Engineered platforms to stabilize both hepatocytes and endothelial cells in vitro
The disclosure relates to in vitro cultures of human hepatocytes, and in particular co-cultures systems including human hepatocytes, non-parenchymal cells, and human endothelial cells, and the use of the co-cultures in developing and screening drugs.
1. A composition comprising a population of human hepatocytes, a population of murine embryonic fibroblasts, and a population of human endothelial cells selected from human primary liver sinusoidal endothelial cells (LSECs) or human umbilical vein endothelial cells (HUVECs) in co-culture in vitro,
wherein the hepatocytes are disposed in a micropattern on a culture substrate,
wherein the micropattern comprises a predetermined two-dimensional pattern of multiple microdots, the micropattern defined by a microdot diameter and an edge-to-edge spacing between each of any two neighboring microdots, and
wherein the hepatocytes occupy the microdots, the murine embryonic fibroblasts occupy the inter-microdot space, and the population of human endothelial cells is positioned on top of a layer of material comprising at least one extracellular matrix protein that is disposed on the population of human hepatocytes and the population of murine embryonic fibroblasts.
2. The composition of claim 1 , further comprising fibronectin.
3. The composition of claim 1 , wherein the human hepatocytes are primary human hepatocytes.
4. The composition of claim 1 , wherein the human hepatocytes are derived from pluripotent stems cells.
5. The composition of claim 4 , wherein the human hepatocytes are derived from induced pluripotent human stem cells.
6. A method of culturing a population of human hepatocytes in vitro, comprising co-culturing the population of human hepatocytes with a population of murine embryonic fibroblasts, and a population of human endothelial cells selected from human primary liver sinusoidal endothelial cells (LSECs) or human umbilical vein endothelial cells (HUVECs),
wherein the hepatocytes are disposed in a micropattern on a culture substrate,
wherein the micropattern comprises a predetermined two-dimensional pattern of multiple microdots, the micropattern defined by a microdot diameter and an edge-to-edge spacing between each of any two neighboring microdots,
wherein the hepatocytes occupy the microdots, the murine embryonic fibroblasts occupy the inter-microdot space, and the population of human endothelial cells is cultured on top of a layer of material comprising at least one extracellular matrix protein that is disposed on the population of human hepatocytes and the population of murine embryonic fibroblasts.
7. The method of claim 6 , further comprising co-culturing the population of human hepatocytes with the population of murine embryonic fibroblasts and the population of human endothelial cells with fibronectin.
8. The method according to claim 6 , wherein the human hepatocytes are primary human hepatocytes.
9. The method according to claim 6 , wherein the human hepatocytes are derived from pluripotent stems cells.
10. The method according to claim 6 , wherein the human hepatocytes are derived from induced pluripotent human stem cells.
11. The composition of claim 2 , wherein the fibronectin is disposed on the culture substrate.
12. The method of claim 7 , wherein the fibronectin is disposed on the culture substrate.
13. The method according to claim 1 , wherein the murine embryonic fibroblasts are 3T3-J2 murine embryonic fibroblasts.