Perforin-Positive Dendritic Cells Exhibit an Immuno-regulatory Role in Metabolic Syndrome and Autoimmunity

Immunity. 2015 Oct 20;43(4):776-87. doi: 10.1016/j.immuni.2015.08.015. Epub 2015 Sep 15.

Abstract

Emerging evidence suggests that immunological mechanisms underlie metabolic control of adipose tissue. Here, we have shown the regulatory impact of a rare subpopulation of dendritic cells, rich in perforin-containing granules (perf-DCs). Using bone marrow transplantation to generate animals selectively lacking perf-DCs, we found that these chimeras progressively gained weight and exhibited features of metabolic syndrome. This phenotype was associated with an altered repertoire of T cells residing in adipose tissue and could be completely prevented by T cell depletion in vivo. A similar impact of perf-DCs on inflammatory T cells was also found in a well-defined model of multiple sclerosis, experimental autoimmune encephlalomyelitis (EAE). Thus, perf-DCs probably represent a regulatory cell subpopulation critical for protection from metabolic syndrome and autoimmunity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / immunology
  • Adipose Tissue / metabolism
  • Adipose Tissue / pathology
  • Adoptive Transfer
  • Animals
  • Antigens, Differentiation / analysis
  • Autoimmunity / immunology*
  • CD11c Antigen / analysis
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / pathology
  • CD8-Positive T-Lymphocytes / transplantation
  • Clone Cells / immunology
  • Cytoplasmic Granules / chemistry
  • Dendritic Cells / classification
  • Dendritic Cells / immunology*
  • Dendritic Cells / ultrastructure
  • Diet, High-Fat / adverse effects
  • Encephalomyelitis, Autoimmune, Experimental / immunology
  • Encephalomyelitis, Autoimmune, Experimental / pathology
  • Female
  • Inflammation / immunology*
  • Inflammation / pathology
  • Lymphocyte Depletion
  • Male
  • Metabolic Syndrome / etiology
  • Metabolic Syndrome / immunology*
  • Metabolic Syndrome / pathology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Obesity / immunology
  • Obesity / pathology
  • Phenotype
  • Pore Forming Cytotoxic Proteins / analysis*
  • Pore Forming Cytotoxic Proteins / deficiency
  • Pore Forming Cytotoxic Proteins / genetics
  • Radiation Chimera
  • Self Tolerance / immunology

Substances

  • Antigens, Differentiation
  • CD11c Antigen
  • Pore Forming Cytotoxic Proteins
  • perforin, mouse