| Literature DB >> 31882362 |
Chao Zhong1, Mingzhu Zheng2, Kairong Cui3, Andrew J Martins2, Gangqing Hu4, Dan Li5, Lino Tessarollo6, Serguei Kozlov7, Jonathan R Keller8, John S Tsang2, Keji Zhao3, Jinfang Zhu9.
Abstract
Lymphoid tissue inducer (LTi) cells are regarded as a subset of innate lymphoid cells (ILCs). However, these cells are not derived from the ILC common progenitor, which generates other ILC subsets and is defined by the expression of the transcription factor PLZF. Here, we examined transcription factor(s) determining the fate of LTi progenitors versus non-LTi ILC progenitors. Conditional deletion of Gata3 resulted in the loss of PLZF+ non-LTi progenitors but not the LTi progenitors that expressed the transcription factor RORγt. Consistently, PLZF+ non-LTi progenitors expressed high amounts of GATA3, whereas GATA3 expression was low in RORγt+ LTi progenitors. The generation of both progenitors required the transcriptional regulator Id2, which defines the common helper-like innate lymphoid progenitor (ChILP), but not cytokine signaling. Nevertheless, low GATA3 expression was necessary for the generation of functionally mature LTi cells. Thus, differential expression of GATA3 determines the fates and functions of distinct ILC progenitors.Entities:
Keywords: cell fate bifurcation; gene expression; innate lymphoid cell; lineage commitment; lymphocyte development; lymphoid tissue inducer; lymphopoiesis; progenitor heterogeneity; transcription factor; transcriptional regulation
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Year: 2019 PMID: 31882362 PMCID: PMC6962539 DOI: 10.1016/j.immuni.2019.12.001
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745