Microfluid device and three-dimensional microculture method for cell
The invention provides a microfluidic device comprising at least one cell culture chamber, the at least one cell culture chamber being connected to at least two openings, the device being configured to supply at least one physiologically active substance from at least one of the openings to the at least one cell culture chamber in such a manner as to form a concentration gradient or concentration gradients in the at least one chamber when cells and a hydrogel are introduced into the at least one cell culture chamber to culture the cells in a 3D-gel medium.
1. A method of a 3D cell microculture using a microfluidic device having one or more cell culture chambers including one or more openings and one or more tanks connected to the one or more cell culture chambers through the one or more openings, comprising:
introducing a hydrogel into the one or more cell culture chambers, the hydrogel forming a three-dimensional gel having a certain degree of solidity for a highly biocompatible environment;
introducing predetermined cells to be cultured in a uniformly distributed manner in the one or more cell culture chambers; and
supplying at least one physiologically active substance from the one or more tanks to the one or more cell culture chambers through the one or more openings in such a manner as to form a concentration gradient or concentration gradients in the one or more culture chambers.
2. The method of a 3D cell microculture using a microfluidic device according to claim 1 , further comprising forming a three-dimensional gel (3D-gel) cell support carrier from the hydrogel, wherein the concentration gradient or the concentration gradients of the physiologically active substance are formed by the 3D-gel cell support carrier due to diffusion over the 3D-gel cell support carrier.
3. The method of a 3D cell microculture using a microfluidic device according to claim 1 , wherein the hydrogel is fluidized prior to introducing into the one or more cell culture chambers.
4. The method of a 3D cell microculture using a microfluidic device according to claim 1 , wherein the hydrogel and the predetermined cells are introduced substantially at the same time into the one or more cell culture chambers.
5. The method of a 3D cell microculture using a microfluidic device according to claim 1 , further comprising, adjusting the solidity of the three-dimensional gel.
6. The method of a 3D cell microculture using a microfluidic device according to claim 1 , wherein the hydrogel is a phase transition hydrogel.
7. The method of a 3D cell microculture using a microfluidic device according to claim 6 , wherein the phase transition hydrogel includes any combination of chitosan gel, collagen gel, gelatin gel, peptide gel, fibrin gel, starch, pectin, hyaluronic acid, alginic acid, fibronectin, vitronectin, laminin, alginate, and fibroin.
8. The method of a 3D cell microculture using a microfluidic device according to claim 6 , wherein the phase transition hydrogel is a temperature-sensitive phase transition hydrogel and is solidified into the three-dimensional gel based upon a temperature change.
9. The method of a 3D cell microculture using a microfluidic device according to claim 1 , wherein a mixture of the predetermined cells and the hydrogel is introduced into the one or more cell culture chambers.
10. The method of a 3D cell microculture using a microfluidic device according to claim 9 , further comprising, adjusting the solidity of the three-dimensional gel.
11. The method of a 3D cell microculture using a microfluidic device according to claim 1 , wherein the predetermined cells include pluripotent stem cells including human ES and iPS cells.
12. The method of a 3D cell microculture using a microfluidic device according to claim 1 , wherein a growth factor is supplied at a predetermined concentration from the one or more tanks into the one or more cell culture chambers.
13. The method of a 3D cell microculture using a microfluidic device according to claim 1 , further comprising,
deforming the three-dimensional gel into the hydrogel; and
harvesting the cells from the one or more cell culture chambers.
14. The method of a 3D cell microculture using a microfluidic device according to claim 13 , wherein the three-dimensional gel is deformed by adjusting a temperature in the one or more cell culture chambers.
15. The method of a 3D cell microculture using a microfluidic device according to claim 13 , wherein the three-dimensional gel is deformed by decreasing a concentration of the gel.
16. The method of a 3D cell microculture using a microfluidic device according to claim 13 , wherein the three-dimensional gel is deformed by introducing calcium ions.
17. The method of a 3D cell microculture using a microfluidic device according to claim 1 , wherein a plurality of the physiologically active substances is supplied to same one of the culture chambers through a plurality of the openings in such a manner as to form a plurality of the concentration gradients of the physiologically active substances over the three-dimensional gel due to diffusion.
18. The method of a 3D cell microculture using a microfluidic device according to claim 1 , wherein the concentration gradients are in substantially the same direction over the three-dimensional gel.
19. The method of a 3D cell microculture using a microfluidic device according to claim 1 , wherein the concentration gradients are in substantially different directions over the three-dimensional gel.
20. The method of a 3D cell microculture using a microfluidic device according to claim 1 , wherein each of the concentration gradients depends upon the solidity of the three-dimensional gel.
21. The method of a 3D cell microculture using a microfluidic device according to claim 1 , wherein each of the concentration gradients depends upon the molecular weight of the physiologically active substance.
22. The method of a 3D cell microculture using a microfluidic device according to claim 1 , wherein each of the concentration gradients depends upon a combination of the solidity of the three-dimensional gel and the molecular weight of the physiologically active substance.
23. A microfluidic device for cell culture, comprising:
at least one cell culture chamber in a predetermined width, length and depth having a first opening located at one end and a second opening located at the other end along the length, the cell culture chamber containing predetermined cells to be cultured;
at least one first source connected to the cell culture chamber for supplying at least one of predetermined materials to the cell culture chamber through the first opening; and
at least one second source connected to the cell culture chamber for supplying at least one of the predetermined materials to the cell culture chamber through the second opening,
wherein the first opening is unequal to the second opening in size.
24. The microfluidic device for cell culture according to claim 23 , wherein the first source is larger than the second source in volume.
25. The microfluidic device for cell culture according to claim 23 , wherein the first opening is an inlet for supplying the one of predetermined materials to the cell culture chamber while the second opening is an outlet for removing the one of predetermined materials from the cell culture chamber.
26. The microfluidic device for cell culture according to claim 23 , wherein the first source is a first tank that is directly connected to the cell culture chamber through the first opening.
27. The microfluidic device for cell culture according to claim 26 , wherein the second source is a second tank that is connected to the cell culture chamber through the second opening.
28. The microfluidic device for cell culture according to claim 23 , wherein the second source has a plurality of sources each of which is connected to a respective one of channels that are connected to the cell culture chamber through the second opening.
29. The microfluidic device for cell culture according to claim 23 , wherein the first opening is approximately equal to the width of the cell culture chamber.
30. The microfluidic device for cell culture according to claim 23 , wherein the first opening is less than the width of the cell culture chamber.
31. The microfluidic device for cell culture according to claim 23 , wherein the second opening is approximately equal to the width of the cell culture chamber.
32. The microfluidic device for cell culture according to claim 23 , wherein the second opening is less than the width of the cell culture chamber.
33. The microfluidic device for cell culture according to claim 23 , wherein the cell culture chamber has a volume of from about 0.5 μL to about 10 μL.
34. A microfluidic device for cell culture, comprising:
at least one cell culture chamber having a predetermined first width, first length and first depth;
a three-dimensional gel (3D-gel) cell support carrier having a certain degree of solidity made of a hydrogel for a highly biocompatible microenvironment containing predetermined cells in a uniformly distributed manner in the cell culture chambers;
an inlet tank directly connected to the cell culture chamber for supplying a material to the cell culture chamber through a first opening; and
an outlet tank directly connected to the cell culture chamber for removing the material from the cell culture chamber through a second opening, wherein the inlet is larger than the outlet while both the inlet and the outlet are larger than the cell culture chamber.