Insulin-like growth factor-1 signaling in cardiac aging

被引:47
|
作者
Lee, Wang-Soo [1 ]
Kim, Jaetaek [2 ]
机构
[1] Chung Ang Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul, South Korea
[2] Chung Ang Univ, Coll Med, Dept Internal Med, Div Endocrinol & Metab, Seoul, South Korea
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2018年 / 1864卷 / 05期
基金
新加坡国家研究基金会;
关键词
Aging; Insulin-like growth factor-1; Receptor; Heart; Longevity; PROSTATE-CANCER XENOGRAFTS; CORONARY-ARTERY-DISEASE; CHRONIC HEART-FAILURE; SMOOTH-MUSCLE-CELLS; APOE-DEFICIENT MICE; AMES DWARF MICE; IGF-I; CARDIOVASCULAR-DISEASE; OXIDATIVE STRESS; BINDING-PROTEINS;
D O I
10.1016/j.bbadis.2017.08.029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cardiovascular disease (CVD) is the leading cause of death in most developed countries. Aging is associated with enhanced risk of CVD. Insulin-like growth factor-1 (IGF-1) binds to its cognate receptor, IGF-1 receptor (IGF-1R), and exerts pleiotropic effects on cell growth, differentiation, development, and tissue repair. Importantly, IGF-1/IGF-1R signaling is implicated in cardiac aging and longevity. Cardiac aging is an intrinsic process that results in cardiac dysfunction, accompanied by molecular and cellular changes. In this review, we summarize the current state of knowledge regarding the link between the IGF-1/IGF-1R system and cardiac aging. The biological effects of IGF-1R and insulin receptor will be discussed and compared. Furthermore, we describe data regarding how deletion of IGF-1R in cardiomyocytes of aged knockout mice may delay the development of senescence-associated myocardial pathologies. This article is part of a Special issue entitled Cardiac adaptations to obesity, diabetes and insulin resistance, edited by Professors Jan F.C. Glatz, Jason R.B. Dyck and Christine Des Rosiers.
引用
收藏
页码:1931 / 1938
页数:8
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