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Cell Death Differ ; 19(6): 1003-12, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22223106

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.


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