Insulin regulates leptin secretion from 3T3–L1 adipocytes by a PI 3 kinase independent mechanism

A Zeigerer, MS Rodeheffer, TE McGraw… - Experimental cell …, 2008 - Elsevier
A Zeigerer, MS Rodeheffer, TE McGraw, JM Friedman
Experimental cell research, 2008Elsevier
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 PPARγ 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 …
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 PPARγ 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.
Elsevier