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FGF23-klotho系统缺陷导致加速衰老的分子机制

Molecular Mechanisms Underlying Accelerated Aging by Defects in the FGF23-Klotho System.

作者信息

Kuro-O Makoto

机构信息

Division of Anti-Aging Medicine, Center for Molecular Medicine, Jichi Medical University, 3311-1 Yakushiji, Shimotsuke, Tochigi 329-0498, Japan.

Department of Internal Medicine, Division of Mineral Metabolism, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9072, USA.

出版信息

Int J Nephrol. 2018 May 21;2018:9679841. doi: 10.1155/2018/9679841. eCollection 2018.

Abstract

The basic research of aging has been primarily focused on elucidating mechanisms of aging and longevity that are evolutionarily conserved from yeasts to primates. Such efforts have culminated in the notion that (1) senescence at the cellular level is associated with aging at the organismal level and that (2) calorie restriction and growth suppression decelerate aging. However, these important findings in the basic research have not necessarily been linked to improvement of daily medical practice in the aging society. It has become increasingly important to investigate mechanisms of aging unique to mammals or humans and apply the research fruits for the treatment of major age-related disorders to extend the health span. Seminal studies on the mouse, a mutant exhibiting a premature aging syndrome, have identified phosphate as a proaging factor in mammals. In this review, mechanisms of phosphate-induced premature aging and potential therapeutic targets will be discussed, which may be directly applicable for developing novel strategies for the treatment of chronic kidney disease and its complications.

摘要

衰老的基础研究主要集中在阐明从酵母到灵长类动物进化上保守的衰老和长寿机制。这些努力最终形成了这样的观念:(1)细胞水平的衰老与机体水平的衰老相关,以及(2)热量限制和生长抑制会减缓衰老。然而,基础研究中的这些重要发现不一定与老龄化社会日常医疗实践的改善相关联。研究哺乳动物或人类特有的衰老机制,并将研究成果应用于治疗主要的年龄相关疾病以延长健康寿命,变得越来越重要。对一种表现出早衰综合征的突变小鼠的开创性研究已经确定磷酸盐是哺乳动物中的一种促衰老因子。在这篇综述中,将讨论磷酸盐诱导早衰的机制和潜在的治疗靶点,这些可能直接适用于开发治疗慢性肾病及其并发症的新策略。

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