Maternal Metabolic Syndrome Programs Mitochondrial Dysfunction via Germline Changes across Three Generations

Jessica L. Saben(Washington University in St. Louis), Anna L. Boudoures(Washington University in St. Louis), Zeenat A. Shyr(Washington University in St. Louis), Alysha Thompson(Washington University in St. Louis), Andrea Drury(Washington University in St. Louis), Wendy Zhang(Washington University in St. Louis), Maggie Chi(Washington University in St. Louis), Andrew Cusumano(Washington University in St. Louis), Suzanne M. Scheaffer(Washington University in St. Louis), Kelle H. Moley(Washington University in St. Louis)
Cell Reports
June 1, 2016
Cited by 267Open Access
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Abstract

Maternal obesity impairs offspring health, but the responsible mechanisms are not fully established. To address this question, we fed female mice a high-fat/high-sugar diet from before conception until weaning and then followed the outcomes in the next three generations of offspring, all fed a control diet. We observed that female offspring born to obese mothers had impaired peripheral insulin signaling that was associated with mitochondrial dysfunction and altered mitochondrial dynamic and complex proteins in skeletal muscle. This mitochondrial phenotype persisted through the female germline and was passed down to the second and third generations. Our results indicate that maternal programming of metabolic disease can be passed through the female germline and that the transfer of aberrant oocyte mitochondria to subsequent generations may contribute to the increased risk for developing insulin resistance.


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