The AP-1 transcription factors c-Jun and JunB are essential for CD8α conventional dendritic cell identity

被引:24
作者
Novoszel, Philipp [1 ]
Drobits, Barbara [1 ]
Holcmann, Martin [1 ]
Fernandes, Cristiano De Sa [1 ]
Tschismarov, Roland [2 ]
Derdak, Sophia [3 ]
Decker, Thomas [2 ]
Wagner, Erwin F. [4 ,5 ]
Sibilia, Maria [1 ]
机构
[1] Med Univ Vienna, Inst Canc Res, Dept Med 1, Comprehens Canc Ctr, Vienna, Austria
[2] Univ Vienna, Dept Microbiol Immunobiol & Genet, Max Perutz Labs, Vienna, Austria
[3] Med Univ Vienna, Core Facil, Vienna, Austria
[4] Med Univ Vienna, Dept Dermatol, Vienna, Austria
[5] Med Univ Vienna, Dept Lab Med, Vienna, Austria
基金
奥地利科学基金会; 欧盟地平线“2020”; 欧洲研究理事会;
关键词
MICE LACKING JUNB; B-ATF; MOUSE; EXPRESSION; ID2; PROGENITORS; HOMEOSTASIS; SUBSETS; PROTEIN; IRF8;
D O I
10.1038/s41418-021-00765-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dendritic cell (DC) development is orchestrated by lineage-determining transcription factors (TFs). Although, members of the activator-protein-1 (AP-1) family, including Batf3, have been implicated in conventional (c)DC specification, the role of Jun proteins is poorly understood. Here, we identified c-Jun and JunB as essential for cDC1 fate specification and function. In mice, Jun proteins regulate extrinsic and intrinsic pathways, which control CD8 alpha cDC1 diversification, whereas CD103 cDC1 development is unaffected. The loss of c-Jun and JunB in DC progenitors diminishes the CD8 alpha cDC1 pool and thus confers resistance to Listeria monocytogenes infection. Their absence in CD8 alpha cDC1 results in impaired TLR triggering and antigen cross-presentation. Both TFs are required for the maintenance of the CD8 alpha cDC1 subset and suppression of cDC2 identity on a transcriptional and phenotypic level. Taken together, these results demonstrate the essential role of c-Jun and JunB in CD8 alpha cDC1 diversification, function, and maintenance of their identity.
引用
收藏
页码:2404 / 2420
页数:17
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