The basic leucine zipper transcription factor NFIL3 directs the development of a common innate lymphoid cell precursor

Xiaofei Yu, Yuhao Wang, Mi Deng Ph.D., Yun Li, Kelly A. Ruhn, Chengcheng Zhang, Lora V Hooper

Research output: Contribution to journalArticle

122 Citations (Scopus)

Abstract

Innate lymphoid cells (ILCs) are recently identified lymphocytes that limit infection and promote tissue repair at mucosal surfaces. However, the pathways underlying ILC development remain unclear. Here we show that the transcription factor NFIL3 directs the development of a committed bone marrow precursor that differentiates into all known ILC lineages. NFIL3 was required in the common lymphoid progenitor (CLP), and was essential for the differentiation of αLP, a bone marrow cell population that gives rise to all known ILC lineages. Clonal differentiation studies revealed that CXCR6(+) cells within the αLP population differentiate into all ILC lineages but not T- and B-cells. We further show that NFIL3 governs ILC development by directly regulating expression of the transcription factor TOX. These findings establish that NFIL3 directs the differentiation of a committed ILC precursor that gives rise to all ILC lineages and provide insight into the defining role of NFIL3 in ILC development.

Original languageEnglish (US)
JournaleLife
Volume3
DOIs
StatePublished - Oct 13 2014

Fingerprint

Basic-Leucine Zipper Transcription Factors
Bone
Transcription Factors
Cells
Lymphocytes
Cell Lineage
Repair
Tissue
Lymphoid Progenitor Cells
Bone Marrow Cells
Population
B-Lymphocytes
Bone Marrow

Keywords

  • bone marrow progenitor
  • developmental biology
  • immunology
  • innate immunity
  • innate lymphoid cells
  • intestinal immunity
  • mouse
  • stem cell
  • stem cells

ASJC Scopus subject areas

  • Neuroscience(all)
  • Medicine(all)
  • Immunology and Microbiology(all)
  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

The basic leucine zipper transcription factor NFIL3 directs the development of a common innate lymphoid cell precursor. / Yu, Xiaofei; Wang, Yuhao; Deng Ph.D., Mi; Li, Yun; Ruhn, Kelly A.; Zhang, Chengcheng; Hooper, Lora V.

In: eLife, Vol. 3, 13.10.2014.

Research output: Contribution to journalArticle

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AU - Ruhn, Kelly A.

AU - Zhang, Chengcheng

AU - Hooper, Lora V

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N2 - Innate lymphoid cells (ILCs) are recently identified lymphocytes that limit infection and promote tissue repair at mucosal surfaces. However, the pathways underlying ILC development remain unclear. Here we show that the transcription factor NFIL3 directs the development of a committed bone marrow precursor that differentiates into all known ILC lineages. NFIL3 was required in the common lymphoid progenitor (CLP), and was essential for the differentiation of αLP, a bone marrow cell population that gives rise to all known ILC lineages. Clonal differentiation studies revealed that CXCR6(+) cells within the αLP population differentiate into all ILC lineages but not T- and B-cells. We further show that NFIL3 governs ILC development by directly regulating expression of the transcription factor TOX. These findings establish that NFIL3 directs the differentiation of a committed ILC precursor that gives rise to all ILC lineages and provide insight into the defining role of NFIL3 in ILC development.

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