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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.

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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