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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
,
Xenbase
Barrio,
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
,
Xenbase
Contreras,
Metabolic inhibition induces opening of unapposed connexin 43 gap junction hemichannels and reduces gap junctional communication in cortical astrocytes in culture.
2002,
Pubmed
Cotrina,
ATP-mediated glia signaling.
2000,
Pubmed
Ebihara,
Properties of a nonjunctional current expressed from a rat connexin46 cDNA in Xenopus oocytes.
1993,
Pubmed
,
Xenbase
Ebihara,
New roles for connexons.
2003,
Pubmed
Eckert,
A distinct membrane current in rat lens fiber cells isolated under calcium-free conditions.
1998,
Pubmed
,
Xenbase
Foote,
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
,
Xenbase
Goodenough,
Beyond the gap: functions of unpaired connexon channels.
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