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线粒体与肝细胞损伤的关系

魏海梁 司明明 郭辉 李京涛 李倩 闫曙光 鞠迪

引用本文:
Citation:

线粒体与肝细胞损伤的关系

DOI: 10.3969/j.issn.1001-5256.2020.03.048
基金项目: 

国家自然科学基金项目(81603612,81904192); 陕西省科技厅课题(2012SF2-11,2014K11-02-04-06,2016SF-234); 陕西省中医药管理局课题(15-JC009); 陕西中医药大学学科创新团队建设项目(2019-YL05); 

详细信息
  • 中图分类号: R575

Association between mitochondria and hepatocellular injury

Research funding: 

 

  • 摘要: 在肝脏组织中,线粒体不但为肝细胞的物质代谢提供了能量,同时还广泛参与了肝细胞损伤甚至凋亡的过程,在与肝细胞损伤、凋亡密切相关的肝炎、肝纤维化、肝癌癌前病变及肝癌的病理过程中也发挥了重要的作用。从线粒体膜通透性的改变在肝细胞损伤中的重要作用、ATP合成障碍及消耗加速肝细胞损伤以及肝细胞线粒体Ca2+稳态异常与肝细胞损伤关系等方面阐述了线粒体与肝细胞损伤之间的关系,以期以线粒体为靶点,为防治肝细胞损伤引起的慢性肝脏疾病提供理论依据。

     

  • [1] MARUF AA,O'BRIEN PJ,NASERZADEH P,et al. Methotrexate induced mitochondrial injury and cytochrome c release in rat liver hepatocytes[J]. Drug Chem Toxicol,2017,41(1):1-11.
    [2] MNATSAKANYAN N,BEUTNER G,PORTER GA,et al. Physiological roles of the mitochondrial permeability transition pore[J]. J Bioenerg Biomembr,2017,49(1):13-25.
    [3] BEUTNER G,ALAVIAN K N,JONAS EA,et al. The mitochondrial permeability transition pore and ATP synthase[J]. Handb Exp Pharmacol,2017,240:21-46.
    [4]ŠILEIKYTE J,FORTE M. The mitochondrial permeability transition in mitochondrial disorders[J]. Oxid Med Cell Longev,2019,2019:3403075.
    [5] HE J,FORD H C,CARROLL J,et al. Persistence of the mitochondrial permeability transition in the absence of subunit c of human ATP synthase[J]. Proc Natl Acad Sci U S A,2017,114(13):3409-3414.
    [6] BERNARDI P,RASOLA A,Forte M,et al. The mitochondrial permeability transition pore:Channel formation by F-ATP synthase,integration in signal transduction,and role in pathophysiology[J]. Physiological Reviews,2015,95(4):1111-1155.
    [7] RICCHELLI F,ŠILEIKYTE J,BERNARDI P. Shedding light on the mitochondrial permeability transition[J]. Biochimica Et Biophysica Acta,2011,1807(5):482-490.
    [8] DAS N,MANDALA A,NAAZ S,et al. Melatonin protects against lipid-induced mitochondrial dysfunction in hepatocytes and inhibits stellate cell activation during hepatic fibrosis in mice[J]. J Pineal Res,2017,62(4):e12404.
    [9] AKBARI G. Role of Zinc supplementation on ischemia/reperfusion injury in various organs[J]. Biol Trace Elem Res,2019.[Epub ahead of print]
    [10] MARD SA,AKBARI G,DIANAT M,et al. Protective effects of crocin and zinc sulfate on hepatic ischemia-reperfusion injury in rats:A comparative experimental model study[J]. Biomed Pharmacother,2017,96:48-55.
    [11] NARYZHNAYA NV,MASLOV LN,OELTGEN PR. Pharmacology of mitochondrial permeability transition pore inhibitors[J].Drug Dev Res,2019,80(8):1013-1030.
    [12] PANEL M,RUIZ I,BRILLET R,et al. Small-molecule inhibitors of cyclophilins block opening of the mitochondrial permeability transition pore and protect mice from hepatic ischemia/reperfusion injury[J]. Gastroenterology,2019,157(5):1368-1382.
    [13] SUN Y,SUKUMARAN P,SELVARAJ S,et al. TRPM2 promotes neurotoxin MPP+/MPTP-induced cell death[J]. Mol Neurobiol,2018,55(1):409-420.
    [14] FRIEDMAN JR,NUNNARI J. Mitochondrial form and function[J]. Nature,2014,505(7483):335-343.
    [15] CHEN X,YANG S,PAN Y,et al. Mitochondrial pathway-mediated apoptosis is associated with erlotinib-induced cytotoxicity in hepatic cells[J]. Oncology Letters,2018,15(1):783-788.
    [16] DAVE M,ATTUR M,PALMER G,et al. The antioxidant resveratrol protects against chondrocyte apoptosis via effects on mitochondrial polarization and ATP production[J]. Arthritis Rheum,2014,58(9):2786-2797.
    [17] FLORES-TORO JA,GO KL,LEEUWENBURGH C,et al. Autophagy in the liver:Cell's cannibalism and beyond[J]. Arch Pharm Res,2016,39(8):1050-1061.
    [18] BURKE PJ. Mitochondria,bioenergetics and apoptosis in cancer[J]. Trends Cancer,2017,3(12):857-870.
    [19] ZOU LY,ZHENG BY,FANG XF,et al. HBx co-localizes with COXIII in HL-7702 cells to upregulate mitochondrial function and ROS generation[J]. Oncology Reports,2015,33(5):2461-2467.
    [20] NASSIR F,IBDAH JA. Role of mitochondria in alcoholic liver disease[J]. World J Gastroenterol,2014,20(9):2136-2142.
    [21] LI J,WU DD,ZHANG JX,et al. Mitochondrial pathway mediated by reactive oxygen species involvement inα-hederininduced apoptosis in hepatocellular carcinoma cells[J].World J Gastroenterol,2018,24(17):1901-1910.
    [22] KRABBENDAM IE,HONRATH B,CULMSEE C,et al. Mitochondrial Ca2+-activated K+channels and their role in cell life and death pathways[J]. Cell Calcium,2018,69:101-111.
    [23] NURIA OV,SIMONA H,VORRINK SU,et al. Calcium signaling in liver injury and regeneration[J]. Front Med(Lausanne),2018,5:192.
    [24] ANTONY AN,PAILLARD M,MOFFAT C,et al. MICU1 regulation of mitochondrial Ca2+uptake dictates survival and tissue regeneration[J]. Nature Communications,2016,7:10955.
    [25] GUERRA MT,FONSECA EA,MELO FM,et al. Mitochondrial calcium regulates rat liver regeneration through the modulation of apoptosis[J]. Hepatology,2011,54(1):296-306.
    [26] CSORDÁS G,GOLENÁR T,SEIFERT EL,et al. MICU1 controls both the threshold and cooperative activation of the mitochondrial Ca2+uniporter[J]. Cell Metab,2013,17(6):976-987.
    [27] EMBADE N,MILLET O. Molecular determinants of chronic liver disease as studied by nmr-metabolomics[J]. Curr Top Med Chem,2017,17(24):2752.
    [28] SRINIVASAN S,GUHA M,KASHINA A,et al. Mitochondrial dysfunction and mitochondrial dynamics-The cancer connection[J]. Biochim Biophys Acta Bioenerg,2017,1858(8):602-614.
    [29] IOMMARINI L,GHELLI A,GASPARRE G,et al. Mitochondrial metabolism and energy sensing in tumor progression[J]. Biochim Biophys Acta Bioenerg,2017,1858(8):582-590.
    [30] MANSOURI A,GATTOLLIAT CH,ASSELAH T. Mitochondrial dysfunction and signaling in chronic liver diseases[J]. Gastroenterology,2018,155(3):629-647.
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  • 收稿日期:  2019-11-29
  • 出版日期:  2020-03-20
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