Center for Biotechnology and Genomic Medicine, Medical College of Georgia, Augusta, GA 30912, USA.
J Immunol. 2011 Jul 1;187(1):248-57. doi: 10.4049/jimmunol.1003785. Epub 2011 Jun 3.
Despite their importance for the functioning of the immune system, thymic development and peripheral maintenance of Foxp3(+) regulatory T (T(R)) cells are poorly understood. We have found that connexin 43 (Cx43), expressed by thymic T(R) cells progenitors, supports T(R) development. Mice with deletion of the Cx43 gene induced in T cells produce only few T(R) cells and had increased proportion of activated T cells in the lymph nodes, suggesting impaired peripheral tolerance. Reduction of the T(R) cell numbers was accompanied by increased presence of CD4(+)CD25(+)GITR(+)Foxp3(-) T cells, which did not produce inflammatory cytokines and lost suppressor function. These results strongly argue that we have discovered a novel signaling pathway, controlled by Cx43, that enhances the generation of T(R) cells. We propose that a possible mechanism of Cx43 activity is by regulating Foxp3 expression in T(R) lineage cells.
尽管它们对免疫系统的功能至关重要,但胸腺发育和外周维持 Foxp3(+)调节性 T (T(R))细胞的机制仍知之甚少。我们发现,表达于胸腺 T(R)细胞前体的连接蛋白 43 (Cx43)支持 T(R)细胞的发育。在 T 细胞中诱导缺失 Cx43 基因的小鼠仅产生少量的 T(R)细胞,并且淋巴结中活化 T 细胞的比例增加,提示外周耐受受损。T(R)细胞数量的减少伴随着 CD4(+)CD25(+)GITR(+)Foxp3(-)T 细胞的增加,这些细胞不产生炎症细胞因子且丧失了抑制功能。这些结果强烈表明,我们已经发现了一种由 Cx43 控制的新型信号通路,可增强 T(R)细胞的生成。我们提出,Cx43 活性的可能机制是通过调节 T(R)细胞谱系细胞中的 Foxp3 表达。