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综述: 人类早衰症的发病机制及干预方法
引用本文:王泽华,李洪宇,曲静,张维绮,刘光慧.综述: 人类早衰症的发病机制及干预方法[J].生物化学与生物物理进展,2018,45(9):926-934.
作者姓名:王泽华  李洪宇  曲静  张维绮  刘光慧
作者单位:中国科学院动物研究所干细胞与生殖生物学国家重点实验室;中国科学院生物物理研究所生物大分子国家重点实验室;中国科学院干细胞与再生创新研究院
基金项目:中国科学院战略性先导科技专项 (XDA16010100),国家重点基础研究发展计划 (973)(2015CB964800,2017YFA0103304, 2017YFA0102802,2014CB910503,2014CB964600,2018YFA0107203),国家自然科学基金(91749202,31471394, 31671429,91749123,81625009,81330008,81371342,81471414,81422017,81601233,81671377,31601109,31601158,81771515,81701388,31571533,31621004,81822018)资助项目
摘    要:衰老是一种在细胞和组织水平逐渐发生功能衰退的过程.早衰症是一类罕见的人类遗传性疾病,以加速衰老为特征.对早衰症的研究有助于理解人类衰老的生理过程,对衰老相关疾病的防治具有借鉴意义.成人早衰症和儿童早衰症是两种著名的人类早衰症,本文将综述这两种早衰症的发病机制及干预方法.

关 键 词:人类,早衰,成人早衰症,儿童早衰症,机制,干预
收稿时间:2018/7/17 0:00:00
修稿时间:2018/7/17 0:00:00

Review: Premature Aging Disorders: Mechanisms and Potential Therapeutic Interventions
WANG Ze-Hu,LI Hong-Yu,QU Jing,ZHANG Wei-Qi and LIU Guang-Hui.Review: Premature Aging Disorders: Mechanisms and Potential Therapeutic Interventions[J].Progress In Biochemistry and Biophysics,2018,45(9):926-934.
Authors:WANG Ze-Hu  LI Hong-Yu  QU Jing  ZHANG Wei-Qi and LIU Guang-Hui
Institution:State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China,National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China,State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China; Institute of Stem cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China,National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China; Institute of Stem cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China and National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China; Institute of Stem cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China
Abstract:Aging is a process of gradual functional deterioration at the cellular and organismal level. Progeroid syndromes represent a group of rare genetic disorders with features of premature aging. Werner syndrome (WS) and Hutchinson-Gilford progeria syndrome (HGPS) are two of the best characterized human progeroid syndromes. The study of premature aging is helpful to understand the physiological processes of human aging and is useful for the prevention and treatment of aging-related diseases. This review focuses on the mechanisms and potential therapeutic interventions of these two progeroid diseases.
Keywords:human  premature aging  progeroid syndrome  WS  HGPS  mechanism
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