Implantable human liver tissue constructs and uses thereof
Engineered human tissue constructs are provided that are suitable for use in making humanized animals for use in pharmaceutical development. Humanized animals having the constructs implanted in vivo are provided. Methods of making and using the tissue-engineered constructs and humanized animals are also provided.
1. An implantable human liver tissue construct, comprising:
(a) a biocompatible, porous hydrogel scaffold comprising one or more cell adhesive peptides,
(b) a population of cells comprising human hepatocytes and non-parenchymal cells seeded on the hydrogel scaffold of (a), wherein the non-parenchymal cells support hepatocellular viability and function; and
(c) a population of cells comprising human liver-derived non-parenchymal cells seeded on the hydrogel scaffold of (a),
wherein the cell populations of (b) and (c) are encapsulated in (a) in a pattern to prevent physical contact between the cell populations of (b) and (c).
2. The construct of claim 1 , wherein the hepatocytes are infected with a human liver-trophic pathogen.
3. The construct of claim 2 , wherein the human liver-trophic pathogen is a virus or a parasite.
4. The construct of claim 3 , wherein the virus is HCV or malaria.
5. The construct of claim 1 , wherein the hydrogel is photopolymerized polyethylene glycol (PEG) hydrogel.
6. The construct of claim 5 , wherein the photopolymerized polyethylene glycol (PEG) hydrogel is a polyethylene glycol-diacrylate (PEG-DA) hydrogel.
7. The construct of claim 1 , wherein the non-parenchymal cells are stromal cells.
8. The construct of claim 7 , wherein the stromal cells are fibroblasts.
9. The construct of claim 1 , wherein the hydrogel contains about 8×10 6 hepatocytes/ml.
10. The construct of claim 8 , wherein the hydrogel contains about 15-25×10 6 fibroblasts/ml.
11. The construct of claim 1 , wherein the human liver-derived non-parenchymal cells are human liver endothelial cells (LECs).
12. The construct of claim 11 , wherein the hydrogel contains about 6×10 6 LECs/ml.
13. The construct of claim 11 , wherein the LECs are TMNK-1 cells.
14. The construct of claim 1 , wherein maintenance of hepatocellular viability and function is evidenced by albumin secretion or urea synthesis at levels of at least about 90% relative to starting levels.
15. The construct of claim 1 , wherein maintenance of hepatocellular viability and function is evidenced by drug metabolism enzyme expression or function at levels of about 90% relative to starting levels.
16. The construct of claim 1
(a) wherein the construct has a diameter of about 20-mm and a thickness of about 250 μm, the construct comprising about 0.5×10 6 human hepatocytes;
(b) wherein the hydrogel comprises perfusion channels supporting diffusive transport of oxygen and nutrients;
(c) wherein the scaffold is non-biodegradable; and
(d) wherein the cell-adhesive peptide is an extracellular matrix- (ECM-) derived peptide, optionally covalently attached to a component of the hydrogel.
17. The construct of claim 1 , wherein the construct remains viable for at least three, four, six, eight or twelve weeks upon in vivo implantation.
18. The construct of claim 1 , wherein the ECM-derived peptide is an RGDS peptide.
19. The construct of claim 1 , wherein the construct is explantable.
20. The construct of claim 1 , wherein
(a) the construct has a diameter or width of about 5-50 mm; and
(b) the construct has a thickness of about 50-1000 μm.
21. The construct of claim 1 , wherein
(a) the construct has a diameter or width of about 5-50 mm;
(b) the construct has a thickness of about 50-1000 μm; and
(c) the construct comprises about 1 to 50×10 6 human hepatocytes/ml.
22. The construct of claim 1 , wherein the construct has a diameter of about 20-mm and a thickness of about 250 μm, and wherein the construct comprises about 0.5×10 6 human hepatocytes.
23. The construct of claim 1 , wherein the hydrogel comprises perfusion channels supporting diffusive transport of oxygen and nutrients.
24. The construct of claim 1 , wherein the scaffold is non-biodegradable.
25. The construct of claim 1 , wherein the cell-adhesive peptide is an extracellular matrix- (ECM-) derived peptide covalently attached to a component of the hydrogel.
26. The construct of claim 25 , wherein one or more of the populations of cells is engineered to express a reporter protein.
27. The construct of claim 1 , wherein the ECM-derived peptide is an RGDS peptide covalently attached to an acrylate PEG monomer polymerized in the hydrogel.
28. The construct of claim 1 , wherein the hydrogel is patterned to permit diffusion of oxygen and nutrients to the innermost cells.
29. The construct of claim 1 , wherein the hepatocytes are primary hepatocytes, progenitor-derived, ES-derived, or induced pluripotent stem cell-derived.
30. The construct of claim 1 , wherein the non-parenchymal cells are fibroblasts and the human liver-derived non-parenchymal cells are endothelial cells.
31. The construct of claim 29 , wherein the non-parenchymal cells are fibroblasts and the human liver-derived non-parenchymal cells are endothelial cells.
32. The construct of claim 30 , further comprising more than one population of fibroblasts.
33. The construct of claim 30 , wherein the fibroblasts are normal human fibroblasts.
34. The construct of claim 1 , further comprising at least one other cell type.
35. The construct of claim 34 , wherein the at least one cell type is a liver cell type selected from the group consisting of Kupffer cells, Ito cells, and biliary ductal cells.
36. The construct of claim 34 , wherein the at least one cell type is an immune cell type selected from the group consisting of macrophages, B-cells, and dendritic cells.
37. The construct of claim 1 , wherein the hepatocytes are a combination of hepatocytes and liver cells.
38. A method of making an implantable human liver tissue construct, comprising
obtaining a co-culture comprising a population of human hepatocytes, a population of non-parenchymal cells supporting hepatocellular viability and function, and a population of human liver-derived non-parenchymal cells, wherein the co-culture has been previously cultured in vitro for a time sufficient to stabilize hepatocyte function; and
encapsulating the co-culture in a biocompatible, hydrogel scaffold comprising one or more cell-adhesive peptides, wherein the population of liver-derived non-parenchymal cells are encapsulated in a pattern to prevent physical contact between the hepatocytes and the non-parenchymal cells.
39. The method of claim 38 , wherein the hydrogel is photopolymerized polyethylene glycol (PEG) hydrogel, for example, a polyethylene glycol-diacrylate (PEG-DA) hydrogel.
40. The method of claim 39 , wherein the non-parenchymal cells are stromal cells.
41. The method of claim 39 , wherein the hydrogel contains about 8×10 6 hepatocytes/ml.
42. The method of claim 40 , wherein the stromal cells are fibroblasts and the hydrogel contains about 24×10 6 fibroblasts/ml.
43. The method of claim 38 , wherein the human liver-derived non-parenchymal cells are human liver endothelial cells (LECs), and wherein the hydrogel contains about 6×10 6 LECs/ml.
44. The method of claim 38 , wherein
(a) the construct has a diameter of about 20-mm and a thickness of about 250 μm, the construct comprising about 0.5×10 6 human hepatocytes;
(b) the hydrogel comprises perfusion channels supporting diffusive transport of oxygen and nutrients;
(c) the scaffold is non-biodegradable; and
(d) the cell-adhesive peptide is an extracellular matrix- (ECM-) derived peptide, optionally covalently attached to a component of the hydrogel.
45. The method of claim 38 , wherein the construct remains viable for at least three, four, six, eight or twelve weeks upon in vivo implantation or wherein one or more of the populations of cell is engineered to express a reporter protein.
46. The method of claim 40 , wherein the stromal cells are fibroblasts.
47. The method of claim 43 , wherein the LECs are TMNK-1 cells.
48. The method of claim 44 , wherein the ECM-derived peptide is an RGDS peptide, optionally covalently attached to an acrylate PEG monomer polymerized in the hydrogel.