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Nat Immunol. 2011 Sep 11;12(10):949-58. doi: 10.1038/ni.2105.

Notch signaling is necessary for adult, but not fetal, development of RORγt(+) innate lymphoid cells.

Author information

1
Institut Pasteur, Unité de Lymphopoièse, Paris, France.

Abstract

The transcription factor RORγt is required for the development of several innate lymphoid populations, such as lymphoid tissue-inducer cells (LTi cells) and cells that secrete interleukin 17 (IL-17) or IL-22. The progenitor cells as well as the developmental stages that lead to the emergence of RORγt(+) innate lymphoid cells (ILCs) remain undefined. Here we identify the chemokine receptor CXCR6 as an additional marker of the development of ILCs and show that common lymphoid progenitors lost B cell and T cell potential as they successively acquired expression of the integrin α(4)β(7) and CXCR6. Whereas fetal RORγt(+) cells matured in the fetal liver environment, adult bone marrow-derived RORγt(+) ILCs matured outside the bone marrow, in a Notch2-dependent manner. Therefore, fetal and adult environments influence the differentiation of RORγt(+) cells differently.

PMID:
21909092
DOI:
10.1038/ni.2105
[Indexed for MEDLINE]

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