Literature DB >> 16286505

Death by association: BH3 domain-only proteins and liver injury.

E S Baskin-Bey1, G J Gores.   

Abstract

Apoptosis, a prominent form of cell death, is a prime feature of many acute and chronic liver diseases. Apoptosis requires mitochondrial dysfunction, which is regulated by proteins of the Bcl-2 family. Whether or not a cell should live or die is controlled by the interaction of multidomain Bcl-2 proteins with proapoptotic BH3 domain-only proteins of this family. Current models suggest multidomain, antiapoptotic Bcl-2 proteins prevent mitochondrial dysfunction by sequestering and/or preventing activation of its proapoptotic relatives. BH3-only proteins initiate cell death by neutralizing and or ligating multidomain prosurvival Bcl-2 proteins. Thus BH3 domain-only proteins are paramount in the apoptotic process as exemplified by the role of the BH3 domain-only protein Bid in liver injury. In this concise review, we will focus on how these BH3 domain-only proteins are regulated in the cell, their association with the Bcl-2 family of proteins, and finally, current information regarding their involvement in liver cell apoptosis and injury.

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Year:  2005        PMID: 16286505     DOI: 10.1152/ajpgi.00371.2005

Source DB:  PubMed          Journal:  Am J Physiol Gastrointest Liver Physiol        ISSN: 0193-1857            Impact factor:   4.052


  6 in total

1.  Differential effects of JNK1 and JNK2 inhibition on murine steatohepatitis and insulin resistance.

Authors:  Rajat Singh; Yongjun Wang; Youqing Xiang; Kathryn E Tanaka; William A Gaarde; Mark J Czaja
Journal:  Hepatology       Date:  2009-01       Impact factor: 17.425

2.  Deficiency of Bid protein reduces sepsis-induced apoptosis and inflammation, while improving septic survival.

Authors:  Chun-Shiang Chung; Fabienne Venet; Yaping Chen; Leslie N Jones; Douglas C Wilson; Carol A Ayala; Alfred Ayala
Journal:  Shock       Date:  2010-08       Impact factor: 3.454

Review 3.  Apoptosis in nonalcoholic fatty liver disease: diagnostic and therapeutic implications.

Authors:  Naim Alkhouri; Christine Carter-Kent; Ariel E Feldstein
Journal:  Expert Rev Gastroenterol Hepatol       Date:  2011-04       Impact factor: 3.869

4.  Comprehensive analysis of transcriptomics and metabolomics to understand triptolide-induced liver injury in mice.

Authors:  Jie Zhao; Cen Xie; Kanglong Wang; Shogo Takahashi; Kristopher W Krausz; Dasheng Lu; Qiong Wang; Yuhong Luo; Xianqiong Gong; Xiyan Mu; Qiao Wang; Suwen Su; Frank J Gonzalez
Journal:  Toxicol Lett       Date:  2020-08-21       Impact factor: 4.372

5.  The Bcl-2 homology domain 3 (BH3)-only proteins Bim and bid are functionally active and restrained by anti-apoptotic Bcl-2 family proteins in healthy liver.

Authors:  Takahiro Kodama; Hayato Hikita; Tsukasa Kawaguchi; Yoshinobu Saito; Satoshi Tanaka; Minoru Shigekawa; Satoshi Shimizu; Wei Li; Takuya Miyagi; Tatsuya Kanto; Naoki Hiramatsu; Tomohide Tatsumi; Tetsuo Takehara
Journal:  J Biol Chem       Date:  2013-08-28       Impact factor: 5.157

6.  Knockout of myeloid cell leukemia-1 induces liver damage and increases apoptosis susceptibility of murine hepatocytes.

Authors:  Binje Vick; Achim Weber; Toni Urbanik; Thorsten Maass; Andreas Teufel; Peter H Krammer; Joseph T Opferman; Marcus Schuchmann; Peter R Galle; Henning Schulze-Bergkamen
Journal:  Hepatology       Date:  2009-02       Impact factor: 17.425

  6 in total

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