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在人胚肾293(HEK-293)细胞中表达的M3型毒蕈碱型乙酰胆碱受体通过G12而非Gq型G蛋白向磷脂酶D发出信号:将G蛋白调节剂作为剖析受体-效应器偶联中对百日咳毒素有抗性的G蛋白的工具。

The M3 muscarinic acetylcholine receptor expressed in HEK-293 cells signals to phospholipase D via G12 but not Gq-type G proteins: regulators of G proteins as tools to dissect pertussis toxin-resistant G proteins in receptor-effector coupling.

作者信息

Rümenapp U, Asmus M, Schablowski H, Woznicki M, Han L, Jakobs K H, Fahimi-Vahid M, Michalek C, Wieland T, Schmidt M

机构信息

Institut für Pharmakologie, Universitätsklinikum Essen, Hufelandstrasse 55, D-45122 Essen, Germany.

出版信息

J Biol Chem. 2001 Jan 26;276(4):2474-9. doi: 10.1074/jbc.M004957200. Epub 2000 Oct 17.

Abstract

The M(3) muscarinic acetylcholine receptor (mAChR) expressed in HEK-293 cells couples to G(q) and G(12) proteins and stimulates phospholipase C (PLC) and phospholipase D (PLD) in a pertussis toxin-insensitive manner. To determine the type of G protein mediating M(3) mAChR-PLD coupling in comparison to M(3) mAChR-PLC coupling, we expressed various Galpha proteins and regulators of the G protein signaling (RGS), which act as GTPase-activating proteins for G(q)- or G(12)-type G proteins. PLD stimulation by the M(3) mAChR was enhanced by the overexpression of Galpha(12) and Galpha(13), whereas the overexpression of Galpha(q) strongly increased PLC activity without affecting PLD activity. Expression of the RGS homology domain of Lsc, which acts specifically on Galpha(12) and Galpha(13), blunted the M(3) mAChR-induced PLD stimulation without affecting PLC stimulation. On the other hand, overexpression of RGS4, which acts on Galpha(q)- but not Galpha(12)-type G proteins, suppressed the M(3) mAChR-induced PLC stimulation without altering PLD stimulation. We conclude that the M(3) mAChR in HEK-293 cells apparently signals to PLD via G(12)- but not G(q)-type G proteins and that G protein subtype-selective RGS proteins can be used as powerful tools to dissect the pertussis toxin-resistant G proteins and their role in receptor-effector coupling.

摘要

在HEK - 293细胞中表达的M(3)型毒蕈碱型乙酰胆碱受体(mAChR)与G(q)和G(12)蛋白偶联,并以百日咳毒素不敏感的方式刺激磷脂酶C(PLC)和磷脂酶D(PLD)。为了确定与M(3) mAChR - PLC偶联相比,介导M(3) mAChR - PLD偶联的G蛋白类型,我们表达了各种Gα蛋白和G蛋白信号调节剂(RGS),它们作为G(q)型或G(12)型G蛋白的GTP酶激活蛋白。Gα(12)和Gα(13)的过表达增强了M(3) mAChR对PLD的刺激,而Gα(q)的过表达强烈增加了PLC活性,而不影响PLD活性。特异性作用于Gα(12)和Gα(13)的Lsc的RGS同源结构域的表达减弱了M(3) mAChR诱导的PLD刺激,而不影响PLC刺激。另一方面,作用于Gα(q)型而非Gα(12)型G蛋白的RGS4的过表达抑制了M(3) mAChR诱导的PLC刺激,而不改变PLD刺激。我们得出结论,HEK - 293细胞中的M(3) mAChR显然通过G(12)型而非G(q)型G蛋白向PLD发出信号,并且G蛋白亚型选择性RGS蛋白可作为强大的工具来剖析百日咳毒素抗性G蛋白及其在受体 - 效应器偶联中的作用。

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