| Literature DB >> 26384546 |
Yael Zlotnikov-Klionsky1, Bar Nathansohn-Levi1, Elias Shezen1, Chava Rosen1, Sivan Kagan1, Liat Bar-On1, Steffen Jung1, Eric Shifrut1, Shlomit Reich-Zeliger1, Nir Friedman1, Rina Aharoni1, Ruth Arnon1, Oren Yifa1, Anna Aronovich1, Yair Reisner2.
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.Entities:
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Year: 2015 PMID: 26384546 DOI: 10.1016/j.immuni.2015.08.015
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745