Department of Immunology, Weizmann Institute of Science, Herzel St 1, Rehovot 76100, Israel.
Department of Immunology, Weizmann Institute of Science, Herzel St 1, Rehovot 76100, Israel.
Immunity. 2015 Oct 20;43(4):776-87. doi: 10.1016/j.immuni.2015.08.015. Epub 2015 Sep 15.
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.
新兴证据表明,免疫机制是脂肪组织代谢控制的基础。在这里,我们展示了富含穿孔素颗粒的树突状细胞(perf-DC)这一罕见亚群的调节作用。通过骨髓移植生成选择性缺乏 perf-DC 的动物,我们发现这些嵌合体逐渐体重增加,并表现出代谢综合征的特征。这种表型与驻留在脂肪组织中的 T 细胞的 repertoire 改变有关,并且可以通过体内 T 细胞耗竭完全预防。在多发性硬化症的一种明确的实验自身免疫性脑脊髓炎(EAE)模型中也发现了 perf-DC 对炎症性 T 细胞的类似影响。因此,perf-DC 可能代表了一种关键的调节细胞亚群,对于预防代谢综合征和自身免疫至关重要。