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鞘氨醇 1-磷酸在肝脏健康和疾病中的不同作用。

Divergent Role of Sphingosine 1-Phosphate in Liver Health and Disease.

机构信息

Department of Toxicology, Institute of Nutritional Science, Faculty of Mathematics and Natural Science, University of Potsdam, Arthur-Scheunert Allee 114-116, 14558 Nuthetal, Germany.

出版信息

Int J Mol Sci. 2018 Mar 3;19(3):722. doi: 10.3390/ijms19030722.

Abstract

Two decades ago, sphingosine 1-phosphate (S1P) was discovered as a novel bioactive molecule that regulates a variety of cellular functions. The plethora of S1P-mediated effects is due to the fact that the sphingolipid not only modulates intracellular functions but also acts as a ligand of G protein-coupled receptors after secretion into the extracellular environment. In the plasma, S1P is found in high concentrations, modulating immune cell trafficking and vascular endothelial integrity. The liver is engaged in modulating the plasma S1P content, as it produces apolipoprotein M, which is a chaperone for the S1P transport. Moreover, the liver plays a substantial role in glucose and lipid homeostasis. A dysfunction of glucose and lipid metabolism is connected with the development of liver diseases such as hepatic insulin resistance, non-alcoholic fatty liver disease, or liver fibrosis. Recent studies indicate that S1P is involved in liver pathophysiology and contributes to the development of liver diseases. In this review, the current state of knowledge about S1P and its signaling in the liver is summarized with a specific focus on the dysregulation of S1P signaling in obesity-mediated liver diseases. Thus, the modulation of S1P signaling can be considered as a potential therapeutic target for the treatment of hepatic diseases.

摘要

二十年前,鞘氨醇 1-磷酸(S1P)被发现是一种新型的生物活性分子,可调节多种细胞功能。鞘氨醇不仅调节细胞内功能,而且在分泌到细胞外环境后作为 G 蛋白偶联受体的配体发挥作用,这使得 S1P 介导的作用多种多样。在血浆中,S1P 浓度较高,可调节免疫细胞的迁移和血管内皮的完整性。肝脏参与调节血浆 S1P 含量,因为它产生载脂蛋白 M,后者是 S1P 转运的伴侣。此外,肝脏在葡萄糖和脂质稳态中起着重要作用。葡萄糖和脂质代谢功能障碍与肝脏疾病的发展有关,如肝胰岛素抵抗、非酒精性脂肪性肝病或肝纤维化。最近的研究表明,S1P 参与肝脏病理生理学,并有助于肝脏疾病的发展。在这篇综述中,总结了 S1P 及其在肝脏中的信号转导的最新知识,特别关注肥胖介导的肝脏疾病中 S1P 信号转导的失调。因此,S1P 信号转导的调节可以被认为是治疗肝脏疾病的潜在治疗靶点。

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