AI Article Synopsis

  • Glucocorticoids are produced in adipose tissue and may promote metabolic diseases by aiding the expansion of fat tissue.
  • Exposure to glucocorticoids increases the sensitivity of human preadipocytes to insulin and enhances their differentiation response, while this effect is not seen in fully grown human fat cells or certain mouse cells.
  • The mechanism involves increased insulin signaling through various proteins, with initial influence from specific transcription factors, highlighting a new role for glucocorticoids in fat cell development.

Article Abstract

Glucocorticoids are synthesized locally in adipose tissue and contribute to metabolic disease through the facilitation of adipose tissue expansion. Here we report that exposure of human primary preadipocytes to glucocorticoids increases their sensitivity to insulin and enhances their subsequent response to stimuli that promote differentiation. This effect was observed in primary human preadipocytes but not in immortalized 3T3-L1 murine preadipocytes or in fully differentiated primary human adipocytes. Stimulation of insulin signaling was mediated through induction of insulin receptor (IR), IR substrate protein 1 (IRS1), IRS2, and the p85 regulatory subunit of phosphoinositide-3-3-kinase, which led to enhanced insulin-mediated activation of Akt. Although induction of IRS2 was direct, induction of IR and IRS1 by glucocorticoids occurred subsequent to primary induction of the forkhead family transcription factors FoxO1A and FoxO3A. These results reveal a new role for glucocorticoids in preparing preadipocytes for differentiation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428144PMC
http://dx.doi.org/10.1210/me.2009-0091DOI Listing

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