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肝纤维化进程中细胞衰老的作用及相关机制的研究进展
引用本文:孔德松,魏东华,张峰,张自力,陆茵,王爱云,陈文星,郑仕中.肝纤维化进程中细胞衰老的作用及相关机制的研究进展[J].中国药理学与毒理学杂志,2012,26(5):688-691.
作者姓名:孔德松  魏东华  张峰  张自力  陆茵  王爱云  陈文星  郑仕中
作者单位:1. 南京中医药大学中药学一级学科,江苏南京,210029
2. 哈尔滨医科大学大庆校区药学院中药学与药用植物学系,黑龙江大庆,163319
3. 南京中医药大学中药学一级学科,江苏南京210029;南京中医药大学江苏省中药药效与安全性评价重点实验室,江苏南京210046
基金项目:国家自然科学基金,国家自然科学基金,江苏省自然科学基金,教育部博士点博导基金,江苏省针灸学重点实验室开放课题,江苏省六大人才基金,江苏高校优势学科建设工程资助项目,十一五科技支撑计划,南京中医药大学中药学一级学科开放课题
摘    要:细胞衰老是指细胞脱离细胞周期并不可逆地丧失增殖能力后进入的一种相对稳定的状态,是细胞生命活动的一种客观规律。细胞衰老与肝纤维化的发生与发展存在密切关系。肝星状细胞的大量活化、增殖和肝细胞的凋亡是肝纤维化病理进程中的关键事件,促进肝星状细胞的衰老可阻断其活化从而实现抗肝纤维化的效果;肝细胞与胆管上皮细胞等各类型细胞的衰老在肝纤维化进程中也有重要作用。本文针对细胞衰老与肝纤维化的关系及其分子机制的研究进展进行了综述。

关 键 词:细胞衰老  肝硬化  肝细胞  细胞增殖  细胞凋亡
收稿时间:2011-9-5
修稿时间:2011-12-16

Progress in roles and mechanisms of cellular senescence in hepatic fibrogenesis
KONG De-song , WEI Dong-hua , ZHANG Feng , ZHANG Zi-li , LU Yin , WANG Ai-yun , CHEN Wen-xing , ZHENG Shi-zhong.Progress in roles and mechanisms of cellular senescence in hepatic fibrogenesis[J].Chinese Journal of Pharmacology and Toxicology,2012,26(5):688-691.
Authors:KONG De-song  WEI Dong-hua  ZHANG Feng  ZHANG Zi-li  LU Yin  WANG Ai-yun  CHEN Wen-xing  ZHENG Shi-zhong
Institution:1. National First-Class Key Discipline for Traditional Chinese Medicine, Nanning University of Chinese Medicine, Nanjing 210046, China;2. Department of Chinese Materia Medica and Pharmaceutical Botany, College of Pharmacy, Daqing Branch of Harbin Medical University, Daqing 163319, China;3. Jiangsu Key Laboratory for Pharmacology and Safety Evaluation of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing 210046, China
Abstract:Cellular senescence is defined as departure of cell cycle and entrance into a relatively stable state with an irreversible loss of proliferative capacity. It is a common process of cell life. Cell senescence has a close relationship with hepatic fibrosis. Activation of hepatic stellate cells and apoptosis of hepatocytes has been considered a key event in hepatic fibrogenesis. Recently, it has been proposed that cell senescence can block hepatic stellate cell activation and generate antifibrotic effects. Moreover, senescence of cell types including hepatocytes and bile duct epithelial cells also plays a role in hepatic fibrosis. This review focuses on the associations between cell senescence and hepatic fibrosis and molecular mechanisms.
Keywords:cell aging  hepatic cirrohosis  hepatocytes  cell proliferation  apoptosis
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