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鞘氨醇激酶和1-磷酸鞘氨醇在调节内皮细胞生物学中的作用。

The role of sphingosine kinase and sphingosine-1-phosphate in the regulation of endothelial cell biology.

作者信息

Limaye Vidya

机构信息

Rheumatology Department, Royal Adelaide Hospital, Adelaide, Australia.

出版信息

Endothelium. 2008 May-Jun;15(3):101-12. doi: 10.1080/10623320802125342.

Abstract

Sphingolipids, in particular sphingosine kinase (SphK) and its product sphingosine-1-phosphate (S1P), are now recognized to play an important role in regulating many critical processes in endothelial cells. Activation of SphK1 is essential in mediating the endothelial proinflammatory effects of inflammatory cytokines such as tumor necrosis factor (TNF). In addition, S1P regulates the survival and proliferation of endothelial cells, as well as their ability to undergo cell migration, all essential components of angiogenesis. Thus the inflammatory and angiogenic potential of the endothelium is in part regulated by intracellular components including the activity of SphK1 and levels of S1P. Herein a review of the sphingomyelin pathway with a particular focus on its relevance to endothelial cell biology is presented.

摘要

鞘脂,尤其是鞘氨醇激酶(SphK)及其产物鞘氨醇-1-磷酸(S1P),目前被认为在调节内皮细胞的许多关键过程中发挥重要作用。SphK1的激活对于介导炎性细胞因子(如肿瘤坏死因子(TNF))的内皮促炎作用至关重要。此外,S1P调节内皮细胞的存活和增殖,以及它们进行细胞迁移的能力,而这些都是血管生成的所有重要组成部分。因此,内皮细胞的炎症和血管生成潜能部分受包括SphK1活性和S1P水平在内的细胞内成分调节。本文对鞘磷脂途径进行综述,特别关注其与内皮细胞生物学的相关性。

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