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This Article Full Text Full Text (PDF) All Versions of this Article: 586/7/1811    most recent jphysiol.2007.148304v1 Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Google Scholar Articles by Hernandez, C. C. Articles by Shapiro, M. S. PubMed PubMed Citation Articles by Hernandez, C. C. Articles by Shapiro, M. S. Related Collections Review articles Neuroscience

¹ University of Texas Health Science Center at San Antonio, Department of Physiology, MS 7756, San Antonio, TX 78229, USA

Neural M-type (KCNQ/Kv7) K⁺ channels control somatic excitability, bursting and neurotransmitter release throughout the nervous system. Their activity is regulated by multiple signalling pathways. In superior cervical ganglion sympathetic neurons, muscarinic M₁, angiotensin II AT₁, bradykinin B₂ and purinergic P2Y agonists suppress M current (I_M). Probes of PLC activity show agonists of all four receptors to induce robust PIP₂ hydrolysis. We have grouped these receptors into two related modes of action. One mode involves depletion of phosphatidylinositol 4,5-bisphosphate (PIP₂) in the membrane, whose interaction with the channels is thought necessary for their function. The other involves IP₃-mediated intracellular Ca²⁺ signals that stimulate PIP₂ synthesis, preventing its depletion, and suppress I_M via calmodulin. Carbon-fibre amperometry can evaluate the effect of M channel activity on release of neurotransmitter. Consistent with the dominant role of M current in control of neuronal discharge, M channel openers, or blockers, reduced or augmented the evoked release of noradrenaline neurotransmitter from superior cervical ganglion (SCG) neurons, respectively. We seek to localize the subdomains on the channels critical to their regulation by PIP₂. Based on single-channel recordings from chimeras between high-PIP₂ affinity KCNQ3 and low-PIP₂ affinity KCNQ4 channels, we focus on a 57-residue domain within the carboxy-terminus that is a possible PIP₂ binding site. Homology modelling of this domain using the published structure of IRK1 channels as a template predicts a structure very similar to an analogous region in IRK1 channels, and shows a cluster of basic residues in the KCNQ2 domain to correspond to those implicated in PIP₂ regulation of Kir channels. We discuss some important issues dealing with these topics.

(Received 15 November 2007; accepted after revision 25 January 2008; first published online 31 January 2008)
Corresponding author M. S. Shapiro: University of Texas Health Science Center at San Antonio, Department of Physiology, MS 7756, San Antonio, TX 78229, USA.  Email: shapirom{at}uthscsa.edu

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