Method for preparing induced paraxial mesoderm progenitor (IPAM) cells and their use

Patent metadata

Field	Value
Publication number	US-10240123-B2
Application number	US-201214342251-A
Country	US
Kind code	B2
Filing date	Aug 29, 2012
Priority date	Aug 29, 2011
Publication date	Mar 26, 2019
Grant date	Mar 26, 2019

Abstract

The present invention relates to an ex vivo method for preparing induced paraxial mesoderm progenitor (iPAM) cells, said method comprising the step of culturing pluripotent cells in an appropriate culture medium comprising an effective amount of an activator of the Wnt signaling pathway and an effective amount of an inhibitor of the Bone Morphogenetic Protein (BMP) signaling pathway.

First claim

The invention claimed is:

1. An ex vivo method for preparing a cell population comprising induced human paraxial mesoderm progenitor (iPAM) cells, the method comprising:
culturing human pluripotent cells in a basal culture medium comprising an effective amount of a R-spondin protein or a GSK-3β inhibitor, wherein the culturing results in the production of a human cell population comprising iPAM cells expressing Msgn1 and Tbx6.

2. An ex vivo method for preparing a cell population comprising induced human paraxial mesoderm progenitor (iPAM) cells, the method comprising:
culturing human pluripotent cells selected from the group consisting of human embryonic stem cells or human induced pluripotent stem (iPS) cells, in a basal culture medium comprising an effective amount of a BMP4 inhibitor, and an effective amount of a R-spondin protein or a GSK-3β inhibitor, wherein the culturing results in the production of a human cell population comprising iPAM cells expressing Msgn1 and Tbx6.

3. The ex vivo method according to claim 1 , wherein the R-spondin protein is selected from the group consisting of R-spondin 3, R-spondin 2, and a combination of R-spondin 3 and R-spondin 2.

4. The ex vivo method according to claim 3 , wherein the R-spondin 3 protein is human R-spondin 3 protein encoded by SEQ ID NO: 1, or human R-spondin 3 isoform 2 protein, encoded by SEQ ID NO: 5.

5. The ex vivo method according to claim 3 , wherein the R-spondin 2 protein is human R-spondin 2 encoded by SEQ ID NO: 3, human R-spondin 2 isoform 2, encoded by SEQ ID NO: 6, or human R-spondin 2 isoform 3, encoded by SEQ ID NO: 7.

6. The ex vivo method according to claim 2 , wherein the BMP4 inhibitor is a protein selected from the group consisting of Noggin, Follistatin and Dorsomorphin.

7. The ex vivo method according to claim 6 , wherein the BMP4 inhibitor is Noggin.

8. The ex vivo method according to claim 2 , wherein the BMP4 inhibitor is a chemical inhibitor.

9. The ex vivo method according to claim 1 , wherein the culture medium further comprises DMSO.

10. The ex vivo method according to claim 2 , wherein the basal culture medium further comprises DMSO.

11. The ex vivo method according to claim 1 , wherein the GSK-3β inhibitor is a chemical inhibitor.

12. The ex vivo method according to claim 11 , wherein the GSK-3β inhibitor is CHIR99021 or LiCl.

13. The ex vivo method according to claim 2 , wherein the GSK-3β inhibitor is a chemical inhibitor.

14. The ex vivo method according to claim 13 , wherein the GSK-3β inhibitor is CHIR99021 or LiCl.

15. The ex vivo method according to claim 1 , wherein the basal culture medium further comprises serum or a serum substitute.

16. The ex vivo method according to claim 2 , wherein the basal culture medium further comprises serum or a serum substitute.

Assignees

• Pourquie Olivier
• Chal Jerome
• Inst Nat Sante Rech Med
• Centre Nat Rech Scient
• Univ Strasbourg
• Ass Francaise Contre Le Myopathies

Inventors

• Pourquie Olivier
• Chal Jérôme

Classifications

• C12N5/0654

  Osteocytes, Osteoblasts, Odontocytes; Bones, Teeth · CPC title

• C12N5/0658

  Skeletal muscle cells, e.g. myocytes, myotubes, myoblasts · CPC title

• C12N5/0653

  Adipocytes; Adipose tissue · CPC title

• C12N2501/415

  Wnt; Frizzeled · CPC title

• C12N2506/02

  from embryonic cells · CPC title