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Proc Natl Acad Sci U S A
2003 Dec 23;10026:16030-5. doi: 10.1073/pnas.2530348100.
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Molecular basis of calcium regulation in connexin-32 hemichannels.
Gómez-Hernández JM, de Miguel M, Larrosa B, González D, Barrio LC.
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In addition to forming gap-junction channels, a subset of connexins (Cxs) also form functional hemichannels. Most hemichannels are activated by depolarization, and opening depends critically on the external Ca2+ concentration. Here we describe the mechanisms of action and the structural determinants underlying the Ca2+ regulation of Cx32 hemichannels. At millimolar calcium concentrations, hemichannel voltage gating to the full open state of approximately 90 pS is inhibited, and ion conduction at negative voltages of the partially open hemichannels ( approximately 18 pS) is blocked. Thus, divalent cation blockage should be considered as a physiological mechanism to protect the cell from the potentially adverse effects of leaky hemichannels. A ring of 12 Asp residues within the external vestibule of the pore is responsible for the binding of Ca2+ that accounts for both pore occlusion and blockage of gating. The residue Asp-169 of one subunit and the Asp-178 of an adjacent subunit must be arranged precisely to allow interactions with Ca2+ to occur. Interestingly, a naturally occurring mutation (D178Y) that causes an inherited peripheral neuropathy induces a complete Ca2+ deregulation of Cx32 hemichannel activity, suggesting that this dysfunction may be involved in the pathogenesis of the neuropathy.
Abrams,
Voltage opens unopposed gap junction hemichannels formed by a connexin 32 mutant associated with X-linked Charcot-Marie-Tooth disease.
2002, Pubmed,
Xenbase
Abrams,
Voltage opens unopposed gap junction hemichannels formed by a connexin 32 mutant associated with X-linked Charcot-Marie-Tooth disease.
2002,
Pubmed
,
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Gap junctions formed by connexins 26 and 32 alone and in combination are differently affected by applied voltage.
1991,
Pubmed
,
Xenbase Bergoffen,
Connexin mutations in X-linked Charcot-Marie-Tooth disease.
1993,
Pubmed Bone,
Connexin32 and X-linked Charcot-Marie-Tooth disease.
1997,
Pubmed Bruzzone,
Connexin 43 hemi channels mediate Ca2+-regulated transmembrane NAD+ fluxes in intact cells.
2001,
Pubmed Castro,
Altered formation of hemichannels and gap junction channels caused by C-terminal connexin-32 mutations.
1999,
Pubmed
,
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Metabolic inhibition induces opening of unapposed connexin 43 gap junction hemichannels and reduces gap junctional communication in cortical astrocytes in culture.
2002,
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ATP-mediated glia signaling.
2000,
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Properties of a nonjunctional current expressed from a rat connexin46 cDNA in Xenopus oocytes.
1993,
Pubmed
,
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2003,
Pubmed Eckert,
A distinct membrane current in rat lens fiber cells isolated under calcium-free conditions.
1998,
Pubmed
,
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The pattern of disulfide linkages in the extracellular loop regions of connexin 32 suggests a model for the docking interface of gap junctions.
1998,
Pubmed
,
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2003,
Pubmed Harris,
Emerging issues of connexin channels: biophysics fills the gap.
2001,
Pubmed Janssen-Bienhold,
Identification and localization of connexin26 within the photoreceptor-horizontal cell synaptic complex.
2001,
Pubmed John,
Connexin-43 hemichannels opened by metabolic inhibition.
1999,
Pubmed Kamermans,
Hemichannel-mediated inhibition in the outer retina.
2001,
Pubmed Kondo,
Metabolic inhibition activates a non-selective current through connexin hemichannels in isolated ventricular myocytes.
2000,
Pubmed Li,
Properties and regulation of gap junctional hemichannels in the plasma membranes of cultured cells.
1996,
Pubmed Müller,
Conformational changes in surface structures of isolated connexin 26 gap junctions.
2002,
Pubmed Musil,
Multisubunit assembly of an integral plasma membrane channel protein, gap junction connexin43, occurs after exit from the ER.
1993,
Pubmed
,
Xenbase Oh,
Molecular determinants of electrical rectification of single channel conductance in gap junctions formed by connexins 26 and 32.
1999,
Pubmed Oh,
Changes in permeability caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease.
1997,
Pubmed
,
Xenbase Paul,
Connexin46, a novel lens gap junction protein, induces voltage-gated currents in nonjunctional plasma membrane of Xenopus oocytes.
1991,
Pubmed
,
Xenbase Pfahnl,
A chimeric connexin forming gap junction hemichannels.
1997,
Pubmed
,
Xenbase Pfahnl,
Gating of cx46 gap junction hemichannels by calcium and voltage.
1999,
Pubmed
,
Xenbase Plotkin,
Transduction of cell survival signals by connexin-43 hemichannels.
2002,
Pubmed Rash,
Cell-specific expression of connexins and evidence of restricted gap junctional coupling between glial cells and between neurons.
2001,
Pubmed Root,
Identification of an external divalent cation-binding site in the pore of a cGMP-activated channel.
1993,
Pubmed
,
Xenbase Somjen,
Mechanisms of spreading depression and hypoxic spreading depression-like depolarization.
2001,
Pubmed Unger,
Three-dimensional structure of a recombinant gap junction membrane channel.
1999,
Pubmed Unwin,
Two configurations of a channel-forming membrane protein.
,
Pubmed Venance,
Connexin expression in electrically coupled postnatal rat brain neurons.
2000,
Pubmed Willecke,
Structural and functional diversity of connexin genes in the mouse and human genome.
2002,
Pubmed Yang,
Molecular determinants of Ca2+ selectivity and ion permeation in L-type Ca2+ channels.
1993,
Pubmed
,
Xenbase