Cartilage oligomeric matrix protein is a novel notch ligand driving embryonic stem cell differentiation towards the smooth muscle lineage

被引:10
作者
Ma, Baihui [1 ,5 ]
Yao, Fang [2 ,3 ]
Xie, Nan [1 ,5 ]
Mao, Chenfeng [1 ,5 ]
Liu, Fei [2 ,3 ]
Gong, Ze [1 ,5 ]
Zhao, Guizhen [1 ,5 ]
Liu, Zhujiang [1 ,5 ]
Cai, Zeyu [1 ,5 ]
Yu, Fang [1 ,5 ]
Dai, Rongbo [1 ,5 ]
Chen, Zhongjiang [1 ,5 ]
Wang, Li [2 ,3 ]
Xu, Qingbo [4 ]
Kong, Wei [1 ,5 ]
Fu, Yi [1 ,5 ]
机构
[1] Peking Univ, Sch Basic Med Sci, Dept Physiol & Pathophysiol, Beijing, Peoples R China
[2] Chinese Acad Med Sci, Natl Ctr Cardiovasc Dis, Fuwai Hosp, State Key Lab Cardiovasc Dis, Beijing, Peoples R China
[3] Peking Union Med Coll, Beijing, Peoples R China
[4] Kings Coll London, Sch Cardiovasc Med & Sci, BHF Ctr, 125 Coldharbour Lane, London SE5 9NU, England
[5] Minist Educ, Key Lab Mol Cardiovasc Sci, Beijing, Peoples R China
基金
国家重点研发计划;
关键词
Embryonic stem cells; Vascular smooth muscle cells; COMP; Notch signaling; EXTRACELLULAR-MATRIX; SIGNALING PATHWAY; CONTRACTILE PHENOTYPE; METALLOPROTEINASE; CALCIFICATION; MAINTENANCE; DERIVATION; ADAMTS-7; ARTERIES; DISEASE;
D O I
10.1016/j.yjmcc.2018.07.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cartilage oligomeric matrix protein (COMP), a protective component of vascular extracellular matrix (ECM), maintains the homeostasis of mature vascular smooth muscle cells (VSMCs). However, whether COMP modulates the differentiation of stem cells towards the smooth muscle lineage is still elusive. Firstly, purified mouse COMP directly induced mouse embryonic stem cell (ESC) differentiation into VSMCs both in vitro and in vivo, while the silencing of endogenous COMP markedly inhibited ESC-VSMC differentiation. RNA-Sequencing revealed that Notch signaling was significantly activated by COMP during ESC-VSMC differentiation, whereas the inhibition of Notch signaling attenuated COMP-directed ESC-VSMC differentiation. Furthermore, COMP deficiency inhibited Notch activation and VSMC differentiation in mice. Through silencing distinct Notch receptors, we identified that Notch1 mainly mediated COMP-initiated ESC-VSMC differentiation. Mechanistically, COMP N-terminus directly interacted with the EGF11-12 domain of Notch1 and activated Notch1 signaling, as evidenced by co-immunoprecipitation and mammalian two-hybrid assay. In conclusion, COMP served as a potential ligand of Notch1, thereby driving ESC-VSMC differentiation.
引用
收藏
页码:69 / 80
页数:12
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