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MicroRNA-16 modulates macrophage polarization leading to improved insulin sensitivity in myoblasts.

Abstract
Uncontrolled inflammation leads to several diseases such as insulin resistance, T2D and several types of cancers. The functional role of microRNAs in inflammation induced insulin resistance is poorly studied. MicroRNAs are post-transcriptional regulatory molecules which mediate diverse biological processes. We here show that miR-16 expression levels are down-regulated in different inflammatory conditions such as LPS/IFNγ or palmitate treated macrophages, palmitate exposed myoblasts and insulin responsive tissues of high sucrose diet induced insulin resistant rats. Importantly, forced expression of miR-16 in macrophages impaired the production of TNF-α, IL-6 and IFN-β leading to enhanced insulin stimulated glucose uptake in co-cultured skeletal myoblasts. Further, ectopic expression of miR-16 enhanced insulin stimulated glucose uptake in skeletal myoblasts via the up-regulation of GLUT4 and MEF2A, two key players involved in insulin stimulated glucose uptake. Collectively, our data highlight the important role of miR-16 in ameliorating inflammation induced insulin resistance.
AuthorsMalathi Talari, Bandish Kapadia, Vasundhara Kain, Sriram Seshadri, Bhumika Prajapati, Parth Rajput, Parimal Misra, Kishore V L Parsa
JournalBiochimie (Biochimie) Vol. 119 Pg. 16-26 (Dec 2015) ISSN: 1638-6183 [Electronic] France
PMID26453808 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2015 Elsevier B.V. and Société Française de Biochimie et Biologie Moléculaire (SFBBM). All rights reserved.
Chemical References
  • Dietary Sucrose
  • Endotoxins
  • Fatty Acids, Nonesterified
  • MIRN16 microRNA, rat
  • MicroRNAs
  • Mirn16 microRNA, mouse
  • Recombinant Proteins
  • endotoxin, Escherichia coli
  • Interferon-gamma
Topics
  • Animals
  • Cell Communication (drug effects)
  • Cell Line
  • Cell Polarity (drug effects)
  • Coculture Techniques
  • Dietary Sucrose (adverse effects)
  • Down-Regulation (drug effects)
  • Endotoxins (toxicity)
  • Fatty Acids, Nonesterified (adverse effects)
  • Insulin Resistance
  • Interferon-gamma (genetics, metabolism, pharmacology)
  • Macrophage Activation (drug effects)
  • Macrophages (drug effects, immunology, metabolism)
  • Mice
  • MicroRNAs (antagonists & inhibitors, metabolism)
  • Muscle, Skeletal (metabolism)
  • Myoblasts (drug effects, immunology, metabolism)
  • RAW 264.7 Cells
  • Rats
  • Rats, Wistar
  • Recombinant Proteins (metabolism, pharmacology)

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