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The biology of beta-adrenergic receptors: analysis in human epidermoid carcinoma A431 cells.

作者信息

Wang H Y, Berrios M, Hadcock J R, Malbon C C

机构信息

Department of Biochemistry, National Defence Medical Center, Taipei, Taiwan, Republic of China.

出版信息

Int J Biochem. 1991;23(1):7-20. doi: 10.1016/0020-711x(91)90003-6.

DOI:10.1016/0020-711x(91)90003-6
PMID:1850702
Abstract
  1. G-protein-linked transmembrane signaling has emerged as a major pathway for information transduction across the cell membrane. 2. In addition to photopigments that propagate the signal from light, cell-surface receptors for hormones, neurotransmitters, and autacoids propagate signals from ligand binding to membrane-bound effector units via G-proteins. 3. Biochemical and molecular features of one prominent member of these receptors, the beta-adrenergic receptor, will be highlighted in the present article. 4. The role of the human epidermoid carcinoma A431 cells as a model for the study of the structure and biology of beta-adrenergic receptors will be emphasized. 5. A model for receptor regulation, gleaned from recent advances in the biochemistry, cell and molecular biology of beta-adrenergic receptors, is discussed.
摘要

相似文献

1
The biology of beta-adrenergic receptors: analysis in human epidermoid carcinoma A431 cells.
Int J Biochem. 1991;23(1):7-20. doi: 10.1016/0020-711x(91)90003-6.
2
Beta-adrenergic receptor regulation. New insights on biochemical and molecular mechanisms.β-肾上腺素能受体调节。关于生化和分子机制的新见解。
Receptor. 1990;1(1-2):13-32.
3
Mapping the functional domains of the beta-adrenergic receptor.
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Drug Des Discov. 1993;9(3-4):199-211.
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Indirect immunofluorescence localization of beta-adrenergic receptors and G-proteins in human A431 cells.人A431细胞中β-肾上腺素能受体和G蛋白的间接免疫荧光定位
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Determination of structural domains for G protein coupling and ligand binding in beta 3-adrenergic receptor.β3肾上腺素能受体中G蛋白偶联和配体结合结构域的确定。
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Separation of the structural requirements for agonist-promoted activation and sequestration of the beta-adrenergic receptor.β-肾上腺素能受体激动剂促进激活和隔离的结构要求的分离。
Mol Pharmacol. 1990 Jun;37(6):775-9.
8
From ligand binding to gene expression: new insights into the regulation of G-protein-coupled receptors.从配体结合到基因表达:对G蛋白偶联受体调控的新见解
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Phorbol-ester-induced phosphorylation of the beta 2-adrenergic receptor decreases its coupling to Gs.佛波酯诱导的β2-肾上腺素能受体磷酸化降低了其与Gs的偶联。
FEBS Lett. 1991 Feb 25;279(2):243-8. doi: 10.1016/0014-5793(91)80159-z.
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Comparative rates of desensitization of beta-adrenergic receptors by the beta-adrenergic receptor kinase and the cyclic AMP-dependent protein kinase.β-肾上腺素能受体激酶和环磷酸腺苷依赖性蛋白激酶对β-肾上腺素能受体的脱敏比较率。
Proc Natl Acad Sci U S A. 1991 Jul 15;88(14):6201-4. doi: 10.1073/pnas.88.14.6201.

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J Mol Signal. 2012 May 14;7(1):4. doi: 10.1186/1750-2187-7-4.
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AKAP12 and AKAP5 form higher-order hetero-oligomers.A激酶锚定蛋白12(AKAP12)和A激酶锚定蛋白5(AKAP5)形成高阶异源寡聚体。
J Mol Signal. 2011 Aug 10;6:8. doi: 10.1186/1750-2187-6-8.
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AKAP5 and AKAP12 Form Homo-oligomers.A激酶锚定蛋白5(AKAP5)和A激酶锚定蛋白12(AKAP12)形成同型寡聚体。
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G-protein-coupled receptor-associated A-kinase anchoring proteins AKAP5 and AKAP12: differential signaling to MAPK and GPCR recycling.G蛋白偶联受体相关的A激酶锚定蛋白AKAP5和AKAP12:对丝裂原活化蛋白激酶和G蛋白偶联受体循环的差异信号传导
J Mol Signal. 2008 Dec 2;3:19. doi: 10.1186/1750-2187-3-19.
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pp60Src mediates insulin-stimulated sequestration of the beta(2)-adrenergic receptor: insulin stimulates pp60Src phosphorylation and activation.pp60Src介导胰岛素刺激的β₂-肾上腺素能受体隔离:胰岛素刺激pp60Src磷酸化和激活。
Mol Biol Cell. 2002 Nov;13(11):3943-54. doi: 10.1091/mbc.e02-03-0174.
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Lipolytic catecholamine resistance due to decreased beta 2-adrenoceptor expression in fat cells.脂肪细胞中β2-肾上腺素能受体表达降低导致脂解性儿茶酚胺抵抗。
J Clin Invest. 1992 Dec;90(6):2175-86. doi: 10.1172/JCI116103.