Fibroblast growth factor 21 improves insulin sensitivity and synergizes with insulin in human adipose stem cell-derived (hASC) adipocytes

PLoS One. 2014 Nov 3;9(11):e111767. doi: 10.1371/journal.pone.0111767. eCollection 2014.

Abstract

Fibroblast growth factor 21 (FGF21) has evolved as a major metabolic regulator, the pharmacological administration of which causes weight loss, insulin sensitivity and glucose control in rodents and humans. To understand the molecular mechanisms by which FGF21 exerts its metabolic effects, we developed a human in vitro model of adipocytes to examine crosstalk between FGF21 and insulin signaling. Human adipose stem cell-derived (hASC) adipocytes were acutely treated with FGF21 alone, insulin alone, or in combination. Insulin signaling under these conditions was assessed by measuring tyrosine phosphorylation of insulin receptor (InsR), insulin receptor substrate-1 (IRS-1), and serine 473 phosphorylation of Akt, followed by a functional assay using 14C-2-deoxyglucose [14C]-2DG to measure glucose uptake in these cells. FGF21 alone caused a modest increase of glucose uptake, but treatment with FGF21 in combination with insulin had a synergistic effect on glucose uptake in these cells. The presence of FGF21 also effectively lowered the insulin concentration required to achieve the same level of glucose uptake compared to the absence of FGF21 by 10-fold. This acute effect of FGF21 on insulin signaling was not due to IR, IGF-1R, or IRS-1 activation. Moreover, we observed a substantial increase in basal S473-Akt phosphorylation by FGF21 alone, in contrast to the minimal shift in basal glucose uptake. Taken together, our data demonstrate that acute co-treatment of hASC-adipocytes with FGF21 and insulin can result in a synergistic improvement in glucose uptake. These effects were shown to occur at or downstream of Akt, or separate from the canonical insulin signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism*
  • Adipose Tissue / metabolism*
  • Cells, Cultured
  • Drug Synergism
  • Fibroblast Growth Factors / agonists
  • Fibroblast Growth Factors / pharmacology*
  • Glucose / metabolism
  • Humans
  • Insulin / agonists
  • Insulin / pharmacology*
  • Insulin Receptor Substrate Proteins / metabolism
  • Insulin Resistance*
  • Receptor, Insulin / metabolism
  • Signal Transduction / drug effects
  • Stem Cells / metabolism*

Substances

  • IRS1 protein, human
  • Insulin
  • Insulin Receptor Substrate Proteins
  • fibroblast growth factor 21
  • Fibroblast Growth Factors
  • Receptor, Insulin
  • Glucose

Grants and funding

The study was paid for by Pfizer, CVMED. The funder provided support in the form of salaries for authors [D.V.L., D.L., Q.Y., Y.Z., B.G., R.C., M.B.B., S.T.], but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section.