The role of insulin/IGF-1 signaling in the longevity of model invertebrates, C. elegans and D. melanogaster

被引:183
作者
Altintas, Ozlem [1 ]
Park, Sangsoon [2 ]
Lee, Seung-Jae V. [1 ,2 ,3 ]
机构
[1] Pohang Univ Sci & Technol, Sch Interdisciplinary Biosci & Bioengn, Pohang 37673, South Korea
[2] Pohang Univ Sci & Technol, Dept Life Sci, Pohang 37673, South Korea
[3] Pohang Univ Sci & Technol, Informat Technol Convergence Engn, Pohang 37673, South Korea
基金
新加坡国家研究基金会;
关键词
Aging; C; elegans; D; melanogaster; Insulin/IGF-1; signaling; Longevity; BETA-AMYLOID PEPTIDE; EXTENDS LIFE-SPAN; AMYOTROPHIC-LATERAL-SCLEROSIS; SUPEROXIDE-DISMUTASE GENE; HEAT-SHOCK FACTOR; AGE-1; PI3; KINASE; CAENORHABDITIS-ELEGANS; OXIDATIVE-STRESS; REGULATES LONGEVITY; RECEPTOR HOMOLOG;
D O I
10.5483/BMBRep.2016.49.2.261
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Insulin/insulin-like growth factor (IGF)-1 signaling (IIS) pathway regulates aging in many organisms, ranging from simple invertebrates to mammals, including humans. Many seminal discoveries regarding the roles of IIS in aging and longevity have been made by using the roundworm Caenorhabditis elegans and the fruit fly Drosophila melanogaster. In this review, we describe the mechanisms by which various IIS components regulate aging in C. elegans and D. melanogaster. We also cover systemic and tissue-specific effects of the IIS components on the regulation of lifespan. We further discuss IIS-mediated physiological processes other than aging and their effects on human disease models focusing on C. elegans studies. As both C. elegans and D. melanogaster have been essential for key findings regarding the effects of IIS on organismal aging in general, these invertebrate models will continue to serve as workhorses to help our understanding of mammalian aging.
引用
收藏
页码:81 / 92
页数:12
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