Your browser doesn't support javascript.
loading
Cartilage oligomeric matrix protein is a novel notch ligand driving embryonic stem cell differentiation towards the smooth muscle lineage.
Ma, Baihui; Yao, Fang; Xie, Nan; Mao, Chenfeng; Liu, Fei; Gong, Ze; Zhao, Guizhen; Liu, Zhujiang; Cai, Zeyu; Yu, Fang; Dai, Rongbo; Chen, Zhongjiang; Wang, Li; Xu, Qingbo; Kong, Wei; Fu, Yi.
Afiliación
  • Ma B; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, PR China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, PR China.
  • Yao F; State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, PR China.
  • Xie N; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, PR China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, PR China.
  • Mao C; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, PR China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, PR China.
  • Liu F; State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, PR China.
  • Gong Z; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, PR China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, PR China.
  • Zhao G; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, PR China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, PR China.
  • Liu Z; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, PR China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, PR China.
  • Cai Z; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, PR China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, PR China.
  • Yu F; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, PR China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, PR China.
  • Dai R; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, PR China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, PR China.
  • Chen Z; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, PR China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, PR China.
  • Wang L; State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, PR China.
  • Xu Q; BHF Centre, School of Cardiovascular Medicine & Science, King's College London, London, United Kingdom. Electronic address: qingbo.xu@kcl.ac.uk.
  • Kong W; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, PR China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, PR China. Electronic address: kongw@bjmu.edu.cn.
  • Fu Y; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, PR China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, PR China. Electronic address: yi.fu@bjmu.edu.cn.
J Mol Cell Cardiol ; 121: 69-80, 2018 08.
Article en En | MEDLINE | ID: mdl-29981303
ABSTRACT
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.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cartílago / Diferenciación Celular / Receptor Notch1 / Proteína de la Matriz Oligomérica del Cartílago Límite: Animals / Humans Idioma: En Revista: J Mol Cell Cardiol Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cartílago / Diferenciación Celular / Receptor Notch1 / Proteína de la Matriz Oligomérica del Cartílago Límite: Animals / Humans Idioma: En Revista: J Mol Cell Cardiol Año: 2018 Tipo del documento: Article