Gap26, a connexin mimetic peptide, inhibits currents carried by connexin43 hemichannels and gap junction channels

T Desplantez, V Verma, L Leybaert, WH Evans… - Pharmacological …, 2012 - Elsevier
Connexin mimetic peptides corresponding to short conserved extracellular loop sequences
of connexins have been used widely as reversible inhibitors of gap junctional intercellular …

ATP amplifies NADPH-dependent and-independent neutrophil extracellular trap formation

A Sofoluwe, M Bacchetta, M Badaoui, BR Kwak… - Scientific reports, 2019 - nature.com
Neutrophils are the first immune cells to kill invading microbes at sites of infection using a
variety of processes, including the release of proteases, phagocytosis and the production of …

[HTML][HTML] Connexons and pannexons: newcomers in neurophysiology

G Cheung, O Chever, N Rouach - Frontiers in cellular neuroscience, 2014 - frontiersin.org
Connexin hemichannels are single membrane channels which have been traditionally
thought to work in pairs to form gap junction channels across two opposing cells. In …

[HTML][HTML] Pannexin 1 regulates bidirectional hippocampal synaptic plasticity in adult mice

AO Ardiles, C Flores-Muñoz, G Toro-Ayala… - Frontiers in cellular …, 2014 - frontiersin.org
The threshold for bidirectional modification of synaptic plasticity is known to be controlled by
several factors, including the balance between protein phosphorylation and …

Mechanisms linking connexin mutations to human diseases

JJ Kelly, J Simek, DW Laird - Cell and tissue research, 2015 - Springer
Ubiquitously expressed connexins are tetra-spanning transmembrane proteins that form
intercellular gap junction channels or cell surface hemichannels. Connexins share similar …

Connexin-mediated signaling in nonsensory cells is crucial for the development of sensory inner hair cells in the mouse cochlea

SL Johnson, F Ceriani, O Houston… - Journal of …, 2017 - Soc Neuroscience
Mutations in the genes encoding for gap junction proteins connexin 26 (Cx26) and connexin
30 (Cx30) have been linked to syndromic and nonsyndromic hearing loss in mice and …

[HTML][HTML] Research progress in delineating the pathological mechanisms of GJB2-related hearing loss

Y Wang, Y Jin, Q Zhang, Y Xiong, X Gu… - Frontiers in Cellular …, 2023 - frontiersin.org
Hearing loss is the most common congenital sensory impairment. Mutations or deficiencies
of the GJB2 gene are the most common genetic cause of congenital nonsyndromic …

[HTML][HTML] Keratitis-ichthyosis-deafness syndrome-associated Cx26 mutants produce nonfunctional gap junctions but hyperactive hemichannels when co-expressed …

IE García, J Maripillán, O Jara, R Ceriani… - Journal of Investigative …, 2015 - Elsevier
Mutations in Cx26 gene are found in most cases of human genetic deafness. Some
mutations produce syndromic deafness associated with skin disorders, like the Keratitis …

Physiological mechanisms for the modulation of pannexin 1 channel activity

JK Sandilos, DA Bayliss - The Journal of physiology, 2012 - Wiley Online Library
It is widely recognized that ATP, along with other nucleotides, subserves important
intercellular signalling processes. Among various nucleotide release mechanisms, the …

[HTML][HTML] ATP released from cardiac fibroblasts via connexin hemichannels activates profibrotic P2Y2 receptors

D Lu, S Soleymani, R Madakshire, PA Insel - The FASEB Journal, 2012 - ncbi.nlm.nih.gov
Cardiac fibroblasts (CFs) play an essential role in remodeling of the cardiac extracellular
matrix. Extracellular nucleotide signaling may provoke a profibrotic response in CFs. We …