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Involvement of miR-3180-3p and miR-4632-5p in palmitic acid-induced insulin resistance.

Abstract
Insulin resistance is defined as a failure to trigger the activation of the PI3K-AKT pathway by normal levels of insulin; therefore, it is well linked to metabolic disorders. Although multiple mechanisms contribute to insulin resistance, one major cause is elevated concentrations of plasma free fatty acids, which are known to suppress insulin signaling. However, the underlying mechanism is still elusive. Here, we found that palmitic acid increased the expression of two miRNAs, miR-3180-3p and miR-4632-5p, in HepG2 cells. Transfection of HepG2 cells with miR-3180-3p or miR-4632-5p reduced insulin-induced activation of the PI3K-AKT pathway. Moreover, palmitic acid or two miRNAs inhibited insulin-induced phosphorylation of Tyr612 on IRS-1 without affecting insulin receptor activation. Therefore, two miRNAs are suggested to be involved in palmitic acid-induced insulin resistance through suppression of insulin-induced IRS-1 phosphorylation. Identification of miR-3180-3p and miR-4632-5p targets could provide valuable information for the development of therapeutic drugs for type 2 diabetes.
AuthorsEtsu Tashiro, Yumi Nagasawa, Susumu Itoh, Masaya Imoto
JournalMolecular and cellular endocrinology (Mol Cell Endocrinol) Vol. 534 Pg. 111371 (08 20 2021) ISSN: 1872-8057 [Electronic] Ireland
PMID34157350 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2021 Elsevier B.V. All rights reserved.
Chemical References
  • IRS1 protein, human
  • Insulin
  • Insulin Receptor Substrate Proteins
  • MicroRNAs
  • Palmitic Acid
  • Proto-Oncogene Proteins c-akt
Topics
  • Gene Expression Regulation (drug effects)
  • Hep G2 Cells
  • Humans
  • Insulin (metabolism)
  • Insulin Receptor Substrate Proteins (metabolism)
  • Insulin Resistance (genetics)
  • MicroRNAs (genetics)
  • Models, Biological
  • Palmitic Acid (adverse effects)
  • Phosphatidylinositol 3-Kinases (metabolism)
  • Phosphorylation
  • Proto-Oncogene Proteins c-akt (metabolism)
  • Signal Transduction
  • Up-Regulation

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