Mitogen-activated protein kinase p38 modulates pacemaker ion channels differentiation in P19-derived pluripotent cells

The journal of physiological sciences

article

Mingqi Zheng¹  Lin Kang¹  Tomoko Uchino¹  Gang Liu²  Yan Wang¹  Katsushige Ono¹ 

[1] Department of Pathophysiology, Oita University School of Medicine;Department of Cardiovascular Medicine, Hebei Medical University;Department of Anatomy, Hebei Medical University;Department of Anesthesiology, Oita University School of Medicine

关键词: Csx/Nkx2.5;    GATA4;    MEF2C;    p38MAP kinase;    Cardiogenesis;    P19CL6;   

DOI  :  10.1186/s12576-020-00766-x

来源: Springer

【 摘 要 】

Signal regulators during early cardiogenetic differentiation for the cellular automaticity are largely unknown. Our investigations were designed to clarify the role of transcription factors and their modulators in P19-derived cardiomyocytes to the expression of cardiac pacemaker ion channels. Transcription factors Csx/Nkx2.5 and GATA4 but not MEF2C were markedly inhibited by p38 MAP kinase inhibition in a distinct manner; expression but not phosphorylation of GATA4 was reduced by inhibition of p38 MAP kinase actions. In the presence of an ERK1/2,5 inhibitor PD98059 or a JNK MAP kinase inhibitor SP600125, P19 cells successfully differentiated into cardiomyocytes displaying spontaneous beatings with expression of three types of pacemaker ion channels. We demonstrate that acquisition of cellular automaticity and the expression of pacemaker ion channels are regulated by the transcription factors, Csx/Nkx2.5 and GATA4, through intracellular signals including p38 MAP kinase in the process of P19-derived pluripotent cells differentiation into cardiomyocytes.

【 授权许可】

Unknown