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人神经母细胞瘤SH-SY5Y细胞中M3型毒蕈碱受体和α1B肾上腺素能受体与Gαq/11的同源和异源解偶联

Homologous and heterologous uncoupling of muscarinic M(3) and alpha(1B) adrenoceptors to Galpha(q/11) in SH-SY5Y human neuroblastoma cells.

作者信息

Bundey R A, Nahorski S R

机构信息

Department of Cell Physiology and Pharmacology, Medical Sciences Building, University of Leicester, Leicester, LE1 9HN.

出版信息

Br J Pharmacol. 2001 Sep;134(2):257-64. doi: 10.1038/sj.bjp.0704229.

Abstract
  1. The present study employed a [(35)S]-GTPgammaS binding protocol in conjunction with immunoprecipitation (IP) of the Galpha subunits to investigate the desensitization of G(q/11)-coupled receptors at the level of the G-protein activation. Membranes from SH-SY5Y cells expressing the recombinant human alpha(1B)-adrenoceptor (alpha(1B)-AR) (and endogenously expressing the M(3) muscarinic acetylcholine receptor (M(3)-AChR)) exhibited G(q/11) activation in a concentration-dependent manner in response to noradrenaline or methacholine. 2. Pre-treatment of intact cells with agonist prior to membrane preparation and use in the [(35)S]-GTPgammaS IP assay demonstrated that both receptors were homologously desensitized by pre-treatment with agonist since the G(q/11) activation in response to a secondary challenge with agonist was markedly reduced. Stimulation of alpha(1B)-AR was effective at heterologously desensitizing the M(3)-AChR. The PKC inhibitor, Ro-31-8220 (10 microM) was ineffective at preventing the agonist-mediated receptor desensitization. 3. [(32)P]P(i)-labelled cells allowed the detection of increases in receptor phosphorylation. Phorbol 12,13 dibutyrate (PDBu) (1 microM) was effective at producing a Ro-31-8220 (10 microM)-sensitive, detectable increase in alpha(1B)-AR but not M(3)-AChR phosphorylation. Noradrenaline (30 microM) stimulated alpha(1B)-AR phosphorylation, which could be partially inhibited by Ro-31-8220 (10 microM). The phosphorylation of M(3)-AChR was increased by methacholine (100 microM) incubation and this effect appeared to be insensitive to Ro-31-8220 (10 microM). 4. These findings demonstrate that [(35)S]-GTPgammaS-Galpha-subunit IP can be used to estimate receptor desensitization as a decline in receptor-G-protein coupling. Both the alpha(1B)-AR and M(3)-AChR undergo rapid homologous desensitization that is associated with an increase in receptor phosphorylation. The heterologous desensitization of M(3)-AChR produced by alpha(1B)-AR stimulation is not associated with a detectable increase in M(3)-AChR phosphorylation, suggesting that receptor phosphorylation is not necessarily a prerequisite for desensitization.
摘要
  1. 本研究采用[(35)S]-GTPγS结合实验方案并结合Gα亚基的免疫沉淀(IP),以研究G(q/11)偶联受体在G蛋白激活水平的脱敏作用。表达重组人α(1B)-肾上腺素能受体(α(1B)-AR)(并内源性表达M(3)毒蕈碱型乙酰胆碱受体(M(3)-AChR))的SH-SY5Y细胞的膜,对去甲肾上腺素或乙酰甲胆碱呈浓度依赖性地表现出G(q/11)激活。2. 在制备膜并用于[(35)S]-GTPγS IP分析之前,用激动剂预处理完整细胞,结果表明,用激动剂预处理后,两种受体均发生同源脱敏,因为对激动剂二次刺激的G(q/11)激活明显降低。刺激α(1B)-AR对M(3)-AChR的异源脱敏有效。蛋白激酶C抑制剂Ro-31-8220(10μM)不能有效阻止激动剂介导的受体脱敏。3. [(32)P]Pi标记的细胞可检测到受体磷酸化的增加。佛波醇12,13-二丁酸酯(PDBu)(1μM)可有效产生Ro-31-8220(10μM)敏感的、可检测到的α(1B)-AR磷酸化增加,但对M(3)-AChR磷酸化无作用。去甲肾上腺素(30μM)刺激α(1B)-AR磷酸化,Ro-31-8220(10μM)可部分抑制这种磷酸化。乙酰甲胆碱(100μM)孵育可增加M(3)-AChR的磷酸化,且这种作用似乎对Ro-31-8220(10μM)不敏感。4. 这些发现表明,[(35)S]-GTPγS-Gα亚基IP可用于评估受体脱敏,即受体-G蛋白偶联的下降。α(1B)-AR和M(3)-AChR均经历快速同源脱敏,这与受体磷酸化增加有关。α(1B)-AR刺激产生的M(3)-AChR异源脱敏与M(3)-AChR磷酸化的可检测增加无关,提示受体磷酸化不一定是脱敏的先决条件。

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