Regulation of multiple ageing-like phenotypes by inducible klotho gene expression in klotho mutant mice

被引:112
作者
Masuda, H
Chikuda, H
Suga, T
Kawaguchi, H
Kuro-o, M
机构
[1] Univ Texas, SW Med Ctr, Dept Pathol, Dallas, TX 75390 USA
[2] Gunma Univ, Sch Med, Dept Internal Med 2, Maebashi, Gumma 3718511, Japan
[3] Univ Tokyo, Dept Sensory & Motor Syst Med, Tokyo 1138655, Japan
基金
美国国家卫生研究院;
关键词
klotho; transgenic mice; ageing;
D O I
10.1016/j.mad.2005.07.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mice carrying a loss-of-function mutation in the klotho gene (KL-/- mice) develop ageing-like symptoms around 4 weeks after birth and suffer from multiple age-related disorders observed in humans, including osteoporosis, arteriosclerosis, and pulmonary emphysema. The klotho gene encodes a single-pass transmembrane protein that may function in signaling pathways that suppress ageing. To investigate the ability of Klotho to regulate the development of ageing-related disorders, we established an inducible Klotho expression system using KL-/- mice carrying an exogenous klotho gene fused to the mouse metallothionein-I promoter, in which Klotho expression was dependent on zinc water feeding. We demonstrate that many advanced ageing-like KL-/- phenotypes were restored to normal whenever Klotho expression was induced. Conversely, decreasing Klotho expression in these rescued KL-/- mice induced several ageing-like KL-/- phenotypes. Our data indicate that Klotho may be effective in the treatment of multiple age-related disorders and is essential for maintaining animals free of these disorders. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1274 / 1283
页数:10
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