Suppr超能文献

小窝蛋白-1与小窝在动脉粥样硬化中的作用:在脂纹形成和内膜增生中的不同作用

Caveolin-1 and caveolae in atherosclerosis: differential roles in fatty streak formation and neointimal hyperplasia.

作者信息

Frank Philippe G, Lisanti Michael P

机构信息

Department of Molecular Pharmacology and the Albert Einstein Diabetes Research and Training Center (DRTC), and Department of Urology, Albert Einstein College of Medicine, The Bronx, New York 10461, USA.

出版信息

Curr Opin Lipidol. 2004 Oct;15(5):523-9. doi: 10.1097/00041433-200410000-00005.

Abstract

PURPOSE OF REVIEW

Caveolae are 50-100 nm cell surface plasma membrane invaginations observed in terminally differentiated cells. They are characterized by the presence of the protein marker caveolin-1. Caveolae and caveolin-1 are present in almost every cell type that has been implicated in the development of an atheroma. These include endothelial cells, macrophages, and smooth muscle cells. Caveolae and caveolin-1 are involved in regulating several signal transduction pathways and processes that play an important role in atherosclerosis.

RECENT FINDINGS

Several recent studies using genetically engineered mice (Cav-1 (-/-) null animals) have now clearly demonstrated a role for caveolin-1 and caveolae in the development of atherosclerosis. In fact, they suggest a rather complex one, either proatherogenic or antiatherogenic, depending on the cell type examined. For example, in endothelial cells, caveolin-1 and caveolae may play a proatherogenic role by promoting the transcytosis of LDL-cholesterol particles from the blood to the sub-endothelial space. In contrast, in smooth muscle cells, the ability of caveolin-1 to negatively regulate cell proliferation (neointimal hyperplasia) may have an antiatherogenic effect.

SUMMARY

Caveolin-1 and caveolae play an important role in several steps involved in the initiation of an atheroma. Development of new drugs that regulate caveolin-1 expression may be important in the prevention or treatment of atherosclerotic vascular disease.

摘要

综述目的

小窝是在终末分化细胞中观察到的50 - 100纳米的细胞表面质膜内陷结构。它们的特征是存在蛋白质标记物小窝蛋白-1。小窝和小窝蛋白-1几乎存在于与动脉粥样硬化发展相关的每一种细胞类型中。这些细胞包括内皮细胞、巨噬细胞和平滑肌细胞。小窝和小窝蛋白-1参与调节几种在动脉粥样硬化中起重要作用的信号转导途径和过程。

最新发现

最近几项使用基因工程小鼠(Cav-1 (-/-)基因敲除动物)的研究现已清楚地证明了小窝蛋白-1和小窝在动脉粥样硬化发展中的作用。事实上,它们表明了一种相当复杂的作用,根据所研究的细胞类型,既可能是促动脉粥样硬化的,也可能是抗动脉粥样硬化的。例如,在内皮细胞中,小窝蛋白-1和小窝可能通过促进低密度脂蛋白胆固醇颗粒从血液向内膜下间隙的转胞吞作用而发挥促动脉粥样硬化作用。相反,在平滑肌细胞中,小窝蛋白-1负向调节细胞增殖(内膜增生)的能力可能具有抗动脉粥样硬化作用。

总结

小窝蛋白-1和小窝在动脉粥样硬化起始的几个步骤中起重要作用。开发调节小窝蛋白-1表达的新药可能对预防或治疗动脉粥样硬化性血管疾病具有重要意义。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验