Disruption of the beclin 1-BCL2 autophagy regulatory complex promotes longevity in mice

Nature. 2018 Jun;558(7708):136-140. doi: 10.1038/s41586-018-0162-7. Epub 2018 May 30.

Abstract

Autophagy increases the lifespan of model organisms; however, its role in promoting mammalian longevity is less well-established1,2. Here we report lifespan and healthspan extension in a mouse model with increased basal autophagy. To determine the effects of constitutively increased autophagy on mammalian health, we generated targeted mutant mice with a Phe121Ala mutation in beclin 1 (Becn1F121A/F121A) that decreases its interaction with the negative regulator BCL2. We demonstrate that the interaction between beclin 1 and BCL2 is disrupted in several tissues in Becn1 F121A/F121A knock-in mice in association with higher levels of basal autophagic flux. Compared to wild-type littermates, the lifespan of both male and female knock-in mice is significantly increased. The healthspan of the knock-in mice also improves, as phenotypes such as age-related renal and cardiac pathological changes and spontaneous tumorigenesis are diminished. Moreover, mice deficient in the anti-ageing protein klotho 3 have increased beclin 1 and BCL2 interaction and decreased autophagy. These phenotypes, along with premature lethality and infertility, are rescued by the beclin 1(F121A) mutation. Together, our data demonstrate that disruption of the beclin 1-BCL2 complex is an effective mechanism to increase autophagy, prevent premature ageing, improve healthspan and promote longevity in mammals.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / genetics
  • Aging / physiology*
  • Animals
  • Autophagosomes / metabolism
  • Autophagy / physiology*
  • Beclin-1 / genetics
  • Beclin-1 / metabolism*
  • Cells, Cultured
  • Female
  • Fibroblasts / cytology
  • Gene Knock-In Techniques
  • Glucuronidase / deficiency
  • Glucuronidase / genetics
  • HeLa Cells
  • Health
  • Humans
  • Klotho Proteins
  • Longevity / genetics
  • Longevity / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mutation
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*

Substances

  • Beclin-1
  • Proto-Oncogene Proteins c-bcl-2
  • Glucuronidase
  • Klotho Proteins