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Alcohol modulation of BK channel gating depends on β subunit composition

In most mammalian tissues, Ca(2+)(i)/voltage-gated, large conductance K(+) (BK) channels consist of channel-forming slo1 and auxiliary (β1–β4) subunits. When Ca(2+)(i) (3–20 µM) reaches the vicinity of BK channels and increases their activity at physiological voltages, β1- and β4-containing BK chann...

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Detalles Bibliográficos
Autores principales: Kuntamallappanavar, Guruprasad, Dopico, Alex M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089933/
https://www.ncbi.nlm.nih.gov/pubmed/27799321
http://dx.doi.org/10.1085/jgp.201611594
Descripción
Sumario:In most mammalian tissues, Ca(2+)(i)/voltage-gated, large conductance K(+) (BK) channels consist of channel-forming slo1 and auxiliary (β1–β4) subunits. When Ca(2+)(i) (3–20 µM) reaches the vicinity of BK channels and increases their activity at physiological voltages, β1- and β4-containing BK channels are, respectively, inhibited and potentiated by intoxicating levels of ethanol (50 mM). Previous studies using different slo1s, lipid environments, and Ca(2+)(i) concentrations—all determinants of the BK response to ethanol—made it impossible to determine the specific contribution of β subunits to ethanol action on BK activity. Furthermore, these studies measured ethanol action on ionic current under a limited range of stimuli, rendering no information on the gating processes targeted by alcohol and their regulation by βs. Here, we used identical experimental conditions to obtain single-channel and macroscopic currents of the same slo1 channel (“cbv1” from rat cerebral artery myocytes) in the presence and absence of 50 mM ethanol. First, we assessed the role five different β subunits (1,2,2-IR, 3-variant d, and 4) in ethanol action on channel function. Thus, two phenotypes were identified: (1) ethanol potentiated cbv1-, cbv1+β3-, and cbv1+β4-mediated currents at low Ca(2+)(i) while inhibiting current at high Ca(2+)(i), the potentiation–inhibition crossover occurring at 20 µM Ca(2+)(i); (2) for cbv1+β1, cbv1+wt β2, and cbv1+β2-IR, this crossover was shifted to ∼3 µM Ca(2+)(i). Second, applying Horrigan–Aldrich gating analysis on both phenotypes, we show that ethanol fails to modify intrinsic gating and the voltage-dependent parameters under examination. For cbv1, however, ethanol (a) drastically increases the channel’s apparent Ca(2+) affinity (nine-times decrease in K(d)) and (b) very mildly decreases allosteric coupling between Ca(2+) binding and channel opening (C). The decreased K(d) leads to increased channel activity. For cbv1+β1, ethanol (a) also decreases K(d), yet this decrease (two times) is much smaller than that of cbv1; (b) reduces C; and (c) decreases coupling between Ca(2+) binding and voltage sensing (parameter E). Decreased allosteric coupling leads to diminished BK activity. Thus, we have identified critical gating modifications that lead to the differential actions of ethanol on slo1 with and without different β subunits.