Fujihara Chiharu, Williams Joy A, Watanabe Masashi, Jeon Hyein, Sharrow Susan O, Hodes Richard J
Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892
J Immunol. 2014 Dec 1;193(11):5534-44. doi: 10.4049/jimmunol.1401655. Epub 2014 Oct 24.
Thymic development requires bidirectional interaction or cross-talk between developing T cells and thymic stromal cells, a relationship that has been best characterized for the interaction between thymocytes and thymic epithelial cells. We have characterized in this article the requirement for similar cross-talk in the maintenance and function of thymic B cells, another population that plays a role in selection of developing thymic T cells. We found that maintenance of thymic B cells is strongly dependent on the presence of mature single-positive thymocytes and on the interactions of these T cells with specific Ag ligand. Maintenance of thymic B cell number is strongly dependent on B cell-autonomous expression of CD40, but not MHC class II, indicating that direct engagement of CD40 on thymic B cells is necessary to support their maintenance and proliferation. Thymic B cells can mediate negative selection of superantigen-specific, self-reactive, single-positive thymocytes, and we show that CD40 expression on B cells is critical for this negative selection. Cross-talk with thymic T cells is thus required to support the thymic B cell population through a pathway that requires cell-autonomous expression of CD40, and that reciprocally functions in negative selection of autoreactive T cells.
胸腺发育需要发育中的T细胞与胸腺基质细胞之间进行双向相互作用或对话,这种关系在胸腺细胞与胸腺上皮细胞之间的相互作用中得到了最充分的表征。在本文中,我们描述了胸腺B细胞的维持和功能中类似对话的必要性,胸腺B细胞是另一个在发育中的胸腺T细胞选择中发挥作用的群体。我们发现,胸腺B细胞的维持强烈依赖于成熟单阳性胸腺细胞的存在以及这些T细胞与特定抗原配体的相互作用。胸腺B细胞数量的维持强烈依赖于CD40的B细胞自主表达,而不是MHC II类分子,这表明胸腺B细胞上CD40的直接结合对于支持其维持和增殖是必要的。胸腺B细胞可以介导超抗原特异性、自身反应性单阳性胸腺细胞的阴性选择,并且我们表明B细胞上的CD40表达对于这种阴性选择至关重要。因此,与胸腺T细胞的对话是通过一条需要CD40细胞自主表达的途径来支持胸腺B细胞群体的,并且在自身反应性T细胞的阴性选择中发挥相反的作用。