首页> 外文期刊>The Journal of Physiology >Role of receptor kinase in short-term desensitization of cardiac muscarinic K+ channels expressed in Chinese hamster ovary cells.
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Role of receptor kinase in short-term desensitization of cardiac muscarinic K+ channels expressed in Chinese hamster ovary cells.

机译:受体激酶在中国仓鼠卵巢细胞中表达的心肌毒蕈碱钾通道短期脱敏中的作用。

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摘要

1. The cardiac muscarinic receptor-K+ channel system was reconstructed in Chinese hamster ovary (CHO) cells by transfecting the cells with the various components of the system. The activity of the muscarinic K+ channel was measured with the cell-attached configuration of the patch clamp technique. 2. In CHO cells transfected with the channel (Kir3.1/Kir3.4), receptor (hm2) and receptor kinase (GRK2), on exposure to agonist, there was a decline in channel activity as a result of desensitization, similar to that in atrial cells. 3. Whereas the desensitization was almost abolished by not transfecting with the receptor kinase or by transfecting with a mutant receptor lacking phosphorylation sites, it was only reduced (by approximately 39%) by transfecting with a mutant receptor kinase with little/kinase activity. 4. These results suggest that the receptor kinase is responsible for desensitization of the muscarinic K+ channel and that this involves phosphorylation-dependent and -independent mechanisms.
机译:1.通过用系统的各种成分转染细胞,在中国仓鼠卵巢(CHO)细胞中重建心脏毒蕈碱受体K +通道系统。毒蕈碱钾离子通道的活性通过膜片钳技术的细胞附着结构进行测量。 2.在暴露于激动剂后,经通道(Kir3.1 / Kir3.4),受体(hm2)和受体激酶(GRK2)转染的CHO细胞中,由于脱敏而导致的通道活性下降,类似于在心房细胞中。 3.尽管通过不用受体激酶转染或通过用缺少磷酸化位点的突变受体转染几乎消除了脱敏,但是通过用几乎没有/激酶活性的突变受体激酶转染仅使脱敏减少(约39%)。 4.这些结果表明受体激酶引起毒蕈碱K +通道的脱敏,并且这涉及磷酸化依赖性和非依赖性机制。

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