Mitochondrial Dynamics in Drug-Induced Liver Injury

被引:26
作者
Ramachandran, Anup [1 ]
Umbaugh, David S. [1 ]
Jaeschke, Hartmut [1 ]
机构
[1] Univ Kansas, Med Ctr, Dept Pharmacol Toxicol & Therapeut, Kansas City, KS 66160 USA
来源
LIVERS | 2021年 / 1卷 / 03期
基金
美国国家卫生研究院;
关键词
drug-induced liver injury; acetaminophen; mitochondrial dynamics; fusion; fission; INDUCED HEPATOTOXICITY; REPERFUSION INJURY; PHOSPHATIDIC-ACID; BIOGENESIS; FISSION; FUSION; DRP1; MECHANISMS; INHIBITION; MITOPHAGY;
D O I
10.3390/livers1030010
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Mitochondria have been studied for decades from the standpoint of metabolism and ATP generation. However, in recent years mitochondrial dynamics and its influence on bioenergetics and cellular homeostasis is also being appreciated. Mitochondria undergo regular cycles of fusion and fission regulated by various cues including cellular energy requirements and pathophysiological stimuli, and the network of critical proteins and membrane lipids involved in mitochondrial dynamics is being revealed. Hepatocytes are highly metabolic cells which have abundant mitochondria suggesting a biologically relevant role for mitochondrial dynamics in hepatocyte injury and recovery. Here we review information on molecular mediators of mitochondrial dynamics and their alteration in drug-induced liver injury. Based on current information, it is evident that changes in mitochondrial fusion and fission are hallmarks of liver pathophysiology ranging from acetaminophen-induced or cholestatic liver injury to chronic liver diseases. These alterations in mitochondrial dynamics influence multiple related mitochondrial responses such as mitophagy and mitochondrial biogenesis, which are important adaptive responses facilitating liver recovery in several contexts, including drug-induced liver injury. The current focus on characterization of molecular mechanisms of mitochondrial dynamics is of immense relevance to liver pathophysiology and have the potential to provide significant insight into mechanisms of liver recovery and regeneration after injury.
引用
收藏
页码:102 / 115
页数:14
相关论文
共 101 条
[1]   Mitochondrial dynamics regulate myocardial contractility and vice versa [J].
Abdelwahid, Eltyeb .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2017, 247 :35-35
[2]   Drug induced liver injury is associated with high mortality-A study from a tertiary care hospital in Pakistan [J].
Abid, Adeel ;
Subhani, Faryal ;
Kayani, Farhana ;
Awan, Safia ;
Abid, Shahab .
PLOS ONE, 2020, 15 (04)
[3]   Coincident Phosphatidic Acid Interaction Restrains Drp1 in Mitochondrial Division [J].
Adachi, Yoshihiro ;
Itoh, Kie ;
Yamada, Tatsuya ;
Cerveny, Kara L. ;
Suzuki, Takamichi L. ;
Macdonald, Patrick ;
Frohman, Michael A. ;
Ramachandran, Rajesh ;
Iijima, Miho ;
Sesaki, Hiromi .
MOLECULAR CELL, 2016, 63 (06) :1034-1043
[4]   Mitochondrial DNA Transcription and Its Regulation: An Evolutionary Perspective [J].
Barshad, Gilad ;
Marom, Shani ;
Cohen, Tal ;
Mishmar, Dan .
TRENDS IN GENETICS, 2018, 34 (09) :682-692
[5]   Acute Liver Failure [J].
Bernal, William ;
Wendon, Julia .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 369 (26) :2525-2534
[6]   Irisin alleviates liver ischemia-reperfusion injury by inhibiting excessive mitochondrial fission, promoting mitochondrial biogenesis and decreasing oxidative stress [J].
Bi, Jianbin ;
Zhang, Jia ;
Ren, Yifan ;
Du, Zhaoqing ;
Li, Qingshan ;
Wang, Yue ;
Wei, Shasha ;
Yang, Lifei ;
Zhang, Jingyao ;
Liu, Chang ;
Lv, Yi ;
Wu, Rongqian .
REDOX BIOLOGY, 2019, 20 :296-306
[7]   Mitochondrial abnonnalities - A link to idiosyncratic drug hepatotoxicity? [J].
Boelsterli, Urs A. ;
Lim, Priscilla L. K. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2007, 220 (01) :92-107
[8]   Mitochondrial fission facilitates the selective mitophagy of protein aggregates [J].
Burman, Jonathon L. ;
Pickles, Sarah ;
Wang, Chunxin ;
Sekine, Shiori ;
Vargas, Jose Norberto S. ;
Zhang, Zhe ;
Youle, Alice M. ;
Nezich, Catherine L. ;
Wu, Xufeng ;
Hammer, John A. ;
Youle, Richard J. .
JOURNAL OF CELL BIOLOGY, 2017, 216 (10) :3231-3247
[9]   Experimental sepsis-induced mitochondrial biogenesis is dependent on autophagy, TLR4, and TLR9 signaling in liver [J].
Carchman, Evie H. ;
Whelan, Sean ;
Loughran, Patricia ;
Mollen, Kevin ;
Stratamirovic, Sladjana ;
Shiva, Sruti ;
Rosengart, Matthew R. ;
Zuckerbraun, Brian S. .
FASEB JOURNAL, 2013, 27 (12) :4703-4711
[10]   INF2-mediated actin polymerization at the ER stimulates mitochondrial calcium uptake, inner membrane constriction, and division [J].
Chakrabarti, Rajarshi ;
Ji, Wei-Ke ;
Stan, Radu V. ;
de Juan-Sanz, Jaime ;
Ryan, Timothy A. ;
Higgs, Henry N. .
JOURNAL OF CELL BIOLOGY, 2018, 217 (01) :251-268