TY - JOUR
T1 - PIP2 activates KCNQ channels, and its hydrolysis underlies receptor-mediated inhibition of M currents
AU - Zhang, Hailin
AU - Craciun, Liviu C.
AU - Mirshahi, Tooraj
AU - Rohács, Tibor
AU - Lopes, Coeli M.B.
AU - Jin, Taihao
AU - Logothetis, Diomedes E.
N1 - Funding Information:
This work was supported from NIH grant HL-59949 to D.E.L. D.E.L. is an Established Investigator of the American Heart Association. H.Z. was supported by NSFC (National Natural Science Foundation of China) grants 30240001 and 30270361. T.M. was supported by NRSA grant HL10307, T.R. by both NRSA grant GM20856 and a Charles H. Revson Fellowship, and C.M.B.L. by AHA grant 0225664T.
PY - 2003/3/27
Y1 - 2003/3/27
N2 - KCNQ channels belong to a family of potassium ion channels with crucial roles in physiology and disease. Heteromers of KCNQ2/3 subunits constitute the neuronal M channels. Inhibition of M currents, by pathways that stimulate phospholipase C activity, controls excitability throughout the nervous system. Here we show that a common feature of all KCNQ channels is their activation by the signaling membrane phospholipid phosphatidylinositol-bis-phosphate (PIP2). We show that wortmannin, at concentrations that prevent recovery from receptor-mediated inhibition of M currents, blocks PIP2 replenishment to the cell surface. Moreover, we identify a C-terminal histidine residue, immediately proximal to the plasma membrane, mutation of which renders M channels less sensitive to PIP2 and more sensitive to receptor-mediated inhibition. Finally, native or recombinant channels inhibited by muscarinic agonists can be activated by PIP2. Our data strongly suggest that PIP2 acts as a membrane-diffusible second messenger to regulate directly the activity of KCNQ currents.
AB - KCNQ channels belong to a family of potassium ion channels with crucial roles in physiology and disease. Heteromers of KCNQ2/3 subunits constitute the neuronal M channels. Inhibition of M currents, by pathways that stimulate phospholipase C activity, controls excitability throughout the nervous system. Here we show that a common feature of all KCNQ channels is their activation by the signaling membrane phospholipid phosphatidylinositol-bis-phosphate (PIP2). We show that wortmannin, at concentrations that prevent recovery from receptor-mediated inhibition of M currents, blocks PIP2 replenishment to the cell surface. Moreover, we identify a C-terminal histidine residue, immediately proximal to the plasma membrane, mutation of which renders M channels less sensitive to PIP2 and more sensitive to receptor-mediated inhibition. Finally, native or recombinant channels inhibited by muscarinic agonists can be activated by PIP2. Our data strongly suggest that PIP2 acts as a membrane-diffusible second messenger to regulate directly the activity of KCNQ currents.
UR - http://www.scopus.com/inward/record.url?scp=0037468826&partnerID=8YFLogxK
U2 - 10.1016/S0896-6273(03)00125-9
DO - 10.1016/S0896-6273(03)00125-9
M3 - Article
C2 - 12670425
AN - SCOPUS:0037468826
SN - 0896-6273
VL - 37
SP - 963
EP - 975
JO - Neuron
JF - Neuron
IS - 6
ER -