Insulin regulates leptin secretion from 3T3-L1 adipocytes by a PI 3 kinase independent mechanism. Academic Article uri icon

Overview

abstract

  • To better define the molecular mechanisms underlying leptin release from adipocytes, we developed a novel protocol that maximizes leptin production from 3T3-L1 adipocytes. The addition of a PPARgamma agonist to the Isobutylmethylxanthine/Dexamethasone/Insulin differentiation cocktail increased leptin mRNA levels by 5-fold, maintained insulin sensitivity, and yielded mature phenotype in cultured adipocytes. Under these conditions, acute insulin stimulation for 2 h induced a two-fold increase in leptin secretion, which was independent of new protein synthesis, and was not due to alterations in glucose metabolism. Stimulation with insulin for 15 min induced the same level of leptin release and was blocked by Brefeldin A. Inhibiting PI 3-kinase with wortmannin had no effect on insulin stimulation of leptin secretion. These studies show that insulin can stimulate leptin release via a PI3K independent mechanism and provide a cellular system for studying the effect of insulin and potentially other mediators on leptin secretion.

publication date

  • April 12, 2008

Research

keywords

  • 3T3-L1 Cells
  • Adipocytes
  • Insulin
  • Leptin
  • Phosphatidylinositol 3-Kinases
  • Signal Transduction

Identity

PubMed Central ID

  • PMC2997521

Scopus Document Identifier

  • 45049085823

Digital Object Identifier (DOI)

  • 10.1016/j.yexcr.2008.04.003

PubMed ID

  • 18501893

Additional Document Info

volume

  • 314

issue

  • 11-12