Crosstalk between bone marrow-derived mesenchymal stem cells and regulatory T cells through a glucocorticoid-induced leucine zipper/developmental endothelial locus-1-dependent mechanism

FASEB J. 2015 Sep;29(9):3954-63. doi: 10.1096/fj.15-273664. Epub 2015 Jun 2.

Abstract

Bone marrow is a reservoir for regulatory T (T(reg)) cells, but how T(reg) cells are regulated in that environment remains poorly understood. We show that expression of glucocorticoid (GC)-induced leucine zipper (GILZ) in bone marrow mesenchymal lineage cells or bone marrow-derived mesenchymal stem cells (BMSCs) increases the production of T(reg) cells via a mechanism involving the up-regulation of developmental endothelial locus-1 (Del-1), an endogenous leukocyte-endothelial adhesion inhibitor. We found that the expression of Del-1 is increased ∼4-fold in the bone tissues of GILZ transgenic (Tg) mice, and this increase is coupled with a significant increase in the production of IL-10 (2.80 vs. 0.83) and decrease in the production of IL-6 (0.80 vs. 2.33) and IL-12 (0.25 vs. 1.67). We also show that GILZ-expressing BMSCs present antigen in a way that favors T(reg) cells. These results indicate that GILZ plays a critical role mediating the crosstalk between BMSCs and T(reg) in the bone marrow microenvironment. These data, together with our previous findings that overexpression of GILZ in BMSCs antagonizes TNF-α-elicited inflammatory responses, suggest that GILZ plays important roles in bone-immune cell communication and BMSC immune suppressive functions.

Keywords: bone loss; bone marrow microenvironment; immune suppressive.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antigen Presentation / genetics
  • Antigen-Presenting Cells / cytology
  • Antigen-Presenting Cells / immunology*
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / immunology*
  • Calcium-Binding Proteins
  • Carrier Proteins / genetics
  • Carrier Proteins / immunology
  • Cell Adhesion Molecules
  • Cell Communication / genetics
  • Cell Communication / immunology*
  • Immune Tolerance / genetics
  • Intercellular Signaling Peptides and Proteins
  • Interleukin-10 / genetics
  • Interleukin-10 / immunology
  • Interleukin-6 / genetics
  • Interleukin-6 / immunology
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / immunology*
  • Mice
  • Mice, Transgenic
  • T-Lymphocytes, Regulatory / cytology
  • T-Lymphocytes, Regulatory / immunology*
  • Transcription Factors / genetics
  • Transcription Factors / immunology*
  • Tumor Necrosis Factor-alpha

Substances

  • Calcium-Binding Proteins
  • Carrier Proteins
  • Cell Adhesion Molecules
  • Dsip1 protein, mouse
  • Edil3 protein, mouse
  • IL10 protein, mouse
  • Intercellular Signaling Peptides and Proteins
  • Interleukin-6
  • Transcription Factors
  • Tumor Necrosis Factor-alpha
  • Interleukin-10