The up-regulation of markers of adipose tissue fibrosis by visfatin in pre-adipocytes as well as obese children and adolescents

Cytokine. 2020 Oct:134:155193. doi: 10.1016/j.cyto.2020.155193. Epub 2020 Jul 21.

Abstract

Adipocytes are surrounded by a three-dimensional network of extracellular matrix (ECM) proteins. Aberrant ECM accumulation and remodeling leads to adipose tissue fibrosis. Visfatin is one of the adipocytokines that is increased in obesity and is implicated in insulin resistance. The objective of this study was to investigate the effect of visfatin on major components of ECM remodeling. In this study, plasma levels of both endotrophin and visfatin in obese children and adolescents were significantly higher than those in control subjects and they showed a positive correlation with each other. Treatment of 3T3-L1 pre-adipocytes with visfatin caused significant up-regulation of Osteopontin (Opn), Collagen type VI (Col6), matrix metalloproteinases MMP-2 and MMP-9. By using inhibitors of major signaling pathways it was shown that visfatin exerted its effect on Col6a3 gene expression through PI3K, JNK, and NF-кB pathways, while induced Opn gene expression via PI3K, JNK, MAPK/ERK, and NOTCH1. Our conclusion is that, the relationship between visfatin, endotrophin and insulin resistance parameters in obesity as well as increased expression of ECM proteins by visfatin suggests adipose tissue fibrosis as a mechanism for devastating effects of visfatin in obesity.

Keywords: Adipose tissue fibrosis; Collagen; Endotrophin; Insulin resistance; Metabolic syndrome; Obesity; Osteopontin; Visfatin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes*
  • Adipose Tissue / metabolism*
  • Adipose Tissue / pathology
  • Adolescent
  • Animals
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Case-Control Studies
  • Child
  • Collagen Type VI / blood
  • Collagen Type VI / genetics
  • Collagen Type VI / metabolism
  • Cytokines / blood
  • Cytokines / physiology*
  • Female
  • Fibrosis
  • Humans
  • Male
  • Matrix Metalloproteinases / biosynthesis
  • Matrix Metalloproteinases / genetics
  • Mice
  • Nicotinamide Phosphoribosyltransferase / blood
  • Nicotinamide Phosphoribosyltransferase / physiology*
  • Obesity / blood*
  • Osteopontin / genetics
  • Osteopontin / metabolism
  • Peptide Fragments / blood
  • Signal Transduction
  • Stem Cells / metabolism*
  • Up-Regulation

Substances

  • Biomarkers
  • COL6A3 protein, human
  • Collagen Type VI
  • Cytokines
  • Peptide Fragments
  • SPP1 protein, human
  • endotrophin
  • Osteopontin
  • Nicotinamide Phosphoribosyltransferase
  • nicotinamide phosphoribosyltransferase, human
  • Matrix Metalloproteinases