Abstract

MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression and have multiple effects in various tissues including adipose inflammation, a condition characterized by increased local release of the pro-lipolytic cytokine tumor necrosis factor-alpha (TNF-α). Whether miRNAs regulate adipocyte lipolysis is unknown. We set out to determine whether miRNAs affect adipocyte lipolysis in human fat cells. To this end, eleven miRNAs known to be present in human adipose tissue were over-expressed in human in vitro differentiated adipocytes followed by assessments of TNF-α and glycerol levels in conditioned media after 48 h. Three miRNAs (miR-145, -26a and let-7d) modulated both parameters in parallel. However, while miR-26a and let-7d decreased, miR-145 increased both glycerol release and TNF-α secretion. Further studies were focused therefore on miR-145 since this was the only stimulator of lipolysis and TNF-α secretion. Time-course analysis demonstrated that miR-145 over-expression up-regulated TNF-α expression/secretion followed by increased glycerol release. Increase in TNF-α production by miR-145 was mediated via activation of p65, a member of the NF-κB complex. In addition, miR-145 down-regulated the expression of the protease ADAM17, resulting in an increased fraction of membrane bound TNF-α, which is the more biologically active form of TNF-α. MiR-145 overexpression also increased the phosphorylation of activating serine residues in hormone sensitive lipase and decreased the mRNA expression of phosphodiesterase 3B, effects which are also observed upon TNF-α treatment in human adipocytes. We conclude that miR-145 regulates adipocyte lipolysis via multiple mechanisms involving increased production and processing of TNF-α in fat cells.

Highlights

  • Obesity and insulin resistance are characterized by several disturbances in white adipose tissue (WAT) function including increased basal lipolysis and a chronic low-grade inflammation

  • Screening of microRNAs Identifies tumour necrosis factor-alpha (TNF-a) as One Mediator of miRNA Effects on Human Adipocyte Lipolysis

  • In order to study whether microRNAs have an impact on adipocyte lipolysis, we selected a set of eleven miRNAs that we have previously described/identified as considerably and abundantly expressed in human WAT and isolated fat cells of a large number of subjects [18]

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Summary

Introduction

Obesity and insulin resistance are characterized by several disturbances in white adipose tissue (WAT) function including increased basal (i.e. non-hormone stimulated) lipolysis and a chronic low-grade inflammation. TNF-a affects lipolysis via multiple mechanisms mediated via its cognate receptor TNF-a-receptor-1 (TNFR1) [3] which in turn activate two main intracellular pathways: the mitogen activated protein kinases (MAPKs) (involving activation of ERK1/2 and JNK but not p38) [3,4,5] and NF-kB [6]. This results in increased phosphorylation and attenuated gene expression of perilipin-1 (PLIN1), a lipid droplet coating phosphoprotein that controls triglyceride hydrolysis by regulating access of hormone sensitive-lipase (HSL) to the lipid droplet surface [7]. TNF-a down-regulates phosphodiesterase 3B (PDE3B), the enzyme that catalyzes cAMP hydrolysis and which mediates the antilipolytic effect of insulin [9]

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