IP Library › Granted Patent US 10,208,287
Granted Patent B2
US 10,208,287 · App. 15/308,147 · Granted Feb 19, 2019

CD82-positive cardiac progenitor cells

Inventors: Jun Yamashita (Kyoto, JP); Masafumi Takeda (Kyoto, JP)
Assignee: iHeart Japan Corporation
C12N5/0657A61K35/12C12N5/10C12N2506/45
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Quick Facts
Patent No.
US 10,208,287
App. No.
15/308,147
Granted
Feb 19, 2019
Kind
B2
Abstract

An object of the present invention is to provide a myocardial progenitor cell that is specifically induced to differentiate into a cardiomyocyte, and a method for preparing the myocardial progenitor cell. A method for preparing a CD82-positive cell includes, in sequence, a step (a) of obtaining stem cells, a step (b) of subjecting the stem cells to induction treatment of differentiation into cardiovascular cells, and a step (c) of separating, from the stem cells having been subjected to the induction treatment of differentiation in the step (b), a CD82-positive cell being negative for at least one cell surface marker selected from CD73, CD44, CD105, CD121a, CD18, and CD120a. This method enables preparation of a CD82-positive cell for use as a myocardial progenitor cell.

Claims (29)

1. A composition comprising:

a cell population containing a myocardial progenitor cell that is CD82-positive, and is negative for at least one cell surface marker selected from a group consisting of CD73, CD44, CD105, CD121a, CD18, and CD120a, and

a physiological aqueous solution,

wherein the myocardial progenitor cell is contained in the cell population at a ratio of at least 80%, and

wherein the physiological aqueous solution contains a cryoprotectant.

2. The composition according to claim 1 , wherein the myocardial progenitor cell is a myocardial progenitor cell that is negative for at least one cell surface marker selected from a group consisting of CD7, CD37, CD43, CD144, STRO-1, CD177, and CD163; and/or is positive for at least one cell surface marker selected from a group consisting of CD137L, CD140b, CD180, CD252, CD344, CD118, and CD99R.

3. The composition according to claim 1 , wherein the myocardial progenitor cell is a myocardial progenitor cell that is negative for at least one cell surface marker selected from a group consisting of CD49a, CD117, CD31, CD106, CD45, CD14, HLA-DR, CD38, CD121b, CD122, CD124, CD126, CD127, CD11a, CD104, CD62e, CD621, CD62p, CD120b, CD34, and CD4; and/or is positive for at least one cell surface marker selected from a group consisting of CD166, CD304, and CD90.

4. The composition according to claim 1 , wherein the myocardial progenitor cell is a myocardial progenitor cell that is positive for at least one cell surface marker selected from a group consisting of ROR2

CD13, PDGFRα, and KDR.

5. The composition according to claim 1 , being cryopreserved.

6. A heart disease therapeutic agent comprising the composition according to claim 1 .

7. A method for preparing a myocardial progenitor cell, comprising steps (a) to (c) below,

(a) a step of obtaining pluripotent stem cells;

(b) a step of subjecting the pluripotent stem cells to induction treatment of differentiation into cardiovascular cells; and

(c) a step of isolating, from the pluripotent stem cells having been subjected to the induction treatment of differentiation in the step (b), a myocardial progenitor cell that is CD82-positive, and is negative for at least one cell surface marker selected from a group consisting of CD73, CD44, CD105, CD121a, CD18, and CD120a, using an anti-CD82 antibody.

8. The preparation method according to claim 7 , wherein the pluripotent stem cells are human pluripotent stem cells.

9. The preparation method according to claim 8 , wherein the human pluripotent stem cells are human induced pluripotent stem cells.

10. The preparation method according to claim 7 , wherein the induction treatment of differentiation into cardiovascular cells is induction treatment of differentiation into myocardial progenitor cells.

11. The preparation method according to claim 7 , wherein the myocardial progenitor cell is a myocardial progenitor cell that is negative for at least one cell surface marker selected from a group consisting of CD7, CD37, CD43, CD144, STRO-1, CD177, and CD163; and/or is positive for at least one cell surface marker selected from a group consisting of CD137L, CD140b, CD180, CD252, CD344, CD118, and CD99R.

12. The preparation method according to claim 7 , wherein the myocardial progenitor cell is a myocardial progenitor cell that is negative for at least one cell surface marker selected from a group consisting of CD49a, CD117, CD31, CD106, CD45, CD14, HLA-DR, CD38, CD121b, CD122, CD124, CD126, CD127, CD11a, CD104, CD62e, CD621, CD62p, CD120b, CD34, and CD4; and/or is positive for at least one cell surface marker selected from a group consisting of CD166, CD304, and CD90.

13. The preparation method according to claim 7 , wherein the myocardial progenitor cell is a myocardial progenitor cell that is positive for at least one cell surface marker selected from a group consisting of ROR2

CD13, PDGFRα, and KDR.

14. The preparation method according to claim 7 , wherein, in the step (c), the myocardial progenitor cell is isolated during day 4 to day 8 after the induction treatment of differentiation performed in the step (b).

15. The composition according to claim 2 , wherein the myocardial progenitor cell is a myocardial progenitor cell that is negative for at least one cell surface marker selected from a group consisting of CD49a, CD117, CD31, CD106, CD45, CD14, HLA-DR, CD38, CD121b, CD122, CD124, CD126, CD127, CD11a, CD104, CD62e, CD621, CD62p, CD120b, CD34, and CD4; and/or is positive for at least one cell surface marker selected from a group consisting of CD166, CD304, and CD90.

16. The composition according to claim 2 , wherein the myocardial progenitor cell is a myocardial progenitor cell that is positive for at least one cell surface marker selected from a group consisting of ROR2

CD13, PDGFRα, and KDR.

17. The composition according to claim 3 , wherein the myocardial progenitor cell is a myocardial progenitor cell that is positive for at least one cell surface marker selected from a group consisting of ROR2, CD13, PDGFRα, and KDR.

18. The composition according to claim 15 , wherein the myocardial progenitor cell is a myocardial progenitor cell that is positive for at least one cell surface marker selected from a group consisting of ROR2, CD13, PDGFRα, and KDR.

19. The preparation method according to claim 7 , wherein, in the step (c), the myocardial progenitor cell is isolated so that the myocardial progenitor cell is contained in a cell population at a ratio of at least 80%.

Assignments (5)
CHANGE OF ADDRESS Recorded Mar 30, 2023
From: IHEART JAPAN CORPORATION
To: IHEART JAPAN CORPORATION
Reel/Frame 063190/0655 →
CORRECTION BY DECLARATION OF INCORRECT RECORDATION FOR US APPLICATION 15/308,147 RECORDED AT REEL/FRAME 050096/0945 Recorded Mar 3, 2021
From: IHEART JAPAN CORPORATION
To: IHEART JAPAN CORPORATION
Reel/Frame 055816/0534 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 20, 2019
From: KYOTO UNIVERSITY MEDICAL INNOVATION CENTER
To: KYOTO UNIVERSITY MED-PHARM COLLABORATION BUILDING
Reel/Frame 050096/0945 →
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY'S ADDRESS PREVIOUSLY RECORDED AT REEL: 040185 FRAME: 0161. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Nov 22, 2016
From: YAMASHITA, JUN; TAKEDA, MASAFUMI
To: IHEART JAPAN CORPORATION
Reel/Frame 040672/0338 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2016
From: YAMASHITA, JUN; TAKEDA, MASAFUMI
To: IHEART JAPAN CORPORATION
Reel/Frame 040185/0161 →
Priority Claims (1)
JP 2014-094775 · May 1, 2014 · national
Continuity (1)
Related Publication 20170067023A1 · Mar 9, 2017