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M1毒蕈碱型乙酰胆碱受体与β2-肾上腺素能受体之间的相互作用。环磷酸腺苷(cAMP)和M1毒蕈碱型受体的第三个细胞内环赋予异源调节作用。

Cross-talk between m1 muscarinic acetylcholine and beta 2-adrenergic receptors. cAMP and the third intracellular loop of m1 muscarinic receptors confer heterologous regulation.

作者信息

Lee N H, Fraser C M

机构信息

Section on Molecular Neurobiology, National Institute on Alcohol Abuse and Alcoholism, Rockville, Maryland 20852.

出版信息

J Biol Chem. 1993 Apr 15;268(11):7949-57.

PMID:8385129
Abstract

Genes encoding the m1 muscarinic (m1 mAChR) and beta 2-adrenergic receptors (beta 2AR) were stably co-expressed into Chinese hamster ovary (CHO) cells to study receptor regulation and cross-talk. Persistent activation of the beta 2AR/adenylate cyclase pathway by isoproterenol leads to heterologous desensitization, internalization, and down-regulation of the m1 mAChR which is comparable, but smaller in magnitude, with that seen with persistent activation of the m1 mAChR by carbachol. This heterologous effect was mimicked by dibutyryl cAMP and forskolin and antagonized by the protein kinase A (PKA) inhibitor H-8. A potential consensus sequence for phosphorylation by PKA (Lys351-Arg-Lys-Thr354) exists on the third intracellular loop of the m1 mAChR, suggesting that receptor phosphorylation by PKA may be involved in heterologous regulation. The loss of m1 mAChRs induced by carbachol was not reversed by H-8, indicating that homologous regulation is not dependent on PKA. Recent evidence suggests that muscarinic agonist-mediated internalization of the m1 mAChR involves the third intracellular loop (i3) (Maeda, S., Lameh, J., Mallet, W. G., Philip, M., Ramachandran, J., and Sadee, W. (1990) FEBS Lett. 269, 386-388). Three deletion mutant receptors were constructed in which the majority, or small regions, of i3 were eliminated but the membrane proximal portions of the loop were left intact. Each of the mutants was co-expressed with the beta 2AR in CHO cells. A small region in i3 was identified which is crucial for carbachol- and isoproterenol-promoted internalization and down-regulation. This region contains a series of 6 serine residues within an 8-amino acid stretch. A similar domain has been identified in the carboxyl tail of the beta 2AR and has been proposed to participate in receptor internalization (Hausdorff, W. P., Campbell, P. T., Ostrowski, J., Yu, S. S., Caron, M. G., and Lefkowitz, R. J. (1991) Proc. Natl. Acad. Sci. U.S.A. 88, 2979-2983).

摘要

将编码毒蕈碱型 m1 受体(m1 mAChR)和β2 - 肾上腺素能受体(β2AR)的基因稳定共表达于中国仓鼠卵巢(CHO)细胞中,以研究受体调节和相互作用。异丙肾上腺素对β2AR/腺苷酸环化酶途径的持续激活导致 m1 mAChR 的异源脱敏、内化和下调,这与卡巴胆碱对 m1 mAChR 的持续激活所导致的情况相当,但程度较小。这种异源效应可被二丁酰 cAMP 和福斯可林模拟,并被蛋白激酶 A(PKA)抑制剂 H - 8 拮抗。在 m1 mAChR 的第三个细胞内环上存在一个潜在的 PKA 磷酸化共有序列(Lys351 - Arg - Lys - Thr354),这表明 PKA 介导的受体磷酸化可能参与异源调节。H - 8 不能逆转卡巴胆碱诱导的 m1 mAChRs 的丢失,表明同源调节不依赖于 PKA。最近的证据表明,毒蕈碱激动剂介导的 m1 mAChR 内化涉及第三个细胞内环(i3)(前田,S.,拉梅,J.,马利特,W. G.,菲利普,M.,拉马钱德兰,J.,和萨迪,W.(1990)《欧洲生物化学学会联合会快报》269,386 - 388)。构建了三个缺失突变受体,其中大部分或小区域的 i3 被去除,但环的膜近端部分保持完整。每个突变体都与β2AR 在 CHO 细胞中共表达。在 i3 中鉴定出一个小区域,它对卡巴胆碱和异丙肾上腺素促进的内化和下调至关重要。该区域在一个 8 个氨基酸的片段内包含一系列 6 个丝氨酸残基。在β2AR 的羧基末端也鉴定出了类似的结构域,并被认为参与受体内化(豪斯多夫,W. P.,坎贝尔,P. T.奥斯特罗夫斯基,J.,于,S. S.,卡龙,M. G.,和莱夫科维茨,R. J.(1991)《美国国家科学院院刊》88,2979 - 2983)。

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