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陷窝、陷窝蛋白和陷窝相关蛋白:细胞信号和炎症的复杂调控。

Caveolae, caveolins, and cavins: complex control of cellular signalling and inflammation.

机构信息

Vascular Biology and Therapeutics Program, Department of Pharmacology, Yale University School of Medicine, Amistad Research Building, 10 Amistad Street, New Haven, CT 06520, USA.

出版信息

Cardiovasc Res. 2010 May 1;86(2):219-25. doi: 10.1093/cvr/cvq075. Epub 2010 Mar 3.

DOI:10.1093/cvr/cvq075
PMID:20202978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2856194/
Abstract

Caveolae are specialized lipid rafts that form flask-shaped invaginations of the plasma membrane. They are involved in cell signalling and transport and have been shown critically regulate vascular reactivity and blood pressure. The organization and functions of caveolae are mediated by coat proteins (caveolins) and support or adapter proteins (cavins). The caveolins, caveolin-1, -2, and -3, form the structural backbone of caveolae. These proteins are also highly integrated into caveolae function and have their own activity independent of caveolae. The cavins, cavins 1-4, are involved in regulation of caveolae and modulate the function of caveolins by promoting the membrane remodelling and trafficking of caveolin-derived structures. The relationships between these different proteins are complex and intersect with many aspects of cell function. Caveolae have also been implicated in chronic inflammatory conditions and other pathologies including atherosclerosis, inflammatory bowel disease, muscular dystrophy, and generalized dyslipidaemia. The pathogenic role of the caveolins is an emerging area, however, the roles of cavins in disease is just beginning to be explored. This review will examine the relationship between caveolins and cavins and explore the role of caveolae in inflammatory signalling mechanisms.

摘要

小窝是一种特殊的脂质筏,它们形成质膜的烧瓶状凹陷。它们参与细胞信号转导和运输,并且已经被证明可以严格调节血管反应性和血压。小窝的组织和功能由外套蛋白(小窝蛋白)和支持或衔接蛋白(小窝蛋白)介导。小窝蛋白,小窝蛋白-1、-2 和-3,构成小窝的结构骨架。这些蛋白质也高度整合到小窝的功能中,并且具有独立于小窝的自身活性。小窝蛋白,小窝蛋白 1-4,参与小窝的调节,并通过促进小窝蛋白衍生结构的膜重塑和运输来调节小窝蛋白的功能。这些不同蛋白质之间的关系非常复杂,并与细胞功能的许多方面相交。小窝也与慢性炎症状态和其他病理学有关,包括动脉粥样硬化、炎症性肠病、肌肉营养不良和全身性血脂异常。小窝蛋白的致病作用是一个新兴领域,然而,小窝蛋白在疾病中的作用才刚刚开始被探索。这篇综述将研究小窝蛋白和小窝蛋白之间的关系,并探讨小窝在炎症信号机制中的作用。

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本文引用的文献

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Endothelial [Ca2+]i and caveolin-1 antagonistically regulate eNOS activity and microvessel permeability in rat venules.内皮细胞 [Ca2+]i 和 caveolin-1 拮抗调节大鼠小静脉内皮型一氧化氮合酶活性和微血管通透性。
Cardiovasc Res. 2010 Jul 15;87(2):340-7. doi: 10.1093/cvr/cvq006. Epub 2010 Jan 15.
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Biogenesis of caveolae: stepwise assembly of large caveolin and cavin complexes.小窝的生物发生:大窖蛋白和窖质蛋白复合物的逐步组装。
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Caveolin-1 facilitates cyclooxygenase-2 protein degradation.窖蛋白-1 促进环氧化酶-2 蛋白降解。
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The platelet protein kinase C substrate pleckstrin binds directly to SDPR protein.血小板蛋白激酶 C 底物 pleckstrin 直接结合到 SDPR 蛋白上。
Platelets. 2009 Nov;20(7):446-57. doi: 10.3109/09537100903137314.
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Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy.人类PTRF突变导致小窝蛋白继发性缺乏,进而引发伴有全身性脂肪营养不良的肌肉萎缩症。
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The trafficking/interaction of eNOS and caveolin-1 induced by insulin modulates endothelial nitric oxide production.胰岛素诱导的内皮型一氧化氮合酶(eNOS)与小窝蛋白-1(caveolin-1)的转运/相互作用调节内皮一氧化氮的生成。
Mol Endocrinol. 2009 Oct;23(10):1613-23. doi: 10.1210/me.2009-0115. Epub 2009 Jul 16.
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Genetic evidence supporting a critical role of endothelial caveolin-1 during the progression of atherosclerosis.遗传证据支持内皮小窝蛋白-1在动脉粥样硬化进展过程中起关键作用。
Cell Metab. 2009 Jul;10(1):48-54. doi: 10.1016/j.cmet.2009.06.003.
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Rapid insulin-dependent endocytosis of the insulin receptor by caveolae in primary adipocytes.原代脂肪细胞中,小窝介导胰岛素受体的快速胰岛素依赖性内吞作用。
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