CELL CULTURE DEVICE

Abstract

A cell culture device is provided, which comprises a cavity and a base layer, wherein the base layer is a type of plastic thin film and has a thickness of 1 μm to 100 μm; a second-moment of inertia lower than 6×10.sup.6 μm.sup.4; and a resultant flexural rigidity of 1×10.sup.−6 Pa.Math.m.sup.4 to 0.02 Pa.Math..sup.4. Accordingly, the base layer can produce an out-of-plane strain, and bending deformation can occur. Therefore, a growth space close to in vivo environment is provided by the base layer for the cells when the cells attach to the base layer, thereby promoting the growth and maturation of the cells and tissues.

Claims

1. A cell culture device, comprising: a cavity including opening and a bottom; and a base layer disposed at the bottom of the cavity and closing the bottom; wherein the base layer is made of a plastic thin film.

2. The cell culture device as claimed in claim 1, wherein a thickness of the base layer is 1 μm to 100 μm, a second-moment of inertia is lower than 6×10.sup.6 μm, and a resultant flexural rigidity is 1×10.sup.−6 to Pa.Math.m.sup.4 to 0.02 Pa.Math.m.sup.4.

3. The cell culture device as claimed in claim 2, wherein the plastic thin-film is at least one selected from the group consisting of polymethyl methacrylate, polypropylene, polystyrene, polyethylene, polyethylene terephthalate, polyvinyl chloride, polydimethylsiloxane, polyurethane, polyacrylamide, and mixtures thereof.

4. The cell culture device as claimed in claim 1, wherein the base layer further includes microgrooves, the microgrooves are arranged parallel or concentrically.

5. The cell culture device as claimed in claim 4, wherein a width of each of the microgrooves is 5 μm to 50 μm, a gap between the adjacent microgrooves is 5 μm to 50 μm.

6. The cell culture device as claimed in claim 4, wherein a depth of each of the microgrooves is 1 μm to 10 μm.

7. The cell culture device as claimed in claim 1, further comprising a hollow spacer disposed under the base layer and contacting with an edge of the base layer.

8. The cell culture device as claimed in claim 1, further comprising a coating layer formed on the base layer, the coating is at least one selected from the group consisting of matrix hydrogel, collagen, fibronectin, laminin, gelatin, and mixtures thereof.

9. A cell culture multi-well plate, comprising: a main body including an accommodating space and a first surface; and a plurality of the cell culture device claimed in claim 1, each of the plurality of cell culture devices is disposed in the accommodating space; wherein the opening of the cavity of each of the plurality of cell culture devices is formed on the first surface.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0018] FIG. 1 is a schematic diagram showing the cell culture device of an embodiment of the present invention;

[0019] FIG. 2 is a sectional view showing the cell culture device of an embodiment of the present invention;

[0020] FIG. 3 is a sectional view showing the cell culture device of another embodiment of the present invention;

[0021] FIG. 4 is a schematic diagram showing the cell culture device of yet another embodiment of the present invention;

[0022] FIG. 5 is a schematic diagram showing the cell culture multi-well plate of an embodiment of the invention;

[0023] FIG. 6 shows the fluorescent images of the cells of Examples 1 to 5 and Comparative example 1;

[0024] FIG. 7 shows the fluorescent images of the cells of Examples 6 to 10 and Comparative example 2;

[0025] FIG. 8 shows the fluorescent images of the cells of Examples 11 to 14;

[0026] FIG. 9 shows the fluorescent images of the cells of Examples 15 to 18;

[0027] FIG. 10 shows measured sarcomere lengths of the cells of Examples 6 to 9 and 15 to 18;

[0028] FIG. 11 shows the cell ellipticity of the cells of Examples 6 to 9 and 15 to 18;

[0029] FIG. 12 shows the total fluorescence intensity of calcium ion wave in cardiomyocytes of Examples 19-20 and Comparative examples 3-4;

[0030] FIG. 13 shows the beating frequency of cardiomyocytes of Examples 19-20 and Comparative examples 3-4.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

Preparation of the Cell Culture Device

[0031] The cell culture device 1000 provided by the present invention is illustrated in FIG. 1. FIG. 1 shows the schematic diagram and FIG. 2 shows the cross-sectional view along the A-A section line in FIG. 1 of the cell culture device 1000 provided by the present invention. The cell culture device 1000 comprises a cavity 1 and a base layer 2.

[0032] The cavity 1 is a hollow cylinder including an opening 11 and a bottom 12 corresponding to the opening 11. The base layer 2 is disposed to the bottom 12 of the cavity 1 and closes the bottom 12. In other embodiments, the shape and size of the cavity 1 are not particularly limited. For example, the shape of the cavity 1 can be square, rectangle, or round, which can be designed according to cell culture requirements.

[0033] The base layer 2 is made of a plastic thin film, the thickness thereof may be 1 μm to 100 μm, a second-moment of inertia may be lower than 6×10.sup.6 μm.sup.4, and a resultant flexural rigidity may be 1×10.sup.−6 Pa.Math.m.sup.4 to 0.02 Pa.Math.m.sup.4. For example, the plastic thin-film can be materials with better biocompatibility such as polymethyl methacrylate (PMMA), polypropylene (PP), polystyrene (PS), polyethylene (PE), polyethylene terephthalate (PET), polyvinyl chloride (PVC), polydimethylsiloxane (PDMS), polyurethane (PU), polyacrylamide (PAM), and mixtures thereof The base layer 2 used in embodiments and comparative embodiments of the present invention was made of polypropylene, polystyrene, polyvinyl chloride, or polydimethylsiloxane.

[0034] In other embodiments illustrated in FIG. 3, the base layer 2 includes microgrooves 21 arranged parallel to each other or concentrically. Those microgrooves 21 were prepared by the hot embossing method. The width of each of the microgrooves is 20 μm; the depth of each of the microgrooves is 4 μm, and the gap between the adjacent microgrooves is 20 μm. The microgrooves 21 can further reduce the second-moment of inertia and the resultant flexural rigidity of the base layer 2 to provide a base layer 2 with higher flexibility and bending ability, and can also induce myocytes to align into long and narrow cells.

[0035] Furthermore, as shown in FIG. 2 and FIG. 3, the cell culture device 1000 further comprises a coating layer 3. The coating layer 3 is an extracellular matrix to promote cell attachment on the base layer 2. In other embodiments, the coating layer 3 may be other materials that improve cell attachment, such as matrix hydrogel, collagen, fibronectin, laminin, gelatin, and mixtures thereof, which is not particularly limited.

[0036] The hollow spacer 4 is disposed beneath the base layer 2 and contacts with the edges of the base layer 2 as illustrated in FIG. 4. The hollow spacer 4 is mainly used to prevent the base layer 2 from contacting the underlying working surface or other elements during the process of culturing the cells 5 thereon so that the base layer 2 can generate the out-of-plane strain when the cells 5 are cultured thereon. On the other hand, the hollow spacer 4 also provides an edge that the users can rely on when suctioning and adding reagents, to prevent the user from puncturing the base layer 2.

[0037] In other embodiments, a cell culture multi-well plate 2000 illustrated in FIG. 5 is formed with a plurality of the cell culture device 1000, wherein the number and shape of the cell culture device 1000 may be designed according to cell culture requirements without limitation.

Cardiomyocyte Culture

[0038] The cells used in the evaluations of the examples and comparative examples of the present invention are cardiomyocytes induced and differentiated from human-induced pluripotent stem cells (hiPSC). The thawed cardiomyocytes were cultured on the 35th day, the cells with different cell densities (10,000 cells/well and 40,000 cells/well) were seeded respectively into cell culture devices with different base layer thicknesses, materials, or micro-grooved structures, and the cells were fixed on the 40th day of culture. Staining and quantitative analysis were then performed.

Quantitative Analysis of Cardiomyocytes

[0039] The fixed cardiomyocytes were fluorescently stained, wherein the nucleus was stained with Hoechst 33342 (Thermofisher ab 228551);

[0040] a-actin was stained with anti-a-actin antibody mouse monoclonal IgG1 AT6/172 (Millipore MAB1682) used as the primary antibody stain, and FTTC Conjugated Goat Anti-Mouse IgG antibody (H+L) used as the secondary antibody stain; while F-actin was stained with Alexa Flour Phalloidim.

[0041] An inverted fluorescent microscope (IX71, Olympus) was used with different fluorescence filters to excite the nucleus, α-actin, and F-actin stained with dyes in cardiomyocytes.

[0042] The captured α-actin fluorescence images were loaded in the built-in software of the inverted fluorescence microscope. Then, the built-in Line profile was used to calculate the length of the sarcomere lengths of the cells.

[0043] Furthermore, the software Image J was used to find the boundary of a single cell, and the fluorescence photos taken in advance were loaded. The Threshold function was used to find the cell membrane boundary of the cardiomyocytes, and the cell boundary was displayed using the function of Edges Finder to calculate the area of the cell (A).

[0044] In addition, the major axis length and the minor axis length of a single cell were measured by the software Image J, and the following formula was introduced to obtain the ellipticity.

Ellipticity=(major axis length−minor axis length)/major axis length

Data Analysis

[0045] In the present invention, each experiment was repeated three times, and 9 cells were be randomly selected for quantitative analysis in each experiment. The data were analyzed by ANOVA using excel, wherein * means P value≤0.05; ** means P value≤0.01; *** means P value≤0.001, and indicate that there is a significant difference between the two groups of data, and a P value>0.05 indicates that there is no significant difference between the two groups of data.

Evaluation of the Effect of Different Thicknesses of the Base Layer on Cardiomyocytes

[0046] First, for the evaluation of the effect of base layers with different thicknesses on high-density cultured cardiomyocytes, please refer to the base layer materials and thicknesses of Examples 1-5 and Comparative Example 1 shown in Table 1. The sarcomere length was used as the evaluation criterion, and the longer the sarcomere length, the more mature the cardiomyocytes.

TABLE-US-00001 TABLE 1 Thickness Cell density Sarcomere Material (μm) (cells/well) length (μm) Example 1 PP 75 40000 1.75 Example 2 PP 30 40000 1.79 Example 3 PP 18 40000 1.79 Example 4 PS 10 40000 1.79 Example 5 PVC 5 40000 1.91 Comparative PDMS 1000 40000 1.74 example 1

[0047] Please refer to the fluorescent images of the cells shown in FIG. 6 (scale bar=10 μm), the cell morphology showed that the cardiomyocytes cultured on the flat base layer were mostly round and loosely arranged. Refer to the sarcomere lengths recorded in Table 1, it should be noted that the sarcomere lengths of the cardiomyocytes cultured at high density on the base layer with a thickness of 5 μm to 75 μm were significantly higher than those of the cardiomyocytes in Comparative Example 1. Cardiomyocytes cultured on a base layer with a thickness of 5 μm had the longest sarcomere length. It confirmed that reducing the thickness of the base layer can reduce the flexural rigidity of the film, making the device more suitable for cell culture.

[0048] Next, an evaluation of the effects of base layers with different thicknesses on cardiomyocytes cultured at low density was made. The materials and thicknesses of the base layers of Examples 6-10 and Comparative example 2 are shown in Table 2, the sarcomere length, cell area, and cell ellipticity were evaluated and are also shown in Table 2, wherein the closer the cell ellipticity value was to 1, the more slender the cell shape was, and the closer to 0, the more rounded the cell shape was.

TABLE-US-00002 TABLE 2 Sarcomere Thickness Cell density length Cell Material (μm) (cells/well) (μm) ellipticity Example 6 PP 75 10000 1.64 0.58 Example 7 PP 30 10000 1.67 0.66 Example 8 PP 18 10000 1.67 0.72 Example 9 PS 10 10000 1.67 0.72 Example 10 PVC 5 10000 1.67 0.72 Comparative PDMS 10000 1.68 0.78 example 2

[0049] FIG. 7 shows the fluorescent images of the cells of Examples 6 to 10 and Comparative example 2 (scale bar=20 μm). After analyzing the fluorescence images, the sarcomere length of the cardiomyocytes was obtained and shown in Table 2. According to the results shown in Table 2, the sarcomere length increased from 1.56 μm to 1.67 μm when the thickness of cardiomyocytes decreased from 75 μm to 5 μm. It is confirmed that reducing the thickness of the base layer for reducing the flexural rigidity of the film can promote the maturation of cardiomyocytes. Next, please refer to the cell ellipticity recorded in Table 2. It can be seen that under the low-density culture of cardiomyocytes, the cardiomyocytes on the base layer of Comparative Example 2 showed an oval shape, and when the thickness of the base layer gradually decreased, the cell ellipticity of cardiomyocytes gradually increased, which means that when the thickness of the base layer was smaller, the cardiomyocytes culture thereon were more mature.

Evaluation of the Effect of the Base Layer with Microgrooves on Cardiomyocytes

[0050] The base layer of the cell culture device provided by the present invention may further include elongated microgrooves, and the microgrooves may also be arranged in parallel or concentrically. In this evaluation, the width and spacing of the microgrooves were 20 μm, the depth was 4 μm, and the microgrooves were formed on the base layer with different thicknesses as described above. The evaluation of high-density cultured cardiomyocytes was performed, please refer to Examples 11-14 shown in Table 3, and the sarcomere length of cardiomyocytes was used as the judgment standard.

TABLE-US-00003 TABLE 3 Thickness Cell density Sarcomere Material (μm) (cells/well) length (μm) Example 11 PP 75 40000 1.86 Example 12 PP 30 40000 1.90 Example 13 PP 18 40000 1.81 Example 14 PS 10 40000 1.91

[0051] Please refer to the fluorescence images shown in FIG. 8 (scale bar=10 μm), it can be seen that cardiomyocytes grow along the extension direction of the microgrooves and produce relatively complete bonds. After comparing the sarcomere lengths of cells in Examples 1 to 5 without microgrooves, it can be found that in the base layer of 75 μm, the sarcomere length of cardiomyocytes cultured on the base layer with microgrooves increased from 1.75 μm to 1.86 μm, which was about 6.3% increase; in the base layer of 30 μm, the sarcomere length of cardiomyocytes cultured on the base layer with microgrooves increased from 1.79 μm to 1.90 μm, which was about 6.2% increase; and in the base layer of 10 μm, the sarcomere length of cardiomyocytes cultured on base layer with microgrooves increased from 1.79 μm to 1.91 μm, which was about 6.7% increase. The main function of the microgrooves was to reduce the second moment of inertia and flexural rigidity of the base layer to a lower value by changing the cross-sectional shape of the base layer to provide a base layer with higher flexibility and bending ability. The microgrooves also guided the myocytes to be arranged into a long and narrow structure. The addition of the microgroove structure had a significant effect on the sarcomere length of the cardiomyocytes for the base layer of different thicknesses, which can promote the maturity of the cardiomyocytes and improve the compliance of the base layer.

[0052] Next, the effect of the base layer including microgrooves with different thicknesses on the cardiomyocytes cultured at low density was evaluated. Please refer to Examples 15-18 shown in Table 4, the sarcomere length, the cell area, and the cell ellipticity were used as judgment standards.

TABLE-US-00004 TABLE 4 Thickness Cell density Sarcomere Cell Cell Material (μm) (cells/well) length (μm) area ellipticity Example 15 PP 75 10000 1.68 2751.3 0.81 Example 16 PP 30 10000 1.67 2561.4 0.85 Example 17 PP 18 10000 1.69 2691.1 0.87 Example 18 PS 10 10000 1.70 2450.7 0.86

[0053] Please refer to the fluorescence images of Examples 15 to 18 shown in FIG. 9 (scale bar=20 μm), and the sarcomere length of the cells of Examples 6 to 9 (without microgrooves) and 15 to 18 (with microgrooves) shown in FIG. 10. It can be found that in the base layer of 75 μm, the sarcomere length of the cardiomyocytes cultured after adding microgrooves increased from 1.64 μm to 1.68 μm, which was 2.4% increase; in the base layer of 30 μm, the sarcomere length of the cardiomyocytes cultured after adding microgrooves remained at 1.67 μm; in the base layer of 18 μm, the sarcomere length of the cardiomyocytes cultured after adding microgrooves increased from 1.67 μm to 1.69 μm, which was 1.2% increase; and in the base layer of 10 μm, the sarcomere length of the cardiomyocytes cultured after adding microgrooves increased from 1.67 μm to 1.70 μm, which was 1.8% increase. Accordingly, the base layer of different thicknesses can have a significant effect on the sarcomere length of cardiomyocytes whether the microgrooves were included or not. Next, please refer to the cell ellipticity of Examples 6 to 9 (without microgrooves) and 15 to 18 (with microgrooves) shown in FIG. 11; the comparison results show that the microgrooves have a significant impact on the cell ellipticity. Comparing to the flat base layer (without microgrooves), the cardiomyocytes cultured on base layers with microgrooves were more mature.

Evaluation of the Effect of Different Thicknesses of the Base Layer on Cardiomyocyte Maturation

[0054] To observe the maturation of cardiomyocytes cultured on base layers of different thicknesses, the performance of calcium ion waves of human-induced pluripotent stem cell differentiated cardiomyocytes after 15 days of culture in different base layers was investigated in this evaluation. The base layer of Example 19 was made of polyvinyl chloride (PVC) with a thickness of 10 μm, the base layer of Example 20 was made of PVC with a thickness of 5 μm, and in Comparative Examples 3 and 4, the base layers were respectively made of PMMA and PDMS with a thickness of 1 mm.

[0055] The results of the evaluations were shown in FIG. 12 and FIG. 13. FIG. 12 was the total fluorescence intensity of the cardiac calcium ion wave, and FIG. 13 was the comparison result of the beating frequency of the cardiac muscle. According to the results, there was no significant difference in the total fluorescence intensity of calcium ion waves between Examples 19 to 20 and Comparative examples 3 to 4. In contrast, the beating frequency of cardiomyocytes increased with the decrease of the thickness of the base layer. This experiment proved that the use of plastic thin-film as the base layer of the cell culture device can compensate for the tissue stiffness compared to the in vivo environments and provide a better culture environment and promotes the development of cells into mature cells and muscle tissue.

[0056] Based on the above evaluation results, when cardiomyocytes were cultured in a high-density environment, the cells interacted with each other. Mature cardiomyocytes are connected to form myocardial tissue and promote the increase in cell sarcomere length. As the thickness of the base layer decreases, especially when the thickness of the basal layer was 5 μm, the phenomenon of increasing the cell sarcomere length was significant. Therefore, it is verified that when the thickness of the base layer is reduced, the bending deformation of the base layer will increase when the cardiomyocytes contract on the base layer. The better cell culture conditions can be achieved by solving the problem of high stiffness of the base layer. When the microgrooves are introduced to the base layer, the bending ability and flexibility of the base layer can be further improved. At the same time, the cardiomyocytes tend to be connected and arranged with each other, and the cell sarcomere length thereof can be significantly increased, so that the maturity of the cardiomyocytes can be greatly improved. When cardiomyocytes were grown in a low-density environment, the change in cell sarcomere length of cardiomyocytes was similar to that of cardiomyocytes cultured in a high-density condition. In terms of cell area, it can be seen that when the thickness of the base layer decreased, the morphology of cardiomyocytes became slender as the mature cells, and the homogeneity was also improved. In terms of cell ellipticity, it can be seen that as the thickness of the base layer decreased, the cell ellipticity gradually increased. When microgrooves were added to the base layer, the maturity of cardiomyocytes was improved.

[0057] In summary, the cell culture device provided by the present invention is flexible and can be designed with microgrooves, which is beneficial for improving the maturity of myocytes. The high flexibility achieved by reducing the thickness of the base layer can imitate the in vivo growth conditions of myocytes, so that the myocytes cultured in vitro have a similar growth environment, and the deformation amount and contraction distance can be increased during contraction.

[0058] The cell culture device provided by the present invention is not limited for culturing cardiomyocytes, skeletal myocytes, smooth myocytes, and various adherent cells may be cultured thereon.