| Literature DB >> 31825822 |
Yang Yang1, Zhili Ren1, Faxiang Xu1, Ya Meng1, Yumeng Zhang1, Nana Ai1, Yan Long2, Hio Ian Fok3, Chunhao Deng1, Xianyang Zhao4, Liancheng Huang5, Qi Zhao1, Jiaxian Wang6, Weiwei Liu3, Wei Ge1, Guokai Chen7.
Abstract
During embryogenesis, various cell types emerge simultaneously from their common progenitors under the influence of intrinsic signals. Human embryonic stem cells can differentiate to diverse cell types of three embryonic lineages, making them an excellent system for understanding the regulatory mechanism that maintains the balance of different cell types in embryogenesis. In this report, we demonstrate that insulin-like growth factor (IGF) proteins are endogenously expressed during differentiation, and their temporal expression contributes to the cell fate diversity in mesoderm differentiation. Small molecule LY294002 inhibits the IGF pathway to promote cardiomyocyte differentiation while suppressing epicardial and noncardiac cell fates. LY294002-induced cardiomyocytes demonstrate characteristic cardiomyocyte features and provide insights into the molecular mechanisms underlying cardiac differentiation. We further show that LY294002 induces cardiomyocytes through CK2 pathway inhibition. This study elucidates the crucial roles of endogenous IGF in mesoderm differentiation and shows that the inhibition of the IGF pathway is an effective approach for generating cardiomyocytes.Entities:
Keywords: IGF; PI3K; WNT; cardiomyocyte; casein kinase II; heterogeneity; human embryonic stem cells; insulin; mesoderm; temporal regulation
Year: 2019 PMID: 31825822 DOI: 10.1016/j.celrep.2019.11.047
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423