Mucosal Immunology Unit, Oral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland, USA.
Nat Immunol. 2011 Apr;12(4):312-9. doi: 10.1038/ni.1997. Epub 2011 Feb 6.
The molecular mechanisms that direct the development of TCRαβ+CD8αα+ intestinal intraepithelial lymphocytes (IELs) are not thoroughly understood. Here we show that transforming growth factor-β (TGF-β) controls the development of TCRαβ+CD8αα+ IELs. Mice with either a null mutation in the gene encoding TGF-β1 or T cell-specific deletion of TGF-β receptor I lacked TCRαβ+CD8αα+ IELs, whereas mice with transgenic overexpression of TGF-β1 had a larger population of TCRαβ+CD8αα+ IELs. We observed defective development of the TCRαβ+CD8αα+ IEL thymic precursors (CD4⁻CD8⁻TCRαβ+CD5+) in the absence of TGF-β. In addition, we found that TGF-β signaling induced CD8α expression in TCRαβ+CD8αα+ IEL thymic precursors and induced and maintained CD8α expression in peripheral populations of T cells. Our data demonstrate a previously unrecognized role for TGF-β in the development of TCRαβ+CD8αα+ IELs and the expression of CD8α in T cells.
T 细胞受体 αβ+CD8αα+肠道上皮内淋巴细胞(IEL)发育的分子机制尚不完全清楚。在这里,我们表明转化生长因子-β(TGF-β)控制着 TCRαβ+CD8αα+IEL 的发育。TGF-β1 编码基因缺失或 T 细胞特异性 TGF-β 受体 I 缺失的小鼠缺乏 TCRαβ+CD8αα+IEL,而 TGF-β1 转基因过表达的小鼠则具有更大数量的 TCRαβ+CD8αα+IEL。我们观察到在没有 TGF-β 的情况下,TCRαβ+CD8αα+IEL 胸腺前体(CD4⁻CD8⁻TCRαβ+CD5+)的发育缺陷。此外,我们发现 TGF-β 信号诱导 TCRαβ+CD8αα+IEL 胸腺前体中 CD8α 的表达,并诱导和维持外周 T 细胞群体中 CD8α 的表达。我们的数据表明 TGF-β 在 TCRαβ+CD8αα+IEL 的发育和 T 细胞中 CD8α 的表达中具有先前未被认识的作用。