Macrophage-conditioned medium inhibits the differentiation of 3T3-L1 and human abdominal preadipocytes

Diabetologia. 2006 Jun;49(6):1402-11. doi: 10.1007/s00125-006-0253-0. Epub 2006 Apr 12.

Abstract

Aims/hypothesis: In obesity, a limited adipogenic capacity may promote adipocyte hypertrophy and increase the risk of insulin resistance and type 2 diabetes. Recent data indicate that macrophages reside within adipose tissue in obese rodents and humans. We hypothesised that secreted macrophage factors may inhibit adipogenesis.

Materials and methods: Conditioned media from cultured murine J774 or human THP-1 macrophages were collected, and added to either murine 3T3-L1 preadipocytes or human abdominal stromal preadipocytes from subcutaneous or omental fat depots.

Results: Macrophage-conditioned medium (MacCM) strongly inhibited 3T3-L1 adipogenesis. Dose-response studies with J774-MacCM revealed that 80 and 100% of J774-MacCM completely suppressed triacylglycerol accumulation as well as the induction of fatty acid synthase, peroxisome proliferator-activated receptor gamma, CCAAT/enhancer binding protein alpha, and adiponectin. Similar inhibitory effects on 3T3-L1 preadipocytes were observed with THP-1-MacCM. Differentiation of human abdominal subcutaneous stromal preadipocytes was moderately reduced (subcutaneous>omental) by J744-MacCM. In contrast, the differentiation of both subcutaneous and omental stromal preadipocytes was completely inhibited by THP-1-MacCM, as determined on the basis of morphology and triacylglycerol accumulation, as well as fatty acid synthase and adiponectin protein expression.

Conclusions/interpretation: Secreted macrophage products inhibit the differentiation of 3T3-L1 preadipocytes as well as human abdominal stromal preadipocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells / cytology*
  • Abdomen
  • Adipocytes / cytology*
  • Animals
  • Cell Culture Techniques
  • Cell Differentiation / physiology*
  • Cell Survival
  • Culture Media, Conditioned
  • Humans
  • Macrophages / physiology*
  • Mice
  • Monocytes / cytology

Substances

  • Culture Media, Conditioned