Connexins: Mechanisms regulating protein levels and intercellular communication

被引:111
作者
Su, Vivian [1 ,2 ]
Lau, Alan F. [1 ,2 ,3 ]
机构
[1] Univ Hawaii Manoa, Pacific Biosci Res Ctr, Honolulu, HI 96822 USA
[2] Univ Hawaii, Ctr Canc, Canc Biol Program, Honolulu, HI 96813 USA
[3] Univ Hawaii Manoa, Dept Cell & Mol Biol, John A Burns Sch Med, Honolulu, HI 96822 USA
基金
美国国家卫生研究院;
关键词
Connexin; Proteasome; Lysosome; Autophagy; Degradation; Trafficking; GAP-JUNCTION PROTEIN; PROTEASOME-DEPENDENT DEGRADATION; LIVER EPITHELIAL-CELLS; BREAST-TUMOR CELLS; ENDOPLASMIC-RETICULUM; CONNEXIN43-INTERACTING PROTEIN; CYTOSOLIC STRESS; PLASMA-MEMBRANE; CARDIAC MYOCYTES; P53; DEGRADATION;
D O I
10.1016/j.febslet.2014.01.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Intercellular communication can occur through gap junction channels, which are comprised of connexin proteins. Therefore, levels of connexins can directly correlate with gap junctional intercellular communication. Because gap junctions have a critical role in maintaining cellular homeostasis, the regulation of connexin protein levels is important. In the connexin life cycle, connexin protein levels can be modified through differential gene transcription or altered through trafficking and degradation mechanisms. More recently, significant attention has been directed to the pathways that cells utilize to increase or decrease connexin levels and thus indirectly, gap junctional communication. Here, we review the studies revealing the mechanisms that affect connexin protein levels and gap junctional intercellular communication. (c) 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1212 / 1220
页数:9
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