The starvation hormone, fibroblast growth factor-21, extends lifespan in mice

被引:279
作者
Zhang, Yuan [1 ]
Xie, Yang [2 ]
Berglund, Eric D. [3 ]
Coate, Katie Colbert [4 ]
He, Tian Teng [5 ]
Katafuchi, Takeshi [1 ]
Xiao, Guanghua [2 ]
Potthoff, Matthew J. [4 ]
Wei, Wei [1 ]
Wan, Yihong [1 ]
Yu, Ruth T. [6 ]
Evans, Ronald M. [6 ]
Kliewer, Steven A. [1 ,7 ]
Mangelsdorf, David J. [4 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Pharmacol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Clin Sci, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dallas, TX 75390 USA
[4] Univ Texas SW Med Ctr Dallas, Howard Hughes Med Inst, Dept Pharmacol, Dallas, TX 75390 USA
[5] Univ Texas SW Med Ctr Dallas, Adv Imaging Res Ctr, Dallas, TX 75390 USA
[6] Salk Inst Biol Studies, Howard Hughes Med Inst, Gene Express Lab, San Diego, CA USA
[7] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
FACTOR; 21; FGF21; DWARF MICE; GENE; LONGEVITY; DIET; FAT;
D O I
10.7554/eLife.00065
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
Fibroblast growth factor-21 (FGF21) is a hormone secreted by the liver during fasting that elicits diverse aspects of the adaptive starvation response. Among its effects, FGF21 induces hepatic fatty acid oxidation and ketogenesis, increases insulin sensitivity, blocks somatic growth and causes bone loss. Here we show that transgenic overexpression of FGF21 markedly extends lifespan in mice without reducing food intake or affecting markers of NAD+ metabolism or AMP kinase and mTOR signaling. Transcriptomic analysis suggests that FGF21 acts primarily by blunting the growth hormone/insulin-like growth factor-1 signaling pathway in liver. These findings raise the possibility that FGF21 can be used to extend lifespan in other species.
引用
收藏
页数:14
相关论文
共 38 条
[1]
[Anonymous], 2003, Modelling Survival Data in Medical Research
[2]
Considerations in the design of hyperinsulinemic-euglycemic clamps in the conscious mouse [J].
Ayala, JE ;
Bracy, DP ;
McGuinness, OP ;
Wasserman, DH .
DIABETES, 2006, 55 (02) :390-397
[3]
GH-Dependent STAT5 Signaling Plays an Important Role in Hepatic Lipid Metabolism [J].
Barclay, Johanna L. ;
Nelson, Caroline N. ;
Ishikawa, Mayumi ;
Murray, Lauren A. ;
Kerr, Linda M. ;
McPhee, Timothy R. ;
Powell, Elizabeth E. ;
Waters, Michael J. .
ENDOCRINOLOGY, 2011, 152 (01) :181-192
[4]
Life extension in the dwarf mouse [J].
Bartke, A ;
Brown-Borg, H .
CURRENT TOPICS IN DEVELOPMENTAL BIOLOGY, VOL 63, 2004, 63 :189-+
[5]
The Critical Role of Metabolic Pathways in Aging [J].
Barzilai, Nir ;
Huffman, Derek M. ;
Muzumdar, Radhika H. ;
Bartke, Andrzej .
DIABETES, 2012, 61 (06) :1315-1322
[6]
Fibroblast Growth Factor 21 Controls Glycemia via Regulation of Hepatic Glucose Flux and Insulin Sensitivity [J].
Berglund, Eric D. ;
Li, Candice Y. ;
Bina, Holly A. ;
Lynes, Sara E. ;
Michael, M. Dodson ;
Shanafelt, Armen B. ;
Kharitonenkov, Alexei ;
Wasserman, David H. .
ENDOCRINOLOGY, 2009, 150 (09) :4084-4093
[7]
Genetic links between diet and lifespan: shared mechanisms from yeast to humans [J].
Bishop, Nicholas A. ;
Guarente, Leonard .
NATURE REVIEWS GENETICS, 2007, 8 (11) :835-844
[8]
GH and IGF1: Roles in Energy Metabolism of Long-Living GH Mutant Mice [J].
Brown-Borg, Holly M. ;
Bartke, Andrzej .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2012, 67 (06) :652-660
[9]
Dwarf mice and the ageing process [J].
BrownBorg, HM ;
Borg, KE ;
Meliska, CJ ;
Bartke, A .
NATURE, 1996, 384 (6604) :33-33
[10]
Growth Hormone Induces Hepatic Production of Fibroblast Growth Factor 21 through a Mechanism Dependent on Lipolysis in Adipocytes [J].
Chen, Wei ;
Hoo, Ruby Lai-chong ;
Konishi, Morichika ;
Itoh, Nobuyuki ;
Lee, Pui-chi ;
Ye, Hong-ying ;
Lam, Karen Siu-ling ;
Xu, Aimin .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (40) :34559-34566