IP Library Granted Patent US 8,603,811
Granted Patent B2
US 8,603,811 · App. 13/275,274 · Granted Dec 10, 2013

Endocrine precursor cells, pancreatic hormone-expressing cells and methods of production

Inventors: Kevin A. D'Amour (San Diego, CA); Anne Bang (San Diego, CA); Emmanuel E. Baetge (Encinitas, CA)
Assignee: ViaCyte, Inc.
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Quick Facts
Patent No.
US 8,603,811
App. No.
13/275,274
Granted
Dec 10, 2013
Kind
B2
Abstract

Disclosed herein are cell cultures and enriched cell populations of endocrine precursor cells, immature pancreatic hormone-expressing cells and mature pancreatic hormone-expressing cells. Also disclosed herein are methods of producing such cell cultures and cell populations.

Claims (26)

1. A first and second cell population comprising:

a) a first in vitro cell population comprising human pluripotent cells; and

b) a second in vitro cell population comprising progeny of a portion of the first cell population, wherein the progeny comprise at least 5% endocrine precursor cells that express a marker selected from the group consisting of neurogenin 3 (NEUROG3), paired box 4 (PAX4) and NKX2 transcription factor related locus 2 (NKX2.2).

2. The first and second cell population of claim 1 , wherein said endocrine precursor cells are multipotent cells that can differentiate into pancreatic islet hormone-expressing cells that express at least one pancreatic hormone selected from the group consisting of insulin, somatostatin, ghrelin, pancreatic polypeptide and glucagon.

3. The first and second cell population of claim 1 , wherein said endocrine precursor cells express NEUROG3, PAX4 and NKX2.2.

4. The first and second cell population of claim 1 , wherein the progeny comprise at least 50% endocrine precursor cells.

5. The first and second cell population of claim 1 , wherein said endocrine precursor cells do not substantially express a pancreatic hormone selected from the group consisting of ghrelin, insulin, somatostatin and glucagon.

6. The first and second cell population of claim 1 , wherein said endocrine precursor cells are non-recombinant cells.

7. The first and second cell population of claim 1 , wherein said endocrine precursor cells express NCAM.

8. The first and second cell population of claim 1 , wherein said endocrine precursor cells comprise a reagent bound to NCAM.

9. The in vitro cell culture of claim 8 , wherein said reagent comprises a molecule selected from the group consisting of an anti-NCAM antibody, an anti-NCAM antibody fragment and an NCAM ligand.

10. The first and second cell population of claim 9 , wherein said reagent is an anti-NCAM antibody.

11. The first and second cell population of claim 10 , wherein said anti-NCAM antibody is labeled.

12. The first and second cell population of claim 1 , wherein said first in vitro cell population comprises at least 10% human pancreatic duodenal homeobox 1 (PDX1)-positive pancreatic endoderm cells.

13. The first and second cell population of claim 1 , wherein said first in vitro cell population comprises at least 50% human pancreatic duodenal homeobox 1 (PDX1)-positive pancreatic endoderm cells.

14. The first and second cell population of claim 1 , wherein the first in vitro cell population further medium-comprises a factor selected from retinoic acid (RA) and exendin 4 (Ex4).

15. A first and second cell population comprising

a) a first in vitro cell population comprising human pluripotent cells; and

b) a second in vitro cell population comprising progeny of a portion of the first cell population, wherein the progeny are obtained by:

(1) providing said first in vitro cell population with a TGFβ superfamily growth factor;

(2) withdrawing the TGFβ superfamily growth factor from said cell population;

(3) providing said cell population with a retinoid; and

(4) incubating said cell population in a culture medium for a sufficient time to permit formation of human endocrine precursor cells expressing a marker selected from the group consisting of neurogenin 3 (NEUROG3), paired box 4 (PAX4) and NKX2 transcription factor related locus 2 (NKX2.2).

16. The first and second cell population of claim 15 , wherein step (2) further comprises providing said cell population with FGF.

17. The first and second cell population of claim 15 , wherein said retinoid comprises retinoic acid.

18. The first and second cell population of claim 15 , wherein step (4) further comprises providing said cell population with a gamma secretase inhibitor.

Continuity (5)
Division 11681687 · Mar 2, 2007
Provisional Application 60852878 · Oct 18, 2006
Provisional Application 60833633 · Jul 26, 2006
Provisional Application 60778649 · Mar 2, 2006
Related Publication 20120034692A1 · Feb 9, 2012