TY - JOUR
T1 - KCNQ5 channels control resting properties and release probability of a synapse
AU - Huang, Hai
AU - Trussell, Laurence O.
N1 - Funding Information:
We thank V. Balakrishnan and P. Brehm for comments, K. Bender and S. Kuo for technical advice and B. Kachar (National Institute on Deafness and Other Communication Disorders) for KCNQ4 antibody. L.O.T. is supported by US National Institutes of Health grants DC004450 and NS028901.
PY - 2011/7
Y1 - 2011/7
N2 - Little is known about which ion channels determine the resting electrical properties of presynaptic membranes. In recordings made from the rat calyx of Held, a giant mammalian terminal, we found resting potential to be controlled by KCNQ (Kv7) K+ channels, most probably KCNQ5 (Kv7.5) homomers. Unlike most KCNQ channels, which are activated only by depolarizing stimuli, the presynaptic channels began to activate just below the resting potential. As a result, blockers and activators of KCNQ5 depolarized or hyperpolarized nerve terminals, respectively, markedly altering resting conductance. Moreover, the background conductance set by KCNQ5 channels, together with Na+ and hyperpolarization-activated and cyclic nucleotide-gated (HCN) channels, determined the size and time course of the response to subthreshold stimuli. Signaling pathways known to directly affect exocytic machinery also regulated KCNQ5 channels, and increase or decrease of KCNQ5 channel activity controlled release probability through alterations in resting potential. Thus, ion channel determinants of presynaptic resting potential also control synaptic strength.
AB - Little is known about which ion channels determine the resting electrical properties of presynaptic membranes. In recordings made from the rat calyx of Held, a giant mammalian terminal, we found resting potential to be controlled by KCNQ (Kv7) K+ channels, most probably KCNQ5 (Kv7.5) homomers. Unlike most KCNQ channels, which are activated only by depolarizing stimuli, the presynaptic channels began to activate just below the resting potential. As a result, blockers and activators of KCNQ5 depolarized or hyperpolarized nerve terminals, respectively, markedly altering resting conductance. Moreover, the background conductance set by KCNQ5 channels, together with Na+ and hyperpolarization-activated and cyclic nucleotide-gated (HCN) channels, determined the size and time course of the response to subthreshold stimuli. Signaling pathways known to directly affect exocytic machinery also regulated KCNQ5 channels, and increase or decrease of KCNQ5 channel activity controlled release probability through alterations in resting potential. Thus, ion channel determinants of presynaptic resting potential also control synaptic strength.
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U2 - 10.1038/nn.2830
DO - 10.1038/nn.2830
M3 - Article
C2 - 21666672
AN - SCOPUS:79959660840
SN - 1097-6256
VL - 14
SP - 840
EP - 847
JO - Nature Neuroscience
JF - Nature Neuroscience
IS - 7
ER -