STAT of the union: dynamics of distinct tumor-associated macrophage subsets governed by STAT1

Eur J Immunol. 2014 Aug;44(8):2238-42. doi: 10.1002/eji.201444870.

Abstract

The tumor stroma has long been ignored as therapeutic target, but it has become clear that several stromal cell types play a nonredundant role during tumor progression. In particular, macrophages possess the capacity to stimulate tumor growth and metastasis via multiple mechanisms. In this issue of the European Journal of Immunology, a study by Tymoszuk et al. Eur. J. Immunol. 2014. 44: 2247-2262 demonstrates that both monocyte recruitment and local macrophage proliferation determines the tumor-associated macrophage (TAM) pool size in HER2/Neu-driven mammary carcinomas. These tumors contain two main TAM subsets--MHC class II (MHC-II)(lo) F4/80(hi) and MHC-II(hi) F4/80(lo)--similar to what was observed in other tumor models. Interestingly, only the MHC-II(lo) F4/80(hi) subset is largely absent in a STAT1-deficient background. STAT1 induces the expression of CSF-1, which in turn drives TAM proliferation and possibly also the M2 gene signature of MHC-II(lo) F4/80(hi) TAM. Conversely, STAT1 deficiency upregulates M2 gene expression in MHC-II(hi) F4/80(lo) TAM, demonstrating that both TAM subsets are differentially regulated, probably as a consequence of their distinct intratumoral localization. In this Commentary, we place these findings in the context of current knowledge and propose new avenues for future research.

Keywords: CSF-1; Ontogeny; Stat1; Tumor-associated macrophages.

MeSH terms

  • Breast Neoplasms / immunology
  • Breast Neoplasms / metabolism
  • Cell Proliferation
  • Female
  • Genes, MHC Class II / immunology
  • Humans
  • Macrophage Colony-Stimulating Factor / immunology
  • Macrophage Colony-Stimulating Factor / metabolism
  • Macrophages / immunology*
  • Macrophages / metabolism*
  • Monocytes / immunology
  • Monocytes / metabolism
  • Receptor, ErbB-2 / metabolism
  • STAT1 Transcription Factor / immunology
  • STAT1 Transcription Factor / metabolism*

Substances

  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Macrophage Colony-Stimulating Factor
  • Receptor, ErbB-2