鞘氨醇-1-磷酸代谢的结构生物学初探。

Ruobing Ren, Bin Pang, Yufei Han, Yihao Li
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引用次数: 2

摘要

鞘鞘醇-1-磷酸(S1P)是鞘脂代谢的关键代谢物,在血管和免疫系统中起着重要作用。它调节血管生成、血管完整性和稳态、过敏反应和淋巴细胞运输。S1P与鞘氨醇相互转化,鞘氨醇也来源于神经酰胺的去酰化。细胞中S1P的水平和与神经酰胺的比例受到其代谢途径的严格调节。异常的S1P生成导致许多严重疾病的发生和发展,如代谢综合征、癌症、多发性硬化症等自身免疫性疾病、肾脏和心血管疾病。近年来,对S1P代谢途径结构的研究取得了巨大进展。本文通过对鞘氨醇激酶、S1P转运体和S1P受体的结构和生化研究,以及针对S1P信号的治疗方法的研究,对S1P的代谢进行了综述。本文综述的研究进展为进一步探索S1P的功能提供了新的视角,并有助于开发靶向S1P信号的治疗分子,提高特异性和治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Glimpse of the Structural Biology of the Metabolism of Sphingosine-1-Phosphate.

A Glimpse of the Structural Biology of the Metabolism of Sphingosine-1-Phosphate.

A Glimpse of the Structural Biology of the Metabolism of Sphingosine-1-Phosphate.

A Glimpse of the Structural Biology of the Metabolism of Sphingosine-1-Phosphate.

As a key sphingolipid metabolite, sphingosine-1-phosphate (S1P) plays crucial roles in vascular and immune systems. It regulates angiogenesis, vascular integrity and homeostasis, allergic responses, and lymphocyte trafficking. S1P is interconverted with sphingosine, which is also derived from the deacylation of ceramide. S1P levels and the ratio to ceramide in cells are tightly regulated by its metabolic pathways. Abnormal S1P production causes the occurrence and progression of numerous severe diseases, such as metabolic syndrome, cancers, autoimmune disorders such as multiple sclerosis, and kidney and cardiovascular diseases. In recent years, huge advances on the structure of S1P metabolic pathways have been accomplished. In this review, we have got a glimpse of S1P metabolism through structural and biochemical studies of: sphingosine kinases, S1P transporters and S1P receptors, and the development of therapeutics targeting S1P signaling. The progress we summarize here could provide fresh perspectives to further the exploration of S1P functions and facilitate the development of therapeutic molecules targeting S1P signaling with improved specificity and therapeutic effects.

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