| Literature DB >> 30611612 |
Michaël Chopin1, Aaron T Lun2, Yifan Zhan2, Jaring Schreuder2, Hannah Coughlan2, Angela D'Amico2, Lisa A Mielke3, Francisca F Almeida2, Andrew J Kueh2, Ross A Dickins4, Gabrielle T Belz2, Shalin H Naik2, Andrew M Lew5, Phillipe Bouillet2, Marco J Herold2, Gordon K Smyth6, Lynn M Corcoran2, Stephen L Nutt7.
Abstract
Dendritic cells (DCs) are can be broadly divided into conventional (cDC) and plasmacytoid (pDC) subsets. Despite the importance of this lineage diversity, its genetic basis is not fully understood. We found that conditional ablation of the Ets-family transcription factor PU.1 in DC-restricted progenitors led to increased pDC production at the expense of cDCs. PU.1 controlled many of the cardinal functions of DCs, such as antigen presentation by cDCs and type I interferon production by pDCs. Conditional ablation of PU.1 de-repressed the pDC transcriptional signature in cDCs. The combination of genome-wide mapping of PU.1 binding and gene expression analysis revealed a key role for PU.1 in maintaining cDC identity through the induction of the transcriptional regulator DC-SCRIPT. PU.1 activated DC-SCRIPT expression, which in turn promoted cDC formation, particularly of cDC1s, and repressed pDC development. Thus, cDC identity is regulated by a transcriptional node requiring PU.1 and DC-SCRIPT.Entities:
Keywords: DC-SCRIPT; PU.1; cell differentiation; dendritic cell; plasmacytoid dendritic cell; transcription factor
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Year: 2019 PMID： 30611612 DOI： 10.1016/j.immuni.2018.11.010
Source DB: PubMed Journal: Immunity ISSN： 1074-7613 Impact factor: 31.745