Literature DB >> 19275626

Hemichannels in cerebral ischemia.

Panagiotis Bargiotas1, Hannah Monyer, Markus Schwaninger.   

Abstract

Hemichannels are transmembrane channels that represent the functional subunits of gap junctions. Each hemichannel is composed of a connexin or pannexin hexamer and, after being transported to the membrane, remains unpaired until it is incorporated in a gap junction. Several studies have already provided evidence that gap junction-mediated intercellular diffusion of ions and small molecules during ischemia represents an important mechanism through which necrotic, apoptotic, or even protective signals are transported between cells. Although initially hemichannels were supposed to be functional only in gap junctions, recent findings indicate that unpaired hemichannels also display a large array of activities that can be modulated under several pathophysiological conditions, including ischemia. Open hemichannels in ischemia dramatically alter the permeability properties of membranes and lead to cell death through ionic dysregulation, loss of metabolites, and changes in intracellular ATP. This review focuses on the properties and possible functions of unpaired connexin and pannexin hemichannels and the implications this has for a variety of events, such as cell death, glutamate release, oxidative stress, cortical spreading depression, that occur during an ischemic insult and may affect its outcome.

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Year:  2009        PMID: 19275626     DOI: 10.2174/156652409787581646

Source DB:  PubMed          Journal:  Curr Mol Med        ISSN: 1566-5240            Impact factor:   2.222


  30 in total

1.  Pannexins in ischemia-induced neurodegeneration.

Authors:  Panagiotis Bargiotas; Antje Krenz; Sheriar G Hormuzdi; Dirk A Ridder; Anne Herb; Waleed Barakat; Silvia Penuela; Jakob von Engelhardt; Hannah Monyer; Markus Schwaninger
Journal:  Proc Natl Acad Sci U S A       Date:  2011-12-06       Impact factor: 11.205

Review 2.  Degradation of connexins through the proteasomal, endolysosomal and phagolysosomal pathways.

Authors:  Vivian Su; Kimberly Cochrane; Alan F Lau
Journal:  J Membr Biol       Date:  2012-07-08       Impact factor: 1.843

Review 3.  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

4.  Pannexin 1 constitutes the large conductance cation channel of cardiac myocytes.

Authors:  Marie-Cecile Kienitz; Kirsten Bender; Rolf Dermietzel; Lutz Pott; Georg Zoidl
Journal:  J Biol Chem       Date:  2010-11-01       Impact factor: 5.157

Review 5.  Gap junctions in inherited human disease.

Authors:  Georg Zoidl; Rolf Dermietzel
Journal:  Pflugers Arch       Date:  2010-02-07       Impact factor: 3.657

Review 6.  Neuronal P2X7 Receptors Revisited: Do They Really Exist?

Authors:  Peter Illes; Tahir Muhammad Khan; Patrizia Rubini
Journal:  J Neurosci       Date:  2017-07-26       Impact factor: 6.167

Review 7.  Connexin Channels at the Glio-Vascular Interface: Gatekeepers of the Brain.

Authors:  Marijke De Bock; Luc Leybaert; Christian Giaume
Journal:  Neurochem Res       Date:  2017-06-20       Impact factor: 3.996

8.  Mefloquine blockade of Pannexin1 currents: resolution of a conflict.

Authors:  Rodolfo Iglesias; David C Spray; Eliana Scemes
Journal:  Cell Commun Adhes       Date:  2009-12

9.  Permeation of calcium through purified connexin 26 hemichannels.

Authors:  Mariana C Fiori; Vania Figueroa; Maria E Zoghbi; Juan C Saéz; Luis Reuss; Guillermo A Altenberg
Journal:  J Biol Chem       Date:  2012-10-09       Impact factor: 5.157

Review 10.  Recent patents on novel P2X(7) receptor antagonists and their potential for reducing central nervous system inflammation.

Authors:  Scott A Friedle; Marjorie A Curet; Jyoti J Watters
Journal:  Recent Pat CNS Drug Discov       Date:  2010-01
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