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Defects in mitophagy promote redox-driven metabolic syndrome in the absence of TP53INP1.

Marion Seillier | Laurent Pouyet | Prudence N'Guessan | Marie Nollet | Florence Capo | Fabienne Guillaumond | Laure Peyta | Jean-François Dumas | Annie Varrault | Gyslaine Bertrand | Stéphanie Bonnafous | Albert Tran | Gargi Meur | Piero Marchetti | Magalie A Ravier | Stéphane Dalle | Philippe Gual | Dany Muller | Guy A Rutter | Stéphane Servais | Juan L Iovanna | Alice Carrier
EMBO molecular medicine | 2015

The metabolic syndrome covers metabolic abnormalities including obesity and type 2 diabetes (T2D). T2D is characterized by insulin resistance resulting from both environmental and genetic factors. A genome-wide association study (GWAS) published in 2010 identified TP53INP1 as a new T2D susceptibility locus, but a pathological mechanism was not identified. In this work, we show that mice lacking TP53INP1 are prone to redox-driven obesity and insulin resistance. Furthermore, we demonstrate that the reactive oxygen species increase in TP53INP1-deficient cells results from accumulation of defective mitochondria associated with impaired PINK/PARKIN mitophagy. This chronic oxidative stress also favors accumulation of lipid droplets. Taken together, our data provide evidence that the GWAS-identified TP53INP1 gene prevents metabolic syndrome, through a mechanism involving prevention of oxidative stress by mitochondrial homeostasis regulation. In conclusion, this study highlights TP53INP1 as a molecular regulator of redox-driven metabolic syndrome and provides a new preclinical mouse model for metabolic syndrome clinical research.

Pubmed ID: 25828351

Research resources used in this publication

None found

Antibodies used in this publication

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Associated grants

  • Agency: Wellcome Trust, United Kingdom
    Id: 098424
  • Agency: Medical Research Council, United Kingdom
    Id: MR/K001981/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/J0003042/1
  • Agency: Wellcome Trust, United Kingdom
    Id: WT098424AIA

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