Search Results - "Sanchez, Helmuth A"
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Supporting Cells and Their Potential Roles in Cisplatin-Induced Ototoxicity
Published in Frontiers in neuroscience (27-04-2022)“…Cisplatin is a known ototoxic chemotherapy drug, causing irreversible hearing loss. Evidence has shown that cisplatin causes inner ear damage as a result of…”
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2
The D50N mutation and syndromic deafness: altered Cx26 hemichannel properties caused by effects on the pore and intersubunit interactions
Published in The Journal of general physiology (01-07-2013)“…Mutations in the GJB2 gene, which encodes Cx26, are the most common cause of sensorineural deafness. In syndromic cases, such as keratitis-ichthyosis-deafness…”
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3
Restraint of Human Skin Fibroblast Motility, Migration, and Cell Surface Actin Dynamics, by Pannexin 1 and P2X7 Receptor Signaling
Published in International journal of molecular sciences (22-01-2021)“…Wound healing is a dynamic process required to maintain skin integrity and which relies on the precise migration of different cell types. A key molecule that…”
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4
An Update on Connexin Gap Junction and Hemichannels in Diabetic Retinopathy
Published in International journal of molecular sciences (21-03-2021)“…Diabetic retinopathy (DR) is one of the main causes of vision loss in the working age population. It is characterized by a progressive deterioration of the…”
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Hemichannels in the neurovascular unit and white matter under normal and inflamed conditions
Published in CNS & neurological disorders drug targets (01-05-2011)“…In the normal brain, cellular types that compose the neurovascular unit, including neurons, astrocytes and endothelial cells express pannexins and connexins,…”
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Expression of KID syndromic mutation Cx26S17F produces hyperactive hemichannels in supporting cells of the organ of Corti
Published in Frontiers in cell and developmental biology (09-01-2023)“…Some mutations in gap junction protein Connexin 26 (Cx26) lead to syndromic deafness, where hearing impairment is associated with skin disease, like in…”
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A pore locus in the E1 domain differentially regulates Cx26 and Cx30 hemichannel function
Published in The Journal of general physiology (04-11-2024)“…Connexins (Cxs) function as gap junction (GJ) channels and hemichannels that mediate intercellular and transmembrane signaling, respectively. Here, we…”
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Role of connexin-based gap junction channels and hemichannels in ischemia-induced cell death in nervous tissue
Published in Brain Research Reviews (01-12-2004)“…Gap junction channels and hemichannels formed of connexin subunits are found in most cell types in vertebrates. Gap junctions connect cells via channels not…”
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Inflammatory conditions induce gap junctional communication between rat Kupffer cells both in vivo and in vitro
Published in Cellular immunology (01-06-2007)“…Connexin43 (Cx43), a gap junction protein subunit, has been previously detected in Kupffer cells (KCs) during liver inflammation, however, KCs phagocytose cell…”
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Syndromic deafness mutations at Asn 14 differentially alter the open stability of Cx26 hemichannels
Published in The Journal of general physiology (01-07-2016)“…Connexin 26 (Cx26) is a transmembrane protein that forms hexameric hemichannels that can function when unopposed or dock to form intercellular gap junction…”
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Connexin 43 hemichannels mediate the Ca2+ influx induced by extracellular alkalinization
Published in American Journal of Physiology: Cell Physiology (01-12-2010)“…Although alkaline pH is known to trigger Ca(2+) influx in diverse cells, no pH-sensitive Ca(2+) channel has been identified. Here, we report that extracellular…”
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Altered Inhibition of Cx26 Hemichannels by pH and Zn2+ in the A40V Mutation Associated with Keratitis-Ichthyosis-Deafness Syndrome
Published in The Journal of biological chemistry (01-08-2014)“…Excessive opening of undocked Cx26 hemichannels in the plasma membrane is associated with disease pathogenesis in keratitis-ichthyosis-deafness (KID) syndrome…”
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Aberrant Cx26 hemichannels and keratitis-ichthyosis-deafness syndrome: insights into syndromic hearing loss
Published in Frontiers in cellular neuroscience (27-10-2014)“…Mutation of the GJB2 gene, which encodes the connexin 26 (Cx26) gap junction (GJ) protein, is the most common cause of hereditary, sensorineural hearing loss…”
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14
Redox-mediated regulation of connexin proteins; focus on nitric oxide
Published in Biochimica et biophysica acta. Biomembranes (01-01-2018)“…Connexins are membrane proteins that form hemichannels and gap junction channels at the plasma membrane. Through these channels connexins participate in…”
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15
MATE1 expression in the cochlea and its potential involvement in cisplatin cellular uptake and ototoxicity
Published in Acta oto-laryngologica (01-03-2023)“…Cisplatin appears to enter the cochlear cells through the organic cation transporter 2 (OCT2). There is recent evidence that multidrug and toxin extrusion…”
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Metabolic inhibition increases activity of connexin-32 hemichannels permeable to Ca2+ in transfected HeLa cells
Published in American Journal of Physiology: Cell Physiology (01-09-2009)“…Numerous cell types express functional connexin (Cx) hemichannels (HCs), and membrane depolarization and/or exposure to a divalent cation-free bathing solution…”
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Mechanism of inhibition of connexin channels by the quinine derivative N-benzylquininium
Published in The Journal of general physiology (01-01-2012)“…The anti-malarial drug quinine and its quaternary derivative N-benzylquininium (BQ(+)) have been shown to inhibit gap junction (GJ) channels with specificity…”
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Regulation of intercellular calcium signaling through calcium interactions with connexin-based channels
Published in Advances in experimental medicine and biology (01-01-2012)“…The synchronization of numerous cellular events requires complex electric and metabolic cell-cell interactions. Connexins are a family of membrane proteins…”
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Differentially altered Ca2+ regulation and Ca2+ permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome
Published in The Journal of general physiology (01-07-2010)“…Mutations in GJB2, which encodes Cx26, are one of the most common causes of inherited deafness in humans. More than 100 mutations have been identified…”
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Mechanism of inhibition of connexin channels by the quinine derivative N-benzylquininium
Published in The Journal of general physiology (01-01-2011)“…The anti-malarial drug quinine and its quaternary derivative N-benzylquininium (BQ+) have been shown to inhibit gap junction (GJ) channels with specificity for…”
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