IP Library Granted Patent US 9,447,378
Granted Patent B2
US 9,447,378 · App. 13/873,020 · Granted Sep 20, 2016

Method for differentiating human embryonic stem cells into β-cells for the treatment of type I diabetes

Inventors: Clark K. Colton (Newton, MA); Amanda Dilenno (Boston, MA); Jeffrey R. Millman (St. Louis, MA)
Assignee: Massachusetts Institute of Technology
C12N5/0606C12N5/0676C12N2500/02C12N2506/02
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Quick Facts
Patent No.
US 9,447,378
App. No.
13/873,020
Granted
Sep 20, 2016
Kind
B2
Abstract

The invention provides inter alia methods for differentiating embryonic stem cells into insulin producing cells, as well as compositions comprising such cells, and therapeutic uses of such compositions.

Claims (21)

1. A method for producing insulin+ and/or C-peptide+ cells, comprising

(1) differentiating human pluripotent stern cells to posterior foregut endoderm in vitro, at an oxygen partial pressure to which cells are exposed (pO 2 cell ) that is greater than 7 mmHg and less than 142 mmHg, in the presence of a TGF-β superfamily member and a retinoic acid receptor agonist, and

(2) differentiating posterior foregut endoderm to insulin+ and/or C-peptide+ cells at a pO 2 cell that is 142 mmHg or higher.

2. The method of claim 1 , wherein the human pluripotent stem cells are differentiated on an oxygen permeable membrane.

3. The method of claim 2 , wherein the oxygen permeable membrane is an oxygen permeable silicone rubber membrane.

4. The method of claim 2 , wherein the oxygen permeable silicone rubber membrane is coated with extracellular matrix (ECM).

5. The method of claim 1 , wherein the iman pluripotent stem cells are human embryonic stem cells.

6. A method for producing insulin+ and/or C-peptide+ cells comprising

(1) differentiating human pluripotent stem cells to definitive endoderm in the presence of a TGF-β superfamily member at a pO 2cell that is in a range of 7 mmHg to 57 mmHg,

(2) differentiating definitive endoderm to posterior foregut endoderm in the presence of a retinoic acid receptor antagonist at a pO 2cell that is in a range of 21 mmHg to 71 mmHg, and

(3) differentiating posterior foregut endoderm to insulin+ and/or C-peptide+ cells at a pO 2cell that is 142 mmHg or higher.

7. The method of claim 6 , wherein the the pO 2cell of step (1) is 36 mmHg.

8. The method of claim 6 , wherein the pO 2cell of step (2) is 36 mmHg.

9. The method of claim 6 , wherein the the pO 2cell of step (3) is 142 mmHg.

10. The method of claim 6 , wherein the the pO 2cell of step (3) is higher than 142 mmHg.

11. The method of claim 1 , wherein the pO 2cell of step (1) 36 mmHg.

12. The method of claim 6 , wherein the human pluripotent stem cells are human embryonic stem cells.

13. The method of claim 1 , wherein the pO 2cell of step (1) is 7 mmHg to 57 mmHg.

14. The method of claim 1 , wherein the pO 2cell of step (1) is 21 mmHg to 57 mmHg.

15. The method of claim 1 , wherein the pO 2cell of step (2) is 142 mmHg.

16. The method of claim 1 , wherein the pO 2cell of step (2) is higher than 142 mmHg.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 2, 2013
From: COLTON, CLARK K.; DIIENNO, AMANDA; MILLMAN, JEFFREY R.
To: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
Reel/Frame 030931/0133 →
CONFIRMATORY LICENSE Recorded Jul 11, 2013
From: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 030786/0539 →
Continuity (2)
Provisional Application 61639794 · Apr 27, 2012
Related Publication 20130287743A1 · Oct 31, 2013