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Gα(14) 将多种与G(i) 和G(s) 偶联的受体与磷脂酶C的激活联系起来。

Galpha(14) links a variety of G(i)- and G(s)-coupled receptors to the stimulation of phospholipase C.

作者信息

Ho M K, Yung L Y, Chan J S, Chan J H, Wong C S, Wong Y H

机构信息

Department of Biochemistry and the Biotechnology Research Institute, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China.

出版信息

Br J Pharmacol. 2001 Apr;132(7):1431-40. doi: 10.1038/sj.bjp.0703933.

DOI:10.1038/sj.bjp.0703933
PMID:11264236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1572686/
Abstract
  1. The bovine Galpha(14) is a member of the G(q) subfamily of G proteins that can regulate phospholipase Cbeta isoforms but the extent to which Galpha(14) recognizes different receptor classes is not known. 2. Galpha(14) was cotransfected with a variety of receptors in COS-7 cells, and agonist-induced stimulation of phospholipase C was then measured. 3. Activation of the type 2 but not type 1 somatostatin receptor in cells coexpressing Galpha(14) stimulated the accumulation of inositol phosphates; functional expression of both subtypes of somatostatin receptors was determined by the ability of somatostatin to inhibit cyclic AMP accumulation. 4. Among the three opioid receptors (mu, delta, and kappa), only the delta receptor was capable of stimulating IP formation when coexpressed with Galpha(14) in COS-7 cells. 5. A panel of G(i)- and G(s)-linked receptors was screened for their ability to stimulate IP accumulation via Galpha(14). The adenosine A(1), complement C5a, dopamine D(1), D(2) and D(5), formyl peptide, luteinizing hormone, secretin, and the three subtypes of melatonin (mt1, MT2, and Xenopus) receptors were all incapable of activating Galpha(14), while the alpha(2)- and beta(2)-adrenoceptors were able to do so. 6. Galpha(14)-mediated stimulation of phospholipase Cbeta was agonist dose-dependent. These data demonstrate that although Galpha(14) can interact with different classes of receptors, it is much less promiscuous than Galpha(15) or Galpha(16).
摘要
  1. 牛Gα(14)是G蛋白G(q)亚家族的成员,可调节磷脂酶Cβ亚型,但Gα(14)识别不同受体类别的程度尚不清楚。2. 将Gα(14)与多种受体共转染到COS-7细胞中,然后测量激动剂诱导的磷脂酶C刺激情况。3. 在共表达Gα(14)的细胞中,2型而非1型生长抑素受体的激活刺激了肌醇磷酸的积累;生长抑素受体两种亚型的功能表达通过生长抑素抑制环磷酸腺苷积累的能力来确定。4. 在三种阿片受体(μ、δ和κ)中,只有δ受体在与Gα(14)共表达于COS-7细胞时能够刺激肌醇磷酸的形成。5. 筛选了一组与G(i)和G(s)偶联的受体通过Gα(14)刺激肌醇磷酸积累的能力。腺苷A(1)、补体C5a、多巴胺D(1)、D(2)和D(5)、甲酰肽、促黄体生成素、促胰液素以及褪黑素的三种亚型(mt1、MT2和非洲爪蟾)受体均不能激活Gα(14),而α(2)和β(2)肾上腺素受体能够激活。6. Gα(14)介导的磷脂酶Cβ刺激呈激动剂剂量依赖性。这些数据表明,尽管Gα(14)可与不同类别的受体相互作用,但其混杂性远低于Gα(15)或Gα(16)。

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本文引用的文献

1
Preactivation permits subsequent stimulation of phospholipase C by G(i)-coupled receptors.预激活允许随后通过G(i)偶联受体刺激磷脂酶C。
Mol Pharmacol. 2000 Apr;57(4):700-8. doi: 10.1124/mol.57.4.700.
2
Incorporation of Galpha(z)-specific sequence at the carboxyl terminus increases the promiscuity of galpha(16) toward G(i)-coupled receptors.在羧基末端掺入Gα(z)特异性序列会增加Gα(16)对G(i)偶联受体的混杂性。
Mol Pharmacol. 2000 Jan;57(1):13-23.
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SSTR2A is the dominant somatostatin receptor subtype expressed by inflammatory cells, is widely expressed and directly regulates T cell IFN-gamma release.SSTR2A是炎症细胞表达的主要生长抑素受体亚型,广泛表达并直接调节T细胞γ干扰素的释放。
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GalphaL1 (Galpha14) couples the opioid receptor-like1 receptor to stimulation of phospholipase C.GαL1(Gα14)将阿片样物质受体样1受体与磷脂酶C的刺激偶联起来。
J Pharmacol Exp Ther. 1999 Jan;288(1):232-8.
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Regulation of cytokine and chemokine production by transmitters and co-transmitters of the autonomic nervous system.自主神经系统的递质和共递质对细胞因子和趋化因子产生的调节作用。
Biochem Pharmacol. 1998 Nov 1;56(9):1079-87. doi: 10.1016/s0006-2952(98)00153-1.
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Functional characterization of a series of mutant G protein alphaq subunits displaying promiscuous receptor coupling properties.一系列表现出混杂受体偶联特性的突变型G蛋白αq亚基的功能表征。
J Biol Chem. 1998 Jul 10;273(28):17886-92. doi: 10.1074/jbc.273.28.17886.
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Differential coupling of mu-, delta-, and kappa-opioid receptors to G alpha16-mediated stimulation of phospholipase C.μ、δ和κ阿片受体与Gα16介导的磷脂酶C刺激的差异偶联。
J Neurochem. 1998 May;70(5):2203-11.
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Switching of the coupling of the beta2-adrenergic receptor to different G proteins by protein kinase A.蛋白激酶A介导β2-肾上腺素能受体与不同G蛋白偶联的转换
Nature. 1997 Nov 6;390(6655):88-91. doi: 10.1038/36362.
10
Two basic amino acids in the second inner loop of the interleukin-8 receptor are essential for Galpha16 coupling.白细胞介素-8受体第二个内环中的两种碱性氨基酸对Gα16偶联至关重要。
J Biol Chem. 1997 Oct 3;272(40):24948-51. doi: 10.1074/jbc.272.40.24948.