Literature DB >> 12566218

Connexins, gap junctional intercellular communication and kinases.

Véronique Cruciani1, Svein Ole Mikalsen.   

Abstract

A number of kinases and signal transduction pathways are known to affect gap junctional intercellular communication and/or phosphorylation of connexins. Most of the information is available for protein kinase A, protein kinase C, mitogen-activated protein kinase, and the tyrosine kinase Src. Much less is known for protein kinase G, Ca(2+)-calmodulin dependent protein kinase, and casein kinase. However, the present lack of knowledge is not necessarily synonymous with lack of importance in the regulation of intercellular communication and phosphorylation of connexins. Kinases and the phosphorylation of connexins may be involved in the regulation of gap junctional intercellular communication at all levels ranging from the expression of connexin genes to the degradation of the gap junction channels. The exact role of the phosphorylation depends both on the kinase and the connexin involved, as well as the cellular context.

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Year:  2002        PMID: 12566218     DOI: 10.1016/s0248-4900(02)00014-x

Source DB:  PubMed          Journal:  Biol Cell        ISSN: 0248-4900            Impact factor:   4.458


  18 in total

Review 1.  Regulation of gap junctions by tyrosine protein kinases.

Authors:  Bonnie J Warn-Cramer; Alan F Lau
Journal:  Biochim Biophys Acta       Date:  2004-03-23

Review 2.  Gap junctions or hemichannel-dependent and independent roles of connexins in cataractogenesis and lens development.

Authors:  J X Jiang
Journal:  Curr Mol Med       Date:  2010-12       Impact factor: 2.222

Review 3.  Lens gap junctions in growth, differentiation, and homeostasis.

Authors:  Richard T Mathias; Thomas W White; Xiaohua Gong
Journal:  Physiol Rev       Date:  2010-01       Impact factor: 37.312

4.  Biphasic increase of gap junction coupling induced by dipyridamole in the rat aortic A-10 vascular smooth muscle cell line.

Authors:  Daniela Begandt; Almke Bader; Lutz Dreyer; Natalie Eisert; Thilo Reeck; Anaclet Ngezahayo
Journal:  J Cell Commun Signal       Date:  2013-03-13       Impact factor: 5.782

5.  Dipyridamole-related enhancement of gap junction coupling in the GM-7373 aortic endothelial cells correlates with an increase in the amount of connexin 43 mRNA and protein as well as gap junction plaques.

Authors:  Daniela Begandt; Almke Bader; Linda Gerhard; Julia Lindner; Lutz Dreyer; Barbara Schlingmann; Anaclet Ngezahayo
Journal:  J Bioenerg Biomembr       Date:  2013-06-26       Impact factor: 2.945

6.  Phosphorylation of connexin 50 by protein kinase A enhances gap junction and hemichannel function.

Authors:  Jialu Liu; Jose F Ek Vitorin; Susan T Weintraub; Sumin Gu; Qian Shi; Janis M Burt; Jean X Jiang
Journal:  J Biol Chem       Date:  2011-03-24       Impact factor: 5.157

7.  An intact connexin43 is required to enhance signaling and gene expression in osteoblast-like cells.

Authors:  Carla Hebert; Joseph P Stains
Journal:  J Cell Biochem       Date:  2013-11       Impact factor: 4.429

8.  Dipyridamole increases gap junction coupling in bovine GM-7373 aortic endothelial cells by a cAMP-protein kinase A dependent pathway.

Authors:  D Begandt; W Bintig; K Oberheide; S Schlie; A Ngezahayo
Journal:  J Bioenerg Biomembr       Date:  2010-01-07       Impact factor: 2.945

9.  The metabolic inhibitor antimycin A can disrupt cell-to-cell communication by an ATP- and Ca(2+)-independent mechanism.

Authors:  Isabelle Plaisance; Fabien Duthe; Denis Sarrouilhe; Jean-Claude Hervé
Journal:  Pflugers Arch       Date:  2003-09-19       Impact factor: 3.657

10.  Clinically relevant concentrations of di (2-ethylhexyl) phthalate (DEHP) uncouple cardiac syncytium.

Authors:  Nikki Gillum; Zaruhi Karabekian; Luther M Swift; Ronald P Brown; Matthew W Kay; Narine Sarvazyan
Journal:  Toxicol Appl Pharmacol       Date:  2009-01-22       Impact factor: 4.219

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