Inverse patterning process for three-dimensional multi-compartmental micro-organization of multiple cell types
The invention features an “inverse patterning” or “Intaglio-Void/Embed-Relief Topographic (In VERT) molding” manufacturing process for generating high-resolution three-dimensional (3D) multi-cellular microstructures in distinct cellular compartments of a single hydrogel. The platform has general utility in the development of engineered tissues for human therapies, drug testing, and disease models. Additionally, the platform can serve as a model system for studying 3D cell-cell interactions in fields as diverse as stem cell biology to the development of cancer therapeutics.
1. A method of making a three-dimensional, multiple cell type tissue construct, comprising
introducing a first population of cells into recessed features of a patterned cell capture substrate;
encapsulating said first cell population in a first polymerizable biomaterial;
polymerizing said first polymerizable biomaterial;
removing and inverting said encapsulated first cell population thereby exposing an inverse pattern of the recessed features containing the first cell population in the first polymerizable biomaterial;
contacting the inverse pattern of the recessed features comprising the, first cell population with a second population of cells in a second polymerizable biomaterial;
encapsulating said second population in said second polymerizable biomaterial; and
polymerizing said second polymerizable biomaterial,
such that the three-dimensional, multiple cell type tissue construct is made.
2. The method of claim 1 , wherein said first population of cells is incubated under conditions sufficient for formation of cell-cell junctions between cells in said features of said patterned cell capture substrate prior to encapsulating said first cell population in said first polymerizable biomaterial.
3. The method of claim 1 , wherein the patterned cell capture substrate consists of polydimethyl siloxane (PDMS) comprising micro-scale features.
4. The method of claim 1 , wherein the first population of cells is introduced into the features of the patterned cell capture substrate in a media or pre-polymer solution.
5. The method of claim 1 , wherein said first population of cells is incubated for a period of about 6 to about 24 hours, to permit formation of cell-cell junctions between said cells.
6. The method of claim 1 , wherein said first and/or second polymerizable biomaterial is a hydrogel material.
7. The method of claim 6 , wherein the hydrogel material is agarose, fibrin, or polyethylene hydrogel.
8. The method of claim 7 , wherein the hydrogel material is photopolymerized polyethylene glycol (PEG) hydrogel.
9. The method of claim 1 , wherein the first or second cell population, or both the first and second cell populations comprise parenchymal cells.
10. The method of claim 1 , wherein the first or second cell population, or both the first and second cell populations comprise non-parenchymal cells.
11. The method of claim 1 , wherein the first or second cell population, or both the first and second cell populations comprise a combination of parenchymal and non-parenchymal cells.
12. The method of claim 9 , wherein the parenchymal cells are human parenchymal cells.
13. The method of claim 5 , wherein the hydrogel is derivatized with one or more cell-adhesive peptides, or comprises one or more soluble factors supporting cell growth and/or differentiation.
14. The method of claim 1 , wherein the first or second cell populations, or both the first and second cell populations are encapsulated at a concentration of from about 8×10 6 cells/ml to about 24×10 6 cells/ml.
15. The method of claim 1 , wherein the polymerizable biomaterial is biodegradable.
16. The method of claim 1 , wherein one or more of the populations of cells is engineered to express a reporter protein.
17. The method of claim 1 , wherein said first population of cells is incubated for a period of about 8 to about 16 hours to permit formation of cell-cell junctions between said cells.
18. The method of claim 1 , wherein said first population of cells is incubated for a period of about 12 hours to permit formation of cell-cell junctions between said cells.