期刊文献+

线粒体质量控制新途径:线粒体衍生囊泡 被引量:1

A new pathway for mitochondrial quality control:mitochondrial-derived vesicle
下载PDF
导出
摘要 线粒体是真核细胞中非常复杂的双膜细胞器。在生理状态下,线粒体再生和降解是平衡的;细胞器中的蛋白质、脂质和DNA等组分受到损伤时,通过分裂、融合、自噬等途径维持线粒体稳态,以保持线粒体结构和功能的完整,这一过程通常称为"线粒体质量控制"。线粒体衍生囊泡(MDV)是新近发现的线粒体质量控制途径,在细胞应激早期有助于维持线粒体功能稳定,并在线粒体氧化应激中发挥重要作用。我们拟综述MDV的发现、转运途径、货物的选择以及对细胞的生理影响等。 Mitochondria are very complex dual membrane organelles in eukaryotic cells.Under physiological conditions,the regeneration and degradation of mitochondria are balanced.When the components of the proteins,lipids and DNA in the organelles are damaged,the steady state of the mitochondria is maintained by means of division,fusion,autophagy and the like,so as to maintain the integrity of the mitochondrial structure and function,which is commonly referred to as a"mitochondrial mass control".Mitochondrial-derived vesicle(MDV)is a newly discovered pathway of mitochondrial quality control,which plays an important role in the early stage of cell stress and helps maintain the stability of mitochondrial function.In this paper,the discovery of MDV,the transport pathway,the choice of goods and the physiological effects on cells are reviewed.
作者 官伟康 吕静 杨朝鲜 GUAN Wei-kang;Lü Jing;YANG Chao-xian(Center for Basic Medical Research,Southwest Medical University;Department of Anatomy,Southwest Medical University,Sichuang Luzhou 646000)
出处 《解剖学报》 CAS CSCD 北大核心 2021年第1期152-156,共5页 Acta Anatomica Sinica
基金 泸州市-西南医大战略合作项目(2018LZXNYDZK35) 四川省教育厅自然科学重点项目(18ZA0516)。
关键词 线粒体 线粒体质量控制 线粒体衍生囊泡 Mitochondria Mitochondrial quality control Mitochondrial-derived vesicle
  • 相关文献

参考文献2

二级参考文献47

  • 1张朝佑.人体解剖学[M].第3版.北京:人民卫生出版,2009:1914.
  • 2Braak H, Del Tredici K, Rub U, et al. Staging of brain pathology related to sporadic Parkinson' s disease [ J l. Neurobiol Aging, 2003, 24 (2) : 197-211.
  • 3Zarow C, Lyness SA, Mortimer JA, et al. Neuronal loss is greater in the locus coeruleus than nucleus basalis and substantia nigra in Alzheimer and Parkinson diseases [ J ]. Arch Neurol, 2003, 60 (3) :337-341.
  • 4Dickson DW. Parkinson ' s disease and parkinsonism : neuropathology [ J]. Cold Spring Harb Perspect Med, 2012, 2 (8) : a009258.
  • 5Del Tredici K, Rub U, De Vos RA, et al. Where does parkinson disease pathology begin in the brain [ J ] ? J Neuropathol Exp Neurol, 2002, 61 ( 5 ) :413-426.
  • 6Marien MR, Colpaert FC, Rosenquist AC. Noradrenergic mechanisms in neurodegenerative diseases: a theory [ J]. Brain Res Brain Res Rev, 2004, 45(1 ):38-78.
  • 7German DC, Manaye KF, White CL 3rd, et al. Disease-specific patterns of locus eoeruleus cell loss [ J]. Ann Neural, 1992, 32 (5) :667-676.
  • 8Patt S, Gerhard L. A Golgi study of human locus coeruleus in normal brains and in Parkinson' s disease [ J ]. Neuropathol Appl Neurobiol, 1993, 19(6) :519-523.
  • 9Gesi M, Soldani P, Giorgi FS, et al. The role of the locus eoeruleus in the development of Parkinson' s disease [ J]. Neurosei Biobehav Rev, 2000, 24(6):655-668.
  • 10Baloyannis SJ, Costa V, Baloyannis IS. Morphological alterations of the synapses in the locus eoeruleus in Parkinson' s disease [ J]. J Neural Sci, 2006, 248(1-2) :35-41.

共引文献10

引证文献1

二级引证文献1

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