Composition and method for enabling proliferation of pluripotent human stem cells
Compositions and processes for culturing human stem cells in vitro in an undifferentiated state are disclosed. In this regard, human embryonic stem cells proliferated and maintained their pluripotency when cultured on plates coated with recombinant laminin-10 (laminin-511).
1. A method for creating a new pluripotent human stem cell line in a defined and xeno-free environment comprising:
providing a substrate comprising a coating that is devoid of both animal proteins and feeder cells, and the coating comprises a single isoform of a full-length laminin consisting of laminin-511 (LN-511 or laminin-10);
plating cells from a blastocyst inner cell mass comprising pluripotent human stem cells onto the coating;
exposing the pluripotent human stem cells to a chemically defined medium that is devoid of feeder cells; and
obtaining a new pluripotent human stem cell line from outgrowth of the human stem cells.
2. The method of claim 1 , wherein the new pluripotent human stem cell line is non-differentiated.
3. The method of claim 1 , wherein the new pluripotent human stem cell line is homogeneous.
4. The method of claim 1 , wherein the new pluripotent human stem cell line forms monolayers on the coating.
5. The method of claim 1 , wherein the new pluripotent human stem cell line comprises non-differentiated embryonic stem cells.
6. The method of claim 1 , further comprising:
harvesting the new pluripotent human stem cell line;
replating the new pluripotent human stem cell line on a second substrate comprising the coating;
exposing the new pluripotent human stem cell line to a chemically defined medium that is devoid of feeder cells; and
obtaining refined pluripotent human stem cells from outgrowth of the new pluripotent human stem cell line.
7. The method of claim 1 , wherein the medium further comprises a growth factor.
8. A method for maintaining self-renewing pluripotent human stem cells, comprising:
a) providing a substrate comprising a coating that is devoid of both animal proteins and feeder cells, and the coating comprises only a single isoform of a laminin consisting of intact laminin-511 (LN-511 or laminin-10);
b) plating pluripotent human stem cells onto the coating;
c) exposing the pluripotent human stem cells to a chemically defined medium that is devoid of feeder cells, thereby maintaining self-renewing pluripotent human stem cells; and
d) periodically harvesting and replating the pluripotent human stem cells.
9. The method of claim 8 , wherein the medium further comprises a growth factor.
10. The method of claim 8 , wherein the pluripotent human stem cells from step c) form monolayers on the coating.
11. The method of claim 8 , wherein the pluripotent human stem cells are non-differentiated embryonic stem cells.