Results 131 to 140 of about 9,855 (254)

Modulation of Cx46 hemichannels by nitric oxide

open access: yesAmerican Journal of Physiology-Cell Physiology, 2009
Gap-junction hemichannels are composed of six protein subunits (connexins). Undocked hemichannels contribute to physiological autocrine/paracrine cell signaling, including release of signaling molecules, cell-volume regulation, and glucose uptake.
Retamal, Mauricio A.   +3 more
openaire   +5 more sources

Cx26 keratitis ichthyosis deafness syndrome mutations trigger alternative splicing of Cx26 to prevent expression and cause toxicity in vitro [PDF]

open access: yes, 2019
The Cx26 mRNA has not been reported to undergo alternative splicing. In expressing a series of human keratitis ichthyosis deafness (KID) syndrome mutations of Cx26 (A88V, N14K and A40V), we found the production of a truncated mRNA product.
Cook, Jonathan P.   +2 more
core   +1 more source

The role of pannexin hemichannels in inflammation and regeneration [PDF]

open access: yes, 2014
Tissue injury involves coordinated systemic responses including inflammatory response, targeted cell migration, cell-cell communication, stem cell activation and proliferation, and tissue inflammation and regeneration.
Helen P. Makarenkova   +1 more
core   +1 more source

Connexin-based gap junction hemichannels: Gating mechanisms

open access: yesBiochimica et Biophysica Acta (BBA) - Biomembranes, 2005
Connexins (Cxs) form hemichannels and gap junction channels. Each gap junction channel is composed of two hemichannels, also termed connexons, one from each of the coupled cells. Hemichannels are hexamers assembled in the ER, the Golgi, or a post Golgi compartment. They are transported to the cell surface in vesicles and inserted by vesicle fusion, and
Saez, JC   +4 more
openaire   +5 more sources

Ammonia mediates cortical hemichannel dysfunction in rodent models of chronic liver disease

open access: yesHepatology, 2017
The pathogenesis of hepatic encephalopathy (HE) in cirrhosis is multifactorial and ammonia is thought to play a key role. Astroglial dysfunction is known to be present in HE.
Anna Hadjihambi   +7 more
semanticscholar   +1 more source

Posttranslational Modifications in Connexins and Pannexins [PDF]

open access: yes, 2018
Posttranslational modification is a common cellular process that is used by cells to ensure a particular protein function. This can happen in a variety of ways, e.g., from the addition of phosphates or sugar residues to a particular amino acid, ensuring ...
Billaud, Marie   +4 more
core  

GLIAL HEMICHANNELS: A NEW ROUTE FOR CHEMICAL COMMUNICATION IN BRAIN [PDF]

open access: yes, 2008
The extracellular neurochemistry determines normal brain function and the faith of neurons after insults such as stroke. This thesis concerns the effect of extracellular events related to intense neuronal stimulation and stroke, i.e.
Stridh, Malin
core   +1 more source

Electrophysiology of Single and Aggregate Cx43 Hemichannels

open access: yesPLoS ONE, 2012
Connexin43 (Cx43) is the most ubiquitous gap junction protein in the human body and is essential for cell-to-cell communication in a variety of organs and organ systems. As a result, Cx43 is responsible for mediating both electrical and chemical signals, passing dissolved solutes and small signaling molecules between cells in a coordinated fashion ...
Cole Brokamp   +3 more
openaire   +3 more sources

Pannexin channel and connexin hemichannel expression in vascular function and inflammation

open access: yesBMC Cell Biology, 2017
Control of blood flow distribution and tissue homeostasis depend on the tight regulation of and coordination between the microvascular network and circulating blood cells.
Daniela Begandt   +6 more
semanticscholar   +1 more source

Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome

open access: yesScientific Reports, 2018
Germline missense mutations in GJB2 encoding connexin (Cx) 26 have been found in keratitis, ichthyosis and deafness (KID) syndrome. We explored the effects of three mouse Cx26 mutants (Cx26-G12R, -G45E and -D50N) corresponding to KID syndrome-causative ...
T. Taki   +3 more
semanticscholar   +1 more source

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