Literature DB >> 19944606

The gap junction proteome and its relationship to disease.

Dale W Laird1.   

Abstract

In recent years our understanding of connexins has advanced from viewing them simply as proteins with a surprisingly short lifespan that form gap junction channels. Connexins are now known to be multifaceted proteins at the core of many multiprotein complexes that link to structural junctional complexes and cytoskeletal elements, and also to the cellular machinery that facilitates their transport, assembly, function and internalization. Collectively, these connexin-binding proteins can be termed the 'gap junction proteome'. The mechanistic understanding of the gap junction proteome with regards to the dynamic life cycle of connexins has grown further in importance in light of the large number of human diseases attributed to connexin gene mutations and regulatory changes in connexin spatial localization and expression levels.

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Year:  2009        PMID: 19944606     DOI: 10.1016/j.tcb.2009.11.001

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  117 in total

1.  Connexin37 and Connexin43 deficiencies in mice disrupt lymphatic valve development and result in lymphatic disorders including lymphedema and chylothorax.

Authors:  John D Kanady; Michael T Dellinger; Stephanie J Munger; Marlys H Witte; Alexander M Simon
Journal:  Dev Biol       Date:  2011-04-16       Impact factor: 3.582

2.  Gating of connexin 43 gap junctions by a cytoplasmic loop calmodulin binding domain.

Authors:  Qin Xu; Richard F Kopp; Yanyi Chen; Jenny J Yang; Michael W Roe; Richard D Veenstra
Journal:  Am J Physiol Cell Physiol       Date:  2012-03-14       Impact factor: 4.249

3.  Cytoplasmic amino acids within the membrane interface region influence connexin oligomerization.

Authors:  Tekla D Smith; Aditi Mohankumar; Peter J Minogue; Eric C Beyer; Viviana M Berthoud; Michael Koval
Journal:  J Membr Biol       Date:  2012-06-22       Impact factor: 1.843

4.  Blood cells and endothelial barrier function.

Authors:  Stephen F Rodrigues; D Neil Granger
Journal:  Tissue Barriers       Date:  2015-04-03

5.  Homotypic gap junctional communication associated with metastasis suppression increases with PKA activity and is unaffected by PI3K inhibition.

Authors:  Thomas M Bodenstine; Kedar S Vaidya; Aimen Ismail; Benjamin H Beck; Leah M Cook; Anne R Diers; Aimee Landar; Danny R Welch
Journal:  Cancer Res       Date:  2010-11-23       Impact factor: 12.701

Review 6.  Gap junctions.

Authors:  Morten Schak Nielsen; Lene Nygaard Axelsen; Paul L Sorgen; Vandana Verma; Mario Delmar; Niels-Henrik Holstein-Rathlou
Journal:  Compr Physiol       Date:  2012-07       Impact factor: 9.090

7.  Characterization of the connexin45 carboxyl-terminal domain structure and interactions with molecular partners.

Authors:  Jennifer L Kopanic; Mona H Al-mugotir; Fabien Kieken; Sydney Zach; Andrew J Trease; Paul L Sorgen
Journal:  Biophys J       Date:  2014-05-20       Impact factor: 4.033

8.  Injury-triggered Akt phosphorylation of Cx43: a ZO-1-driven molecular switch that regulates gap junction size.

Authors:  Clarence A Dunn; Paul D Lampe
Journal:  J Cell Sci       Date:  2013-11-08       Impact factor: 5.285

9.  Segregated Foxc2, NFATc1 and Connexin expression at normal developing venous valves, and Connexin-specific differences in the valve phenotypes of Cx37, Cx43, and Cx47 knockout mice.

Authors:  Stephanie J Munger; Xin Geng; R Sathish Srinivasan; Marlys H Witte; David L Paul; Alexander M Simon
Journal:  Dev Biol       Date:  2016-03-04       Impact factor: 3.582

10.  The role of the C-terminus in functional expression and internalization of rat connexin46 (rCx46).

Authors:  Barbara Schlingmann; Patrik Schadzek; Franziska Hemmerling; Frank Schaarschmidt; Alexander Heisterkamp; Anaclet Ngezahayo
Journal:  J Bioenerg Biomembr       Date:  2012-10-14       Impact factor: 2.945

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