Autophagy is involved in the differentiation of epicardial progenitor cells into vascular smooth muscle cells in mice

被引:3
作者
Liu, Yajie [1 ]
Liu, Bin [1 ]
Li, Yu [1 ]
Li, Yingrui [1 ]
Du, Jianlin [1 ]
Deng, Songbai [1 ]
Jing, Xiaodong [1 ]
She, Qiang [1 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 2, Dept Cardiol, Chongqing 400016, Peoples R China
基金
中国国家自然科学基金;
关键词
Autophagy; Epicardial progenitor cells; Smooth muscle cells; Differentiation; REGENERATION; SIGNALS;
D O I
10.1016/j.yexcr.2018.12.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Most coronary smooth muscle cells(CoSMCs) are differentiated from epicardial progenitor cells(EPCs), but the specific mechanism is not fully investigated. Previous studies have shown that autophagy plays an important role for smooth muscle cells(SMCs) differentiation, yet whether autophagy is involved in the differentiation of EPCs into CoSMCs remains unclear. In the present study, We first isolated and cultured EPCs and continuously cultured them for 72 h. Then the autophagy induction and inhibition experiment was established by using the autophagy inducer Rapamycin(RAPA) and the inhibitor 3-Methyladenine(3-MA). And further animal experiments were conducted to observe the effects of autophagy on the development of coronary arteries. Our data showed that autophagy occurred in the differentiation of EPCs into SMCs. Over activation of autophagy may lead to early transient differentiation of EPCs, enhanced migration ability and weakened systolic function, but overall, CoSMC development is still inhibited. However, inhibition of autophagy may delay the differentiation of EPCs, thus reducing the number of coronary arteries. Together, all these processes indicate that autophagy may regulate the differentiation of EPCs into CoSMCs by affecting the time point of differentiation, and appropriate autophagy intensity is required during the development of CoSMCs.
引用
收藏
页码:60 / 71
页数:12
相关论文
共 33 条
[1]   Epigenetic Control of Smooth Muscle Cell Differentiation and Phenotypic Switching in Vascular Development and Disease [J].
Alexander, Matthew R. ;
Owens, Gary K. .
ANNUAL REVIEW OF PHYSIOLOGY, VOL 74, 2012, 74 :13-40
[2]  
BIEDERBICK A, 1995, EUR J CELL BIOL, V66, P3
[3]   A myocardial lineage derives from Tbx18 epicardial cells [J].
Cai, Chen-Leng ;
Martin, Jody C. ;
Sun, Yunfu ;
Cui, Li ;
Wang, Lianchun ;
Ouyang, Kunfu ;
Yang, Lei ;
Bu, Lei ;
Liang, Xingqun ;
Zhang, Xiaoxue ;
Stallcup, William B. ;
Denton, Christopher P. ;
McCulloch, Andrew ;
Chen, Ju ;
Evans, Sylvia M. .
NATURE, 2008, 454 (7200) :104-U4
[4]   Regulation of autophagy and apoptosis in response to ox-LDL in vascular smooth muscle cells, and the modulatory effects of the microRNA hsa-let-7g [J].
Ding, Zufeng ;
Wang, Xianwei ;
Schnackenberg, Laura ;
Khaidakov, Magomed ;
Liu, Shijie ;
Singla, Sandeep ;
Dai, Yao ;
Mehta, Jawahar L. .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2013, 168 (02) :1378-1385
[5]   Notch Signaling Regulates Smooth Muscle Differentiation of Epicardium-Derived Cells [J].
Grieskamp, Thomas ;
Rudat, Carsten ;
Luedtke, Timo H. -W. ;
Norden, Julia ;
Kispert, Andreas .
CIRCULATION RESEARCH, 2011, 108 (07) :813-U108
[6]   FIP200, a ULK-interacting protein, is required for autophagosome formation in mammalian cells [J].
Hara, Taichi ;
Takamura, Akito ;
Kishi, Chieko ;
Iemura, Shun-ichiro ;
Natsume, Tohru ;
Guan, Jun-Lin ;
Mizushima, Noboru .
JOURNAL OF CELL BIOLOGY, 2008, 181 (03) :497-510
[7]  
Ikeda N, 2017, BIOMED RES-TOKYO, V38, P228
[8]   Complex pattern of interaction between in utero hypoxia-ischemia and intra-amniotic inflammation disrupts brain development and motor function [J].
Jantzie, Lauren L. ;
Corbett, Christopher J. ;
Berglass, Jacqueline ;
Firl, Daniel J. ;
Flores, Julian ;
Mannix, Rebekah ;
Robinson, Shenandoah .
JOURNAL OF NEUROINFLAMMATION, 2014, 11
[9]   Autophagy of vascular smooth muscle cells in atherosclerotic lesions [J].
Jia, Guanghong ;
Cheng, Gang ;
Agrawal, Devendra K. .
AUTOPHAGY, 2007, 3 (01) :63-64
[10]   Hypoxia induced the differentiation of Tbx18-positive epicardial cells to CoSMCs [J].
Jing, Xiaodong ;
Gao, Yulin ;
Xiao, Songlin ;
Qin, Qin ;
Wei, Xiaoming ;
Yan, Yuling ;
Wu, Ling ;
Deng, Songbai ;
Du, Jianlin ;
Liu, Yajie ;
She, Qiang .
SCIENTIFIC REPORTS, 2016, 6