Secreted αKlotho isoform protects against age-dependent memory deficits

被引:35
|
作者
Masso, A. [1 ,2 ]
Sanchez, A. [1 ,2 ]
Bosch, A. [1 ,2 ,3 ]
Gimenez-Llort, L. [2 ,4 ]
Chillon, M. [1 ,2 ,5 ,6 ]
机构
[1] Univ Autonoma Barcelona, Dept Biochem & Mol Biol, Inst Neurociencies, 5th Level,Edifici H,Campus UAB, Bellaterra 08193, Spain
[2] Univ Autonoma Barcelona, Inst Neurociences INc, Campus UAB, Bellaterra, Spain
[3] Inst Carlos III, Ctr Invest Biomed Red Enfermedades Neurodegenerat, Madrid, Spain
[4] Univ Autonoma Barcelona, Sch Med, Dept Psychiat & Forens Med, Campus UAB, Bellaterra, Spain
[5] VHIR, Res Grp Gene Therapy Nervous Syst, Barcelona, Spain
[6] ICREA, Barcelona, Spain
关键词
ALZHEIMERS-DISEASE; ANOREXIA-NERVOSA; GENE; MOUSE; MICE; ACETYL-1-CARNITINE; PERFORMANCE; EXPRESSION; MORTALITY; SYMPTOMS;
D O I
10.1038/mp.2017.211
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
alpha Klotho is a gene regulator of aging, increasing life expectancy when overexpressed and accelerating the development of aging phenotypes when inhibited. In mice, expression levels of the secreted isoform Klotho (s-KL) are very high in the brain, suggesting that s-KL activity may have an important role in the nervous system. Here we study the functional relevance at behavioural level of modifying s-KL levels in the aging brain. We used AAVrh10 vectors to deliver and sustained expression of s-KL in 6- and 12-month-old wild-type C57BL/6J males. This study demonstrates for we believe the first time in vivo that 6 months after a single injection of s-KL into the central nervous system, long-lasting and quantifiable enhancement of learning and memory capabilities are found. More importantly, cognitive improvement is also observable in 18-month-old mice treated once, at 12 months of age. These findings demonstrate the therapeutic potential of s-KL as a treatment for cognitive decline associated with aging.
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页码:1937 / 1947
页数:11
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