Programming of adipose tissue miR-483-3p and GDF-3 expression by maternal diet in type 2 diabetes

Cell Death Differ. 2012 Jun;19(6):1003-12. doi: 10.1038/cdd.2011.183. Epub 2012 Jan 6.

Abstract

Nutrition during early mammalian development permanently influences health of the adult, including increasing the risk of type 2 diabetes and coronary heart disease. However, the molecular mechanisms underlying such programming are poorly defined. Here we demonstrate that programmed changes in miRNA expression link early-life nutrition to long-term health. Specifically, we show that miR-483-3p is upregulated in adipose tissue from low-birth-weight adult humans and prediabetic adult rats exposed to suboptimal nutrition in early life. We demonstrate that manipulation of miR-483-3p levels in vitro substantially modulates the capacity of adipocytes to differentiate and store lipids. We show that some of these effects are mediated by translational repression of growth/differentiation factor-3, a target of miR-483-3p. We propose that increased miR-483-3p expression in vivo, programmed by early-life nutrition, limits storage of lipids in adipose tissue, causing lipotoxicity and insulin resistance and thus increasing susceptibility to metabolic disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions
  • Adipose Tissue / metabolism*
  • Adult
  • Animals
  • Animals, Newborn
  • Base Sequence
  • Cell Differentiation
  • Diabetes Mellitus, Type 2 / metabolism*
  • Diabetes Mellitus, Type 2 / pathology
  • Diet*
  • Disease Models, Animal
  • Down-Regulation
  • Female
  • Growth Differentiation Factor 3 / antagonists & inhibitors
  • Growth Differentiation Factor 3 / genetics
  • Growth Differentiation Factor 3 / metabolism*
  • HEK293 Cells
  • Humans
  • Lipid Metabolism
  • Male
  • MicroRNAs / metabolism*
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Rats
  • Rats, Wistar

Substances

  • 3' Untranslated Regions
  • Growth Differentiation Factor 3
  • MicroRNAs
  • RNA, Small Interfering