IP Library › Granted Patent US 9,074,188
Granted Patent B2
US 9,074,188 · App. 13/885,515 · Granted Jul 7, 2015

Cardiomyocyte- and/or cardiac progenitor cell-proliferating agent and method for proliferating cardiomyocytes and/or cardiac progenitor cells

Inventors: Jun Yamashita (Kyoto, JP); Hideki Uosaki (Kyoto, JP)
Assignee: KYOTO UNIVERSITY
C12N5/0657C12N2501/415C12N5/0662C12N2501/70C12N2501/999C12N2503/02G01N33/5061
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,074,188
App. No.
13/885,515
Granted
Jul 7, 2015
Kind
B2
Abstract

A method for proliferating cardiomyocytes and/or cardiac progenitor cells is disclosed. The proliferation method includes contact with at least one compound such as a GSK3β inhibitor, ERK dephosphorylation inhibitor, Raf activator, CaMK2 inhibitor and p38 inhibitor. The cardiomyocyte and the cardiac progenitor cell may be a human cardiomyocyte or human cardiac progenitor cell and may be obtained from differentiation of induced pluripotent stem cells.

Claims (11)

1. A method for proliferating cardiomyocytes and/or cardiac progenitor cells, comprising contacting cultured cardiomyocytes and/or cardiac progenitor cells with GSK3β inhibitor, and p38 inhibitor, wherein the cardiomyocyte is a human cardiomyocyte and the cardiac progenitor cell is a human cardiac progenitor cell.

2. The method according to claim 1 , wherein said cardiomyocytes and/or cardiac progenitor cells are cardiomyocytes and/or cardiac progenitor cells obtained by differentiation induction of pluripotent stem cells.

3. The method according to claim 1 , wherein said cardiomyocytes and/or cardiac progenitor cells are further contacted with i) CaMK2 inhibitor, and/or ii) ERK activator.

4. The method according to claim 3 , wherein said CaMK2 inhibitor is KN62 or KN93, and said ERK dephosphorylation inhibitor is SU1498.

5. The method according to claim 1 , wherein expression of CyclinA2, CyclinD2, CyclinD3, Cdk2 and cdk4 is enhanced and expression of Ink4b is decreased in cardiomyocytes and/or cardiac progenitor cells after contacting cardiomyocytes and/or cardiac progenitor cells with GSK3 beta inhibitor, and p38 inhibitor.

6. The method according to claim 1 , wherein said GSK3β inhibitor is CHIR99021 or BIO and said p38 inhibitor is SB203580.

7. A method for screening a cardiomyocyte- and/or cardiac progenitor cell-proliferating agent, comprising the steps of:

(1) contacting a test substance with cardiomyocytes and/or cardiac progenitor cells obtained by differentiation induction of pluripotent stem cells;

(2) counting the number of cardiomyocytes and/or cardiac progenitor cells after step (1); and

(3) selecting the test substance as a cardiomyocyte- and/or cardiac progenitor cell-proliferating agent when the number of cardiomyocytes and/or cardiac progenitor cells is equivalent to or larger than the number of cardiomyocytes and/or cardiac progenitor cells which are contacted with a positive control agent having cardiomyocyte- and/or cardiac progenitor cell-proliferating ability, wherein the cardiomyocyte is a human cardiomyocyte and the cardiac progenitor cell is a human cardiac progenitor cell,

and wherein said positive control agent is at least one compound selected from the group consisting of ERK dephosphorylation inhibitor, Raf activator, and CaMK2 inhibitor.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2013
From: YAMASHITA, JUN; UOSAKI, HIDEKI
To: KYOTO UNIVERSITY
Reel/Frame 030434/0956 →
Continuity (2)
Provisional Application 61414812 · Nov 17, 2010
Related Publication 20130244262A1 · Sep 19, 2013