Cell culture devices having ultrathin porous membrane and uses thereof

• US 8,119,394 B2
• Filed: 03/14/2007
• Issued: 02/21/2012
• Est. Priority Date: 03/14/2006
• Status: Active Grant

• Current Assignee: University of Rochester
• Original Assignee: University of Rochester
• Inventors: McGrath, James L., Gaborski, Thomas R., Striemer, Christopher C., Fauchet, Philippe M.
• Primary Examiner(s): Beisner, William H
• Application Number:
  US11/686,196
• Publication Number:
  US 20070231887A1
• Time in Patent Office: 1,805 Days
• Field of Search: 435/297.5, 435/297.1
• US Class Current: 435/297.1
• CPC Class Codes: B01L 2300/0681 Filter
• CPC Class Codes: B01L 3/502 with fluid transport, e.g. in multi-compartment structures centrifugal-type cuvettes G01N21/07; analysis by separation into components G01N30/00; automatic analysers G01N35/00
• CPC Class Codes: C12M 23/12 Well or multiwell plates C12M25/04 takes precedence
• CPC Class Codes: C12M 23/34 Internal compartments or partitions
• CPC Class Codes: C12M 25/14 Scaffolds; Matrices in general C12N5/0068
• CPC Class Codes: C12M 29/04 Filters; Permeable or porous membranes or plates, e.g. dialysis
• CPC Class Codes: C12M 35/08 Chemical, biochemical or biological means, e.g. plasma jet, co-culture

Abstract

Disclosed is a device for co-culturing two or more populations of cells using ultrathin, porous membranes positioned between cell culture chambers. Multiple chamber devices and uses thereof are described, including the formation of in vitro tissue models for studying drug delivery, cell-cell interactions, and the activity of low abundance molecular species.

Claims

1. A cell culture device comprising:

first and second chambers separated by at least one nanoscale semiconductor membrane positioned between the first and second chambers, the at least one nanoscale membrane having an average thickness of less than about 100 nm, and having a plurality of pores extending between opposite sides thereof.

2. The device according to claim 1 further comprising cell culture medium in the first and second chambers, a first cell type in the first chamber, and a second cell type in the second chamber.

3. The device according to claim 1, wherein the device comprises a plurality of first chambers and one second chamber in communication with each of the plurality of first chambers through the at least one nanoscale membrane.

4. The device according to claim 3 further comprising cell culture medium in the plurality of first chambers and the one second chamber.

5. The device according to claim 4 further comprising a first cell type in each of the plurality of first chambers.

6. The device according to claim 5 further comprising a second cell type in the one second chamber.

7. The device according to claim 4 further comprising two or more different cell types separately residing in the plurality of first chambers.

8. The device according to claim 7 further comprising a further cell type in the one second chamber.

9. The device according to claim 1, wherein the device comprises a plurality of paired first and second chambers, with each second chamber in communication with only one first chamber through the at least one nanoscale membrane.

10. The device according to claim 9 further comprising cell culture medium in the plurality of paired first and second chambers, a first cell type in the first chambers, and a second cell type in the second chambers.

11. The device according to claim 10, wherein the first cells types are the same in each of the first chambers and the second cell types are the same in each of the second chambers.

12. The device according to claim 10, wherein the first cells types are different in each of the first chambers and the second cell types are the same or different in each of the second chambers.

13. The device according to claim 1 further comprising:

an intermediate chamber positioned between the first and second chambers, the intermediate chamber being separated from each of the first and second chambers by one or more of the at least one nanoscale membranes.

14. The device according to claim 13 wherein the at least one nanoscale membrane separating the first chamber and the intermediate chamber is substantially the same as the at least one nanoscale membrane separating the second chamber and the intermediate chamber.

15. The device according to claim 13 wherein the at least one nanoscale membrane separating the first chamber and the intermediate chamber is different from the at least one nanoscale membrane separating the second chamber and the intermediate chamber.

16. The device according to claim 13 further comprising cell culture medium in the first, second, and intermediate chambers.

17. The device according to claim 16 further comprising a first cell type in the first chamber and a second cell type in the second chamber.

18. The device according to claim 17 further comprising a third cell type in the intermediate chamber.

19. The device according to claim 1, wherein at least one of the chambers comprises a three-dimensional scaffold.

20. The device according to claim 1, wherein the at least one nanoscale membrane precludes cell-to-cell contact between cells grown on opposite sides thereof.

21. The device according to claim 1, wherein the at least one nanoscale membrane promotes cell-to-cell contact between cells grown on opposite sides thereof.

22. The device according to claim 1, wherein the at least one nanoscale membrane comprises a plurality of spaced nanoscale membranes positioned between the first and second chambers.

23. The device according to claim 22, wherein each of the plurality of nanoscale membranes is characterized by a substantially similar thickness, pore density, and pore dimensions.

24. The device according to claim 22, wherein the plurality of nanoscale membranes includes membranes having different thicknesses, pore densities, and/or pore dimensions.

25. The device according to claim 1, wherein the nanoscale membrane has a pore density of between about 10⁶ and about 10¹² per cm² of membrane.

26. The device according to claim 1, wherein the nanoscale membrane is between about 50 and about 100 nm thick.

27. The device according to claim 1, wherein the nanoscale membrane is between about 10 and about 50 nm thick.

28. The device according to claim 1, wherein the nanoscale membrane is less than about 10 nm thick.

29. The device according to claim 1, wherein the average diameter of the plurality of pores is between about 2 and 50 nanometers.

30. The device according to claim 1, wherein the nanoscale membrane is characterized by an area to thickness aspect ratio that is more than 10,000 to 1.

31. The device according to claim 1, wherein the semiconductor material is selected from the group of silicon, silicon alloys, p-doped silicon, and n-doped silicon.

32. The device according to claim 1, wherein the semiconductor material is in a crystalline form.

33. The device according to claim 1, wherein the nanoscale membrane comprises a cell surface receptor, an antibody, a ligand, a biological reagent, or a combination thereof, within the pores of said membrane.

34. The device according to claim 1 further comprising:

a power source electrically coupled to the nanoscale membrane in a manner effective to charge the membrane.

35. The device according to claim 34, wherein the nanoscale membrane is positively charged.

36. The device according to claim 34, wherein the nanoscale membrane is negatively charged.

37. A sterile package comprising:

a sealed package defining an interior that is sterile; and

a device according to claim 1 positioned within the interior of the sealed package.

38. A kit comprising the device according to claim 1 and one or more of (i) a cell culture medium, (ii) one or more cell lines, and (iii) instructions for co-culturing one or more cells.

39. The kit according to claim 38, wherein the device is sterile and positioned within a sealed package that defines a sterile environment.

40. A method of co-culturing two or more populations of cells comprising:

providing a device according to claim 1; and

culturing a first population of cells in a first chamber and a second population of cells in a second chamber.

41. The method according to claim 40, wherein said cells are physically separated yet are able to contact and/or communicate with each other through said plurality of pores.

42. The method according to claim 40, wherein said cells are able to communicate but not contact one another through said plurality of pores.

43. The method according to claim 40, wherein said populations of cells physically contact each other through said plurality of pores.

44. The method according to claim 40, wherein said population of cells are derived from an animal, bacteria, fungus, yeast, algae, and/or plant.

45. A method of visualizing cells comprising:

providing a cell culture device according to claim 1 with cells in the first and/or second chambers; and

observing the cells of the first and/or second chambers via microscopy.

46. The method according to claim 45 further comprising fixing the cells of the first and second chambers prior to said observing.

47. The method according to claim 45 further comprising staining and/or labeling cells prior to said observing.

48. The method according to claim 45, wherein said observing is carried out by light microscopy, Darkfield microscopy, Brightfield microscopy, differential interference contrast microscopy, phase contrast microscopy, polarized light microscopy, confocal microscopy, near-field scanning optical microscopy, fluorescence microscopy, scanning electron microscopy, or transmission electron microscopy.

49. A method of monitoring low abundance molecular species comprising:

providing a cell culture device according to claim 1 with cells in the first chamber; and

detecting the presence of low abundance molecular species in the second chamber.

50. The method according to claim 49 further comprising:

fixing the cells prior to said detecting.

51. The method according to claim 49 further comprising:

staining and/or labeling the low abundance molecular species or a detection reagent prior to said detecting.