Method for inducing cardiac differentiation of pluripotent stem cell with low-molecular compounds

1. A method for inducing cardiac differentiation of a pluripotent stem cell, which comprises the steps of:

(1) culturing a pluripotent stem cell in a medium containing a WNT signaling activator and a PKC activator and

(2) culturing the cell after the step 91) in a medium containing a WNT signaling inhibitor, a Src inhibitor, and an EGFR inhibitor.

2. The method of claim 1 , wherein the WNT signaling inhibitor is a compound of Formula (I):

wherein

R 1 to R 5 are each independently a hydrogen atom; a halogen atom; a hydroxyl group; a linear or branched alkoxy group having 1 to 5 carbon atoms; a linear or branched alkyl group having 1 to 5 carbon atoms which is unsubstituted or substituted with a halogen atom; or a group —NR 12 R 13 , wherein R 12 and R 13 are each independently a hydrogen atom, an oxygen atom, or a linear or branched alkyl group having 1 to 5 carbon atoms which is unsubstituted or substituted with a halogen atom; wherein two adjacent groups among R 1 to R 5 may join together to form —O—CH 2 —O— or —O—(CH 2 ) 2 —O—;

R 6 to R 9 are each independently a hydrogen atom; a halogen atom; a hydroxyl group; a linear or branched alkoxy group having 1 to 5 carbon atoms; a linear or branched alkoxy group having 1 to 5 carbon atoms which is substituted with a group —C(O)A, wherein A is a saturated or unsaturated 5- or 6-membered ring which is unsubstituted or substituted with a linear or branched alkyl group having 1 to 5 carbon atoms and the ring may contain 1 or 2 atoms independently selected from a nitrogen atom, an oxygen atom and a sulfur atom; a linear or branched alkyl group having 1 to 5 carbon atoms which is unsubstituted or substituted with a halogen atom; or a group —NR 12 R 13 , wherein R 12 and R 13 are each independently a hydrogen atom, an oxygen atom, or a linear or branched alkyl group having 1 to 5 carbon atoms which is unsubstituted or substituted with a halogen atom; wherein two adjacent groups among R 6 to R 9 may join together to form —I—CH 2 —O— or —O—(CH 2 ) 2 —O—;

R 10 to R 11 are each independently a hydrogen atom; or a linear or branched alkyl group having 1 to 5 carbon atoms;

X is —CR 14 , wherein R 14 is a hydrogen atom, a halogen atom, a hydroxyl group, a linear or branched alkoxy group having 1 to 5 carbon atoms, or a linear or branched alkyl group having 1 to 5 carbon atoms which is unsubstituted or substituted with a halogen atom; an oxygen atom; a sulfur atom; a selenium atom; or a group —NR 15 , wherein R 15 is a hydrogen atom, a linear or branched alkyl group having 1 to 5 carbon atoms, or a linear or branched acyl group having 1 to 5 carbon atoms; and

n is an integer of 0 to 6;

or a salt thereof.

3. The method of claim 2 , wherein

R 1 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , and R 11 are a hydrogen atom;

R 2 and R 3 are each independently a methoxy group, an ethoxy group or a propoxy group;

R 7 is a hydrogen atom; a halogen atom; a hydroxyl group, a linear or branched alkoxy group having 1 to 5 carbon atoms; a linear or branched alkoxy group having 1 to 5 carbon atoms which is substituted with a group —C(O)A, wherein A is a saturated or unsaturated 5- or 6-membered ring which is unsubstituted or substituted with a linear or branched alkyl group having 1 to 5 carbon atoms and the ring may contain 1 or 2 atoms independently selected from a nitrogen atom, an oxygen atom and a sulfur atom; a linear or branched alkyl group having 1 to 5 carbon atoms which is unsubstituted or substituted with a halogen atom; or a group —NR 12 R 13 , wherein R 12 and R 13 are each independently a hydrogen atom, an oxygen atom, or a linear or branched alkyl group having 1 to 5 carbon atoms which is unsubstituted or substituted with a halogen atom;

X is a sulfur atom, and

n is an integer of 0 to 4.

4. The method of claim 3 , wherein R 7 is a halogen atom.

5. The method of claim 1 , wherein the WNT signaling inhibitor is a compound selected from the group consisting of:

or a salt thereof.

6. The method of claim 5 , wherein the WNT signaling inhibitor is KY02111, SO3031 (KY01-I), SO2031 (KY02-I) or SO3042 (KY03-I).

7. The method of claim 1 , wherein the medium of step (2) comprises two or more WNT signaling inhibitors, and wherein one of the two or more WNT signaling inhibitors is the compound of Formula (I) or a salt thereof as recited in any one of claims 2 , 3 - 4 , and 5 - 6 , and one or more of the two or more WNT signaling inhibitors are selected from the group consisting of IWP2, XAV939, and IWR1.

8. The method of claim 1 , wherein the WNT signaling activator is BIO or CHIR99021.

9. The method of claim 1 , wherein the PKC activator is PMA or prostratin.

10. The method of claim 1 , wherein the Src inhibitor is A419259 or SU6656.

11. The method of claim 1 , wherein the EGFR inhibitor is AG1478 or gefitinib.

12. The method of claim 1 , wherein

the WNT signaling activator is CHIR99021,

the PKC activator is PMA,

the WNT signaling inhibitor comprises a compound selected from KY02111, SO3031 (KY01-I), SO2031 (KY02-I), and SO3042 (Ky03-I), and XAV939,

the Src inhibitor is A419259, and

the EGFR inhibitor is AG1478.

13. The method of claim 1 , wherein the media of the steps (1) and (2) do not contain any protein or peptide component.

14. The method of claim 1 , wherein the culturing of the steps (1) and (2) is in suspension culture.

15. The method of claim 1 , wherein the culturing of the step (1) is for 1 to 3 days and the culturing of the step (2) is for 2 to 13 days.

16. The method of claim 1 , wherein the pluripotent stem cell is a monkey or human pluripotent stem cell.

17. The method of claim 1 , which is used to prepare a cardiomyocyte.

18. A kit for promoting cardiac differentiation comprising a WNT signaling activator, a PKC activator, a WNT signaling inhibitor, a Src inhibitor, and an EGFR inhibitor, wherein

the WNT signaling activator is CHIR99021,

the PKC activator is PMA,

the WNT signaling inhibitor comprises a compound selected from

the Src inhibitor is A419259, and

the EGFR inhibitor is AG1478.