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M3型毒蕈碱型乙酰胆碱受体刺激的磷脂酶D的快速持续脱敏。同时伴有磷脂酶C的敏化。

Rapid and persistent desensitization of m3 muscarinic acetylcholine receptor-stimulated phospholipase D. Concomitant sensitization of phospholipase C.

作者信息

Schmidt M, Fasselt B, Rümenapp U, Bienek C, Wieland T, van Koppen C J, Jakobs K H

机构信息

Institut für Pharmakologie, Universität GH Essen, Germany.

出版信息

J Biol Chem. 1995 Aug 25;270(34):19949-56. doi: 10.1074/jbc.270.34.19949.

Abstract

Activation of muscarinic acetylcholine receptors (mAChR) in human embryonic kidney (HEK) cells stably expressing the human m3 subtype leads to stimulation of both phospholipase C (PLC) and D (PLD). mAChR-stimulated PLD was turned off after 2 min of receptor activation with either the full (carbachol) or partial agonist (pilocarpine) and remained completely suppressed for at least 4 h. Partial recovery was observed 24 h after agonist removal. This rapid arrest of PLD response was not due to a loss of cell surface receptors and was also not caused by negative feedback due to concomitant activation of protein kinase C, tyrosine phosphorylation, increase in cytosolic calcium, or activation of Gi proteins. Furthermore, PLD stimulation by directly activated protein kinase C and GTP-binding proteins was unaltered in carbachol-pretreated cells. Finally, neither prevention of PLD stimulation during carbachol pretreatment by genistein nor inhibition of protein synthesis by cycloheximide, added before or after carbachol challenge, resulted in recovery of mAChR-stimulated PLD. The short term carbachol pretreatment nearly completely abolished agonist-induced binding of guanosine 5'-O-(3-thiotriphosphate) to membranes or permeabilized adherent cells. Full recovery of this response was achieved after 4 h. Similar to transfected m3 mAChR, PLD stimulation by endogenously expressed purinergic receptors was also fully blunted after 2 min of agonist (ATP) treatment. Preexposure of HEK cells to either receptor agonist partially, but not completely, reduced PLD stimulation by the other agonist. In contrast to desensitization of PLD stimulation, 2 min of carbachol treatment led to a sensitization, by up to 2-fold, of mAChR-stimulated inositol phosphate formation. This supersensitivity was also observed with pilocarpine, which acted as a full agonist on PLC. On the basis of these results, we conclude that the m3 mAChR stimulates PLD and PLC in HEK cells with distinct efficiencies and with very distinct durations of each response. The rapid and long lasting desensitization of the PLD response is apparently not due to a loss of cell surface receptors or PLD activation by GTP-binding proteins, but it may involve, at least initially, an uncoupling of receptors from GTP-binding proteins and most likely a loss of an as yet undefined essential transducing component.

摘要

在稳定表达人m3亚型的人胚肾(HEK)细胞中,毒蕈碱型乙酰胆碱受体(mAChR)的激活会导致磷脂酶C(PLC)和磷脂酶D(PLD)的刺激。用完全激动剂(卡巴胆碱)或部分激动剂(毛果芸香碱)激活受体2分钟后,mAChR刺激的PLD活性关闭,并在至少4小时内完全受到抑制。激动剂去除24小时后观察到部分恢复。PLD反应的这种快速终止不是由于细胞表面受体的丧失,也不是由于蛋白激酶C的伴随激活、酪氨酸磷酸化、胞质钙增加或Gi蛋白激活导致的负反馈。此外,在卡巴胆碱预处理的细胞中,直接激活的蛋白激酶C和GTP结合蛋白对PLD的刺激没有改变。最后,无论是在卡巴胆碱预处理期间用染料木黄酮预防PLD刺激,还是在卡巴胆碱刺激之前或之后用环己酰亚胺抑制蛋白质合成,都没有导致mAChR刺激的PLD活性恢复。短期卡巴胆碱预处理几乎完全消除了激动剂诱导的鸟苷5'-O-(3-硫代三磷酸)与膜或透化贴壁细胞的结合。4小时后该反应完全恢复。与转染的m3 mAChR类似,在用激动剂(ATP)处理2分钟后,内源性表达的嘌呤能受体对PLD的刺激也完全减弱。将HEK细胞预先暴露于任一受体激动剂会部分但不完全降低另一种激动剂对PLD的刺激。与PLD刺激的脱敏相反,2分钟的卡巴胆碱处理导致mAChR刺激的肌醇磷酸形成致敏,最高可达2倍。毛果芸香碱作为PLC的完全激动剂时也观察到了这种超敏反应。基于这些结果,我们得出结论,m3 mAChR以不同的效率和非常不同的反应持续时间刺激HEK细胞中的PLD和PLC。PLD反应的快速和持久脱敏显然不是由于细胞表面受体的丧失或GTP结合蛋白对PLD的激活,而是至少在最初可能涉及受体与GTP结合蛋白的解偶联,并且很可能是一种尚未确定的必需转导成分的丧失。

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