. The cells circulate in the flowing path and obtain a higher cell seeding density. Then the flowing speed is reduced to zero, and wait for 4-6 hours, and then the filling procedure is carried out at low speed. After cells loading into the present invention of cell incubating apparatus as mentioned above, the filling procedure is started at different speeds and different compositions of each culture plate. After completion of the decided time period, for example, after 1, 2, 5 or 7 days, it can be observed by a microscope if there is any morphological changes occurred in cell structure. As shown in FIGS. 3A˜3D, HepG2 cells were cultured respectively in the present invention and some prior art of cell incubating apparatus, the result shows that to compare to culture cell in the prior art of stationary culture technique, which forms some circular structure in FIG. 3C and FIG. 3D. The cell incubating apparatus of the present invention displays an island shape of cell structure in the present cell incubating invention and is also very similar to the physical structure. FIG. 4 is a transmission electron microscopic graph of cells after undergoing the flowing incubating method, wherein microvilli is located in the left bottom circle, and a tight junction is located in the right top circle. It is shown that the cultured cell structure is provided with microvilli and tight junction, which are the specialized structure taken from hepatic tissue. The result shows that the cell-cultured environment supplied by the present invention is provided with the ability of imitating real physical function.

To perform the analysis procedures, for example, the growth factors in the system keep released when cells are under stimulations, the cell incubating apparatus of the present invention will transport the fluid from the collecting well 32, pass through the through hole 23, spill hole 13 and transport tract to the transporting hole 11. Then the fluid will circulate in the path of the present invention mentioned above. In the meantime, for the preferable example, the material of top plate 10, culture plate 20 and bottom plate 30 are transparent PC. The cell incubating apparatus of the present invention can be used for testing cellular activity by photon detection system as illustrated by prior arts. On the other hand, the present invention is also provided with a plurality of culture plates between the top plate and the bottom plate; each culture plate can incubate the same or different cells. If the cells are the same, the cell incubating apparatus of the present invention can be expanded for cell proliferation. If the cells are different, the cell incubating apparatus of the present invention can be used for the observation of cell-cell interaction between the cells.

In reference to tissue engineering, the cell related products need highly personalized; the cell incubating apparatus of the present invention is also needed to combine with biomedica and scale-up technologies beneficial for marketing purpose. The present invention combines the cell physiology knowledge with industrialization purpose, and develops the new generation of bio-mimetic cells incubating system, which is provided with high specification, high density and also mimics the mass transportation system within cells, in order to apply in cell proliferation for medical, pharmaceutical screening and automatic cell analysis. The present invention relates to a novel technique in tissue engineering, which is applied with bio-mimetic techniques in a tissue-specific cell-simulating physiological system. The present invention is in an advantage of the 3D physical simulating system that can display the real cellular activity in vivo and also help to form cell cytokine/chemokine gradient and hetrocellular interactions, in order to culture the tissue-specific cells for a delicate microenvironment. The cell incubating apparatus of the present invention can also reduce the production cost, provide a manufacture process with an industrialized capability, and in addition can be designed for multiple productions, for disposable productions. The apparatus will proceed to manufacture the reaction system with low production cost and high additional value for future personal medical application.

Although the present invention has been explained in relation to its preferred embodiment, it is to be understood that many other possible modifications and variations can be made without departing from the spirit and scope of the invention as hereinafter claimed.

Claims

1. A cell incubating apparatus, which used with a fluid, comprising: a top plate having an input hole; a culture plate having a plurality of incubating units, a receiving part, an output hole, and a fluid tract; wherein the incubating units and the fluid tract are located on at least one surface of the culture plate, the fluid tract connects to the multiple culture units, the receiving part overlapping the input hole in the top plate to receive the fluid from the input hole, the output hole located in the incubating unit for outputting the fluid; and a bottom plate for collecting the fluid form the top plate and the culture plate; wherein the culture plate is sandwiched between the top plate and the bottom plate as assembled, the fluid flows into the receiving part on the surface of the culture plate from the input hole, passes along the flow path then flows into the culture units, and arrives in the bottom plate from the output hole.

2. The cell incubating apparatus as claimed in claim 1, wherein the surface of bottom plate is provided with a plurality of micro tracts overlapping the output hole in order to collect or to converge the fluid.

3. The cell incubating apparatus as claimed in claim 2, wherein the surface of bottom plate is provided with a collecting trough connected to a micro flow path for collecting the fluid.

4. The cell incubating apparatus as claimed in claim 3, further comprising a transport tract, which is connected to a collecting trough and the input hole in order to reflux the fluid to the input hole.

5. The cell incubating apparatus as claimed in claim 4, wherein a spill hole and a through hole is formed or provided on the top plate and the bottom plate respectively, and the locations of the spill hole and the through hole are arranged to let the input hole connect the bottom plate through the spill hole, the through hole, and the transporting tract.

6. The cell incubating apparatus as claimed in claim 1, wherein the top plate further comprises a plurality of apertures overlapping the culture unit on the top plate in order to analyze interaction in different cells.

7. The cell incubating apparatus as claimed in claim 6, further comprising a biological compatible membrane, wherein the thin biological compatible membrane is located between the top plate and the culture units.

8. The cell incubating apparatus as claimed in claim 1, further comprising at least one micro path for forming a micro path system, wherein the micro path is located on the culture unit.

9. The cell incubating apparatus as claimed in claim 1, wherein the culture unit is covered with extracellular matrix to facilitate the attachment of the cells.

10. The incubating apparatus as claimed in claim 1, wherein the top plate, the culture plate and the bottom plate are transparent plates.

11. The incubating apparatus as claimed in claim 1, wherein the top plate, the culture plate and the bottom plate are made of acrylic, polycarbonate (PC) or polydimethylsiloxane (PDMS).

12. A method of incubating a cell in vitro, comprising following steps: (A) providing a cell incubating apparatus which comprises: a top plate having an input hole; a culture plate having a plurality of incubating units, a receiving part, an output hole, and a fluid tract; wherein the incubating units and the fluid tract are located on at least one surface of the culture plate, the fluid tract connects to the multiple culture units, the receiving part overlapping the input hole in the top plate to receive the fluid from the input hole, the output hole located in the incubating unit for outputting the fluid; and a bottom plate for collecting the fluid form the top plate and the culture plate; wherein the culture plate is sandwiched between the top plate and the bottom plate as assembled, the fluid flows into the receiving part on the surface of the culture plate from the input hole, passes along the flow path then flows into the culture units, and arrives in the bottom plate from the output hole; (B) coating extracellular matrix to cover the culture unit; and (C) filling in a fluid into the input hole on the top late, and the fluid flows to the bottom plate by passing the receiving part, the culture unit, flowing path, and the output hole.

13. A cell incubating method as claimed in claim 12, wherein the bottom plate is provided with a collecting trough in order to collect the fluid.

14. A cell incubating method as claimed in claim 12, further comprising a transporting tract, which is connected to the collecting trough and the input hole for refluxing the fluid to the input hole.

15. A cell incubating method as claimed in claim 12, further comprising a plurality of apertures overlapping with the locations of culture unit on the top plate in order to analyze the interaction between different cells.

16. A cell incubating method as claimed in claim 15, further comprising a biological compatible membrane which is located between the aperture and the culture unit in order to provide an interface for cell interactions.

17. A cell incubating method as claimed in claim 12, further comprising at least one micro flow path on the culture unit

18. A cell incubating method as claimed in claim 12, wherein the material of the top plate, culture plate and bottom plate are transparent plates.

19. A cell incubating method as claimed in claim 18, further comprising an photon detection system for the cell incubating apparatus in order to scan the activity of the cells.