上皮内淋巴细胞
CD8型
生物
细胞毒性T细胞
免疫学
BCL6公司
胸腺细胞
T细胞受体
淋巴细胞生成
分子生物学
细胞生物学
T细胞
抗原
遗传学
免疫系统
造血
B细胞
干细胞
抗体
体外
生发中心
作者
Qi Xing,Dehui Chang,Shiyuan Xie,Xiaohong Zhao,Hao Zhang,Xiaohu Wang,Xue Bai,Chen Dong
出处
期刊:Science immunology
[American Association for the Advancement of Science (AAAS)]
日期:2024-02-09
卷期号:9 (92)
被引量:3
标识
DOI:10.1126/sciimmunol.adk4348
摘要
TCRαβ + CD8αα + intraepithelial lymphocytes (CD8αα + αβ IELs) are a specialized subset of T cells in the gut epithelium that develop from thymic agonist selected IEL precursors (IELps). The molecular mechanisms underlying the selection and differentiation of this T cell type in the thymus are largely unknown. Here, we found that Bcl6 deficiency in αβ T cells resulted in the near absence of CD8αα + αβ IELs. BCL6 was expressed by approximately 50% of CD8αα + αβ IELs and by the majority of thymic PD1 + IELps after agonist selection. Bcl6 deficiency blocked early IELp generation in the thymus, and its expression in IELps was induced by thymic TCR signaling in an ERK-dependent manner. As a result of Bcl6 deficiency, the precursors of IELps among CD4 + CD8 + double-positive thymocytes exhibited increased apoptosis during agonist selection and impaired IELp differentiation and maturation. Together, our results elucidate BCL6 as a crucial transcription factor during the thymic development of CD8αα + αβ IELs.
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