生物
谱系(遗传)
先天性淋巴细胞
树突状细胞
免疫系统
转录因子
细胞生物学
祖细胞
免疫学
先天免疫系统
祖细胞
细胞分化
抗原
滤泡树突状细胞
免疫耐受
T细胞
获得性免疫系统
免疫
利基
骨髓
FOXP3型
抗原提呈细胞
基因
调节性T细胞
粘膜免疫学
干细胞
周边公差
细胞
作者
Patrick Fernandes Rodrigues,Shitong Wu,Tihana Trsan,Bishan Bhattarai,Santosh K. Panda,José Luís Fachi,Marina Cella,Marco Colonna
出处
期刊:Science immunology
[American Association for the Advancement of Science (AAAS)]
日期:2026-01-27
卷期号:: eaed7439-eaed7439
标识
DOI:10.1126/sciimmunol.aed7439
摘要
How tolerogenic dendritic cell (DC) lineages are established to prevent inappropriate immune responses to commensals and food antigens remains unclear. We identify RORγt + DCs in mice as a distinct lymphoid-derived lineage to safeguard intestinal tolerance. Using lineage tracing and single-cell transcriptomics, we unveiled bone marrow–resident Rorc(t) + progenitors, which include a RORγt + innate lymphoid progenitor (RILP) that generates both ILC3s and RORγt + DCs, and a pre-RORγt + DC precursor committed exclusively to the RORγt + DC lineage. RORγt + DC development required the Rorc +7 kb enhancer, whose accessibility was ensured by the repressors REV-ERBα and REV-ERBβ, and depended on the transcription factors PRDM16 and PU.1 for lineage commitment. Loss of any of these regulators abrogated RORγt + DC differentiation, reduced peripheral regulatory T (T reg ) cell induction, and skewed toward T helper 2 responses. Together, these findings define murine RORγt + DCs as a lymphoid-derived lineage whose enhancer- and transcription factor–driven development is essential for peripheral T reg cell-mediated immune homeostasis.
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