安宇轩.线粒体调控细胞命运途径的研究进展.[J].中南医学科学杂志.,2024,(3):496-500.
线粒体调控细胞命运途径的研究进展
Research progress on mitochondria regulation of cell fate pathways
投稿时间:2023-11-02  修订日期:2024-04-02
DOI:10.15972/j.cnki.43-1509/r.2024.03.047
中文关键词:  线粒体  调控  细胞命运 [
英文关键词:mitochondria  regulation  cell fate
基金项目:南华大学大学生创新项目(202110555091)
作者单位E-mail
安宇轩 南华大学衡阳医学院,湖南衡阳421001 e-mail为1659003526@qq.com 
摘要点击次数: 136
全文下载次数: 257
中文摘要:
      线粒体是动态且高度可塑的细胞器,是细胞的能量工厂,具有调控细胞内能量生成、代谢以及信号转导的作用。研究表明,线粒体调控细胞增殖、凋亡、衰老、分化、细胞周期等与细胞命运密切相关的生物学过程,表明线粒体在调控细胞命运过程中发挥着重要的生物学作用。本文综述了线粒体能量代谢、线粒体蛋白、活性氧、线粒体DNA、线粒体动力学调控细胞命运的机制,以期为细胞命运的调控提供新的策略和靶点。
英文摘要:
      Mitochondria are dynamic and highly plastic organelles, and are the energy factories of cells, playing a role in regulating intracellular energy generation, metabolism, and signal transduction. Researches have shown that mitochondria regulate many biological processes, such as proliferation, apoptosis, aging, differentiation, and cell cycle, indicating that mitochondria play an important biological role in regulating cell fate. This article reviews the mechanisms by which mitochondrial energy metabolism, mitochondrial proteins, reactive oxygen species, mitochondrial DNA, and mitochondrial dynamics regulate cell fate, in order to provide new strategies and targets for the regulation of cell fate.
查看全文  查看/发表评论  下载PDF阅读器
关闭
function PdfOpen(url){ var win="toolbar=no,location=no,directories=no,status=yes,menubar=yes,scrollbars=yes,resizable=yes"; window.open(url,"",win); } function openWin(url,w,h){ var win="toolbar=no,location=no,directories=no,status=no,menubar=no,scrollbars=yes,resizable=no,width=" + w + ",height=" + h; controlWindow=window.open(url,"",win); } &et=FC9DA7BF2F842A3BAE24B54F70914FE67C25643EDD2D5783B8F23EC1A3319B14E472C403C5DB9E68C1A52CAE4979B36DC751F82521C0D74F7CDEB36A56F9283D75252EDFF2B46998&pcid=A9DB1C13C87CE289EA38239A9433C9DC&cid=BB33F1C95224820A&jid=6A20DF2A798996E24F064D5ECF83A153&yid=B80136CCD8DCBAA1&aid=&vid=&iid=38B194292C032A66&sid=C4490A71BEB872FA&eid=8566B4AE2A8832E3&fileno=20240347&flag=1&is_more=0">