Isolation of bona fide pancreatic progenitor cells

• US 10,494,608 B2
• Filed: 04/21/2016
• Issued: 12/03/2019
• Est. Priority Date: 04/24/2015
• Status: Active Grant

• Current Assignee: University of Copenhagen
• Original Assignee: University of Copenhagen
• Inventors: Ameri, Jacqueline, Semb, Henrik
• Primary Examiner(s): Gamett, Daniel C
• Application Number:
  US15/568,978
• Publication Number:
  US 20180127724A1
• Time in Patent Office: 1,321 Days
• Field of Search: None
• CPC Class Codes: A61P 3/08 for glucose homeostasis pancreatic hormones A61P5/48
• CPC Class Codes: C07K 16/2863 against receptors for growth factors, growth regulators
• CPC Class Codes: C12N 2501/50 Cell markers; Cell surface determinants
• CPC Class Codes: C12N 2501/58 Adhesion molecules, e.g. ICAM, VCAM, CD18 (ligand), CD11 (ligand), CD49 (ligand)
• CPC Class Codes: C12N 2501/585 Integrins
• CPC Class Codes: C12N 2506/02 from embryonic cells
• CPC Class Codes: C12N 5/0081 Purging biological preparations of unwanted cells
• CPC Class Codes: C12N 5/0676 Pancreatic cells
• CPC Class Codes: C12N 5/0678 Stem cells; Progenitor cells; Precursor cells
• CPC Class Codes: G01N 33/566 using specific carrier or receptor proteins as ligand binding reagents where possible specific carrier or receptor proteins are classified with their target compounds

Abstract

The present invention relates to a method for isolating bona fide pancreatic progenitor cells and to cell populations enriched for bona fide pancreatic progenitor cells.

Claims

1. A method for isolating a cell population enriched for bona fide pancreatic progenitor cells, said method comprising:

i) providing a cell population comprising at least one bona fide pancreatic progenitor cell, wherein the bona fide pancreatic progenitor cell expresses PDX1 and NKX6-1; and

ii) exposing said cell population to a ligand which binds to a marker specific for PDX1+ cells, wherein the marker is selected from the group consisting of;

FOLR1, GP2 and MPZ, and selecting the cells that bind to said ligand from the cells that do not bind to said ligand, thereby enriching the cell population for PDX1+ cells, wherein if the marker is GP2 or MPZ, then the PDX1+ cell population is also enriched for PDX1+ NKX6-1+ cells;

thereby obtaining a cell population enriched for bona fide pancreatic progenitor cells.

2. The method according to claim 1, wherein the ligands is an antibody or fragment thereof.

3. The method according to claim 1, wherein the cells are removed or selected by flow cytometry.

4. The method according to claim 2, wherein the ligand is an antibody or fragment thereof directed against GP2.

5. The method according to claim 4, further comprising exposing the cell population to an antibody or fragment thereof directed against CD49d and selecting the cells that do not bind to the antibody or fragment thereof directed against CD49d from the cells that do bind the antibody or fragment thereof directed against CD49d prior to exposing the cell population to an antibody directed against GP2.

6. The method according to claim 1, wherein the bona fide pancreatic progenitor cells are derived from cells capable of differentiation selected from the group consisting of human iPS cells (hIPSCs), human ES cells (hESCs) and naive human stem cells (NhSCs).

7. The method according to claim 6, wherein the cells capable of differentiation are derived from cells isolated from an individual.

8. The method according to claim 1, wherein at least one cell of the cell population enriched for bona fide pancreatic progenitor cells has the capability to differentiate further into pancreatic hormone-producing cells.

9. The method according to claim 1, wherein CDKN1a or CDKN2a is inactivated in the cell population provided in i).

10. The method according to claim 9, wherein CDKN1a and/or CDKN2a is inactivated by knock-down, deletion, silencing or repression.

11. The method according to claim 1, wherein the starting cell population is a pancreatic progenitor population expressing PDX1.

12. The method according to claim 11, wherein inactivation of CDKN1a and/or CDKN2a results in an increase in the proportion of cells entering replicating stage compared to the proportion of cells entering replicating stage when CDKN1a and/or CDKN2a is not inactivated.

13. The method according to claim 12, wherein the increase is at least 1.5-fold.

14. A method for producing a cell population enriched for bona fide pancreatic progenitor cells, said enriched cell population comprising at least 70% bona fide pancreatic progenitor cells, comprising the method according to claim 1.

15. The method of claim 14, said method comprising:

i) providing a cell population comprising a bona fide pancreatic progenitor cell, wherein the bona fide pancreatic progenitor cell expresses PDX1 and NKX6-1; and

ii) exposing said cell population to;

a) a ligand which binds to a marker specific for PDX1+ cells and selecting the cells that bind to said ligand from the cells that do not bind to said ligand, thereby enriching the cell population for PDX1+ cells, wherein the marker is selected from the group consisting of;

FOLR1, GP2 and MPZ,

thereby enriching the cell population for PDX1+ cells, wherein if the marker is GP2 or MPZ, then the PDX1+ cell population is also enriched for PDX1+ NKX6-1+ cells.

16. The method of claim 15 wherein CDKN1a and/or CDKN2a is inactivated in the cell population provided in i).

17. A method of treatment of a metabolic disorder in an individual in need thereof, wherein the method comprises providing a cell population enriched for bona fide pancreatic progenitor cells according to the method of claim 1.

18. The method according to claim 17, said method further comprising transplanting at least part of said cell population into said individual.

19. The method according to claim 17, said method further comprising inducing differentiation of at least part of cell population into insulin-producing cells and isolating said insulin-producing cells.

20. The method according to claim 19, said method further comprising transplanting said insulin-producing cells into said individual.