| Literature DB >> 23601684 |
Qi Yang1, Laurel A Monticelli, Steven A Saenz, Anthony Wei-Shine Chi, Gregory F Sonnenberg, Jiangbo Tang, Maria Elena De Obaldia, Will Bailis, Jerrod L Bryson, Kristin Toscano, Jian Huang, Angela Haczku, Warren S Pear, David Artis, Avinash Bhandoola.
Abstract
Group 2 innate lymphoid cells (ILC2) are innate lymphocytes that confer protective type 2 immunity during helminth infection and are also involved in allergic airway inflammation. Here we report that ILC2 development required T cell factor 1 (TCF-1, the product of the Tcf7 gene), a transcription factor also implicated in T cell lineage specification. Tcf7(-/-) mice lack ILC2, and were unable to mount ILC2-mediated innate type 2 immune responses. Forced expression of TCF-1 in bone marrow progenitors partially bypassed the requirement for Notch signaling in the generation of ILC2 in vivo. TCF-1 acted through both GATA-3-dependent and GATA-3-independent pathways to promote the generation of ILC2. These results are reminiscent of the critical roles of TCF-1 in early T cell development. Hence, transcription factors that underlie early steps of T cell development are also implicated in the development of innate lymphoid cells.Entities:
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Year: 2013 PMID: 23601684 PMCID: PMC4029843 DOI: 10.1016/j.immuni.2012.12.003
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745