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PLoS One ; 12(4): e0176371, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28448551

RESUMO

The NAD+-dependent SIRT6 deacetylase was shown to be a major regulator of lifespan and healthspan. Mice deficient for SIRT6 develop a premature aging phenotype and metabolic defects, and die before four weeks of age. Thus, the effect of SIRT6 deficiency in adult mice is unknown. Here we show that SIRT6-/- mice in mixed 129/SvJ/BALB/c background reach adulthood, allowing examination of SIRT6-related metabolic and developmental phenotypes in adult mice. In this mixed background, at 200 days of age, more than 80% of the female knock-out mice were alive whereas only 10% of male knock-out mice survived. In comparison to their wild-type littermates, SIRT6 deficient mice have reduced body weight, increased glucose uptake and exhibit an age-dependent progressive impairment of retinal function accompanied by thinning of retinal layers. Together, these results demonstrate a role for SIRT6 in metabolism and age-related ocular changes in adult mice and suggest a gender specific regulation of lifespan by SIRT6.


Assuntos
Técnicas de Inativação de Genes , Sirtuínas/deficiência , Sirtuínas/genética , Adiposidade/genética , Envelhecimento/genética , Envelhecimento/metabolismo , Animais , Transporte Biológico/genética , Peso Corporal/genética , Feminino , Glucose/metabolismo , Masculino , Camundongos , Fenótipo
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