Mast cell-deficient Kit(W-sh) "Sash" mutant mice display aberrant myelopoiesis leading to the accumulation of splenocytes that act as myeloid-derived suppressor cells

J Immunol. 2013 Jun 1;190(11):5534-44. doi: 10.4049/jimmunol.1203355. Epub 2013 May 1.

Abstract

Mast cell-deficient Kit(W-sh) "sash" mice are widely used to investigate mast cell functions. However, mutations of c-Kit also affect additional cells of hematopoietic and nonimmune origin. In this study, we demonstrate that Kit(W-sh) causes aberrant extramedullary myelopoiesis characterized by the expansion of immature lineage-negative cells, common myeloid progenitors, and granulocyte/macrophage progenitors in the spleen. A consistent feature shared by these cell types is the reduced expression of c-Kit. Populations expressing intermediate and high levels of Ly6G, a component of the myeloid differentiation Ag Gr-1, are also highly expanded in the spleen of sash mice. These cells are able to suppress T cell responses in vitro and phenotypically and functionally resemble myeloid-derived suppressor cells (MDSC). MDSC typically accumulate in tumor-bearing hosts and are able to dampen immune responses. Consequently, transfer of MDSC from naive sash mice into line 1 alveolar cell carcinoma tumor-bearing wild-type littermates leads to enhanced tumor progression. However, although it can also be observed in sash mice, accelerated growth of transplanted line 1 alveolar cell carcinoma tumors is a mast cell-independent phenomenon. Thus, the Kit(W-sh) mutation broadly affects key steps in myelopoiesis that may have an impact on mast cell research.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adoptive Transfer
  • Animals
  • Antigens, Ly / metabolism
  • CD11b Antigen / metabolism
  • Female
  • Hematopoiesis, Extramedullary / genetics
  • Hematopoiesis, Extramedullary / immunology
  • Immunophenotyping
  • Mast Cells / immunology*
  • Mast Cells / metabolism
  • Mice
  • Mice, Knockout
  • Mutation*
  • Myeloid Cells / immunology*
  • Myeloid Cells / metabolism
  • Myelopoiesis / genetics*
  • Myelopoiesis / immunology*
  • Neoplasm Transplantation
  • Neoplasms / immunology
  • Neoplasms / pathology
  • Proto-Oncogene Proteins c-kit / deficiency
  • Proto-Oncogene Proteins c-kit / genetics*
  • Spleen / cytology*
  • Spleen / immunology
  • Spleen / metabolism

Substances

  • Antigens, Ly
  • CD11b Antigen
  • Ly-6C antigen, mouse
  • Ly6G antigen, mouse
  • Proto-Oncogene Proteins c-kit