Microparticles release by adipocytes act as "find-me" signals to promote macrophage migration

Akiko Eguchi1, Anny Mulya2, Milos Lazic1

  • 1Department of Pediatrics, University of California San Diego (UCSD), La Jolla, California, United States of America.

Plos One
|April 8, 2015
PubMed

Insights

Adipocyte-derived microparticles (MPs) act as critical signals attracting macrophages to adipose tissue during obesity. This discovery sheds light on obesity

Area of Science:

  • Immunology
  • Metabolic Disease Research
  • Cell Biology

Background:

  • Macrophage infiltration into adipose tissue is a key factor in obesity-related metabolic dysfunction.
  • The precise mechanisms recruiting macrophages to obese adipose tissue are not fully understood.

Purpose of the Study:

  • To investigate the role of adipocyte-derived microparticles (MPs) as signals attracting monocytes and macrophages to adipose tissue.
  • To elucidate the regulatory pathways involved in the release and function of these MPs.

Main Methods:

  • Stimulation of adipocytes with saturated fatty acids and observation of supernatant effects on immune cells.
  • Analysis of caspase 3 activation and Rho-associated kinase involvement in MP release.
  • In vitro and in vivo assessment of MP chemoattractant properties.
  • Transplantation of circulating MPs from obese mice into wild-type mice.

Main Results:

  • Stressed adipocytes release microparticles (MPs) that attract monocytes and macrophages.
  • Caspase 3 activation is essential for the release of these chemoattractant MPs.
  • Obesity models exhibit elevated levels of circulating adipocyte-derived MPs.
  • Adipocyte-derived MPs function as potent chemoattractants both in vitro and in vivo.
  • Transplanted MPs from obese mice induced monocyte activation in recipient mice.

Conclusions:

  • Adipocyte-derived MPs serve as crucial "find-me" signals mediating macrophage recruitment in obesity.
  • Targeting these MPs may offer a novel therapeutic strategy for obesity-associated metabolic complications.