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成纤维细胞生长因子23(FGF23)与α-klotho信号通路的研究进展

Update on FGF23 and Klotho signaling.

作者信息

Erben Reinhold G

机构信息

University of Veterinary Medicine Vienna, Vienna, Austria.

出版信息

Mol Cell Endocrinol. 2016 Sep 5;432:56-65. doi: 10.1016/j.mce.2016.05.008. Epub 2016 May 10.

Abstract

Fibroblast growth factor-23 (FGF23) is a bone-derived hormone known to suppress phosphate reabsorption and vitamin D hormone production in the kidney. Klotho was originally discovered as an anti-aging factor, but the functional role of Klotho is still a controversial issue. Three major functions have been proposed, a hormonal function of soluble Klotho, an enzymatic function as glycosidase, and the function as an obligatory co-receptor for FGF23 signaling. The purpose of this review is to highlight the recent advances in the area of FGF23 and Klotho signaling in the kidney, in the parathyroid gland, in the cardiovascular system, in bone, and in the central nervous system. During recent years, major new functions of FGF23 and Klotho have been discovered in these organ systems. Based on these novel findings, FGF23 has emerged as a pleiotropic endocrine and auto-/paracrine factor influencing not only mineral metabolism but also cardiovascular function.

摘要

成纤维细胞生长因子23(FGF23)是一种骨源性激素,已知其可抑制肾脏中的磷酸盐重吸收和维生素D激素生成。Klotho最初被发现是一种抗衰老因子,但其功能作用仍是一个有争议的问题。目前已提出了三种主要功能,即可溶性Klotho的激素功能、作为糖苷酶的酶功能以及作为FGF23信号传导的必需共受体的功能。本综述的目的是强调肾脏、甲状旁腺、心血管系统、骨骼和中枢神经系统中FGF23和Klotho信号传导领域的最新进展。近年来,在这些器官系统中发现了FGF23和Klotho的主要新功能。基于这些新发现,FGF23已成为一种多效性内分泌和自分泌/旁分泌因子,不仅影响矿物质代谢,还影响心血管功能。

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