期刊文献+

线粒体融合蛋白2在心血管疾病中的研究现状 被引量:4

Mitofusin-2 in cardiac diseases
下载PDF
导出
摘要 线粒体是一个处于不断地融合与分裂过程中的动态细胞器。线粒体融合蛋白2(Mfn2)作为广泛分布于线粒体外膜和线粒体结合内质网膜上具有多重功能的蛋白,参与维持正常细胞功能。除了参与线粒体融合外,Mfn2还能够调节线粒体代谢、促进损伤线粒体的自噬、增强线粒体与内质网交流、维持内质网功能及通过调控线粒体外膜通透性和渗透性钙转运孔道的启闭参与细胞死亡过程等。另外,Mfn2基因还可通过调控Ras-Raf-ERK/MAPK和Ras-PI3K-Akt信号通路分别参与调控血管平滑肌细胞的增殖和凋亡过程。Mfn2的这一系列重要的生物学功能有助于其参与高血压、肺动脉高压、动脉粥样硬化、急性缺血/再灌损伤、扩张性心肌病、心肌肥大、心衰和肥胖糖尿病等多种心血管疾病的发生发展过程。研究Mfn2与心血管疾病的相关性也许能为临床提供一个心血管疾病潜在治疗的靶点。因此,本文将综述Mfn2在心血管疾病相关研究中的现状。 Mitochondria are highly dynamic organelles with constant fusion and fission. Mitofusin-2( Mfn2) is widely distributed on the outer membrane of mitochondria and mitochondria-associated endoplasmic reticulum membrane( MAM) with multiple functions to sustain normal cell function. In addition to promoting mitochondrial fusion,Mfn2 also participates in injured mitochondria mitophagy,tethers endoplasmic reticulum( ER) to mitochondria,sustains ER structure and functions and plays critical roles in several cell death pathways( including apoptosis and necrotic cell death) by mediating mitochondrial outer membrane permeabilization and facilitating opening of the mitochondrial permeability pore( m PTP)during death. Moreover,Mfn2 gene regulates vascular smooth muscle cell( VSMC) proliferation via Ras-Raf-ERK / MAPK and Ras-PI3K-Akt pathways. Mfn2 is associated with cardiac diseases including hypertension,pulmonary artery hypertension,atherosclerosis,dilated cardiomyopathy,acute ischemic reperfusion injury,cardiac hypertrophy,heart failure and major metabolic disturbance such as diabetes and obesity. Exploration of the relationships between Mfn2 and cardiac diseases may provide therapeutic potentials for cardiac diseases.
出处 《心脏杂志》 CAS 2015年第2期224-228,共5页 Chinese Heart Journal
基金 国家杰出青年科学基金项目资助(81225001)
关键词 线粒体融合蛋白2 内质网 线粒体自噬 心血管疾病 mitofusin-2 endoplasmic reticulum mitophagy cardiac diseases
  • 相关文献

参考文献22

  • 1Escobar-Henriques M, Anton F. Mechanistic perspective of mito- chondrial fusion : tubulation vs. fragmentation[ J]. Biochim Biophys Acta, 2013, 1833(1) :162 -175. 被引量:1
  • 2Hall AR, Burke N, Dongworth RK, et al. Mitochondrial fusion and fission proteins : novel therapeutic targets for combating cardiovascular disease [ J ]. Br J Pharmacol, 2014, 171 ( 8 ) : 1890 - 1906. 被引量:1
  • 3Hoppins S, Edlich F, Cleland MM, et al. The soluble form of Bax regulates mitochondrial fusion via MFN2 homotypie complexes [ J ]. Mol Cell, 2011,41 (2) :150-160. 被引量:1
  • 4Dorn IW. Mitochondrial dynamism and cardiac fate [ J ]. Circ J, 2013, 77(6) :1370 -1379. 被引量:1
  • 5Mutioz JP, Zorzano A. Mfn2 modulates the unfolded protein response[J]. Cell Cycle, 2014, 13(4) :491 -492. 被引量:1
  • 6Chen Y, Dorn GW. PINKl-phosphorylated mitofusin 2 is a Parkinreceptor for culling damaged mitochandria [ J ]. Science, 2013, 5g0 (6131) :471 -475. 被引量:1
  • 7Drew BG, Ribas V, Le JA, et al. HSP72 is a mitochondrial stress sensor critical for Parkin action, oxidative metabolism, and insulin sensitivity in skeletal muscle[J]. D/abetes, 2014, 63(5):1458-15(15. 被引量:1
  • 8Zhao T, Huang X, Han L, et al. Central role of mitofusin 2 in auto- phagosome-lysosome fusion in cardiomyocytes [ J ]. J Biol Chem, 2012, 287 (28) :23615 - 23625. 被引量:1
  • 9de Bfito OM, Scorrano L. Mitofusin 2 tethers endoplasmic reticulum to mitochondria[ J]. Nature, 2008, 456 (7222) :605 - 610. 被引量:1
  • 10Chen Y, Csordds G, Jowdy C, et al. Mitofusin 2-containing mito- chondrial-reticular microdomains direct rapid cardiomyocyte bioener- getic responses via interorganelle Ca(2 + ) crosstalk [ J ]. Circ Res, 2012, 111(7) :863 -875. 被引量:1

同被引文献31

引证文献4

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部