Key result
Membrane stretch rapidly and reversibly inhibits rabbit atrial muscarinic potassium channels, a mechanosensitivity attributed to the Kir3.4 subunit.
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The Kir3.4 subunit is identified as the first stretch-inactivated potassium channel, providing a potential molecular basis for atrial volume-sensing.
Muscarinic potassium channels are heterotetramers of Kir3.1 and other Kir3 channel subunits and play major roles in regulating membrane excitability in cardiac atrial, neuronal, and neuroendocrine tissues. We report here that rabbit atrial muscarinic potassium channels are rapidly and reversibly inhibited by membrane stretch, possibly serving as a mechanoelectrical feedback pathway. To probe the molecular basis for this phenomenon, we heterologously expressed heteromeric Kir3.1/Kir3.4 channels in Xenopus oocytes and found that they possess similar mechanosensitivity in response to hypo-osmolar stress. This could be attributed in part, if not exclusively, to the Kir3.4 subunit, which reproduced the mechanosensitivity of the heteromeric channel when expressed as a homomeric channel in oocytes. Kir3.4 is the first stretch-inactivated potassium channel to be identified molecularly. Physiologically, this feature may be important in atrial volume-sensing and other responses to stretch.
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Ji et al. (1998) studied this question. Membrane stretch and hypo-osmolar stress was evaluated on Channel inhibition. Membrane stretch rapidly and reversibly inhibits rabbit atrial muscarinic potassium channels, a mechanosensitivity attributed to the Kir3.4 subunit.
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