Development and differentiation of early innate lymphoid progenitors
Open accessAbstract
Early innate lymphoid progenitors (EILPs) have recently been identified in mouse adult bone marrow as a multipotential progenitor population specified toward innate lymphoid cell (ILC) lineages, but their relationship with other described ILC progenitors is still unclear. In this study, we examine the progenitor–successor relationships between EILPs, all-lymphoid progenitors (ALPs), and ILC precursors (ILCps). Functional, bioinformatic, phenotypical, and genetic approaches collectively establish EILPs as an intermediate progenitor between ALPs and ILCps. Our work additionally provides new candidate regulators of ILC development and clearly defines the stage of requirement of transcription factors key for early ILC development.
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The innate lymphoid cell developmental program appears to resemble the intrathymic T-cell program in many respects.
“So far the innate lymphoid cell developmental program in particular appears to resemble the intrathymic T-cell program in many respects (154–157), enough to raise the question of what makes T-cell precursors wait to activate genes like Tcf7 and Gata3 until they reach the thymus.”
From Mechanisms of Action of Hematopoietic Transcription Factor PU.1 in Initiation of T-Cell Development (2019) · cites this paper as [157]
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- Authors
- Harly, C., Cam, M., Kaye, J., & Bhandoola, A.
- Affiliations
- National Institutes of Health (US)
- Cedars-Sinai Medical Center (US)
- Corresponding author
- Bhandoola, Avinash
- Venue
- Journal of Experimental Medicine
- Publisher
- Rockefeller University Press
- Published
- 2017-11-28
- Volume
- 215
- Issue
- 1
- Pages
- 249-262
- ISSN
- 0022-1007 (ISSN-L)
- 1540-9538
- PMC
- PMC5748853
- OpenAlex
- W2769255069
- Cited by
- 125
- References
- 54
- Citations by year
- 2026: 13 · 2025: 10 · 2024: 14 · 2023: 9 · 2022: 18 · 2021: 9 · 2020: 19 · 2019: 25 · 2018: 8
- FWCI
- 6.44
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- The Journal of Experimental Medicine (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- HAL (submittedVersion, other-oa)
- Funders
- National Cancer Institute
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Mast cells and histamine
- Keywords
- innate lymphoid cells, progenitor cell differentiation, bone marrow, transcription factors, multipotent progenitors
- MeSH terms
- Animals, Bone Marrow Cells, Cell Differentiation, Immunity, Innate, Mice, Transgenic, Phenotype, Biomarkers, Immunophenotyping, Lymphocyte Subsets, Cytokines, Mice, Knockout, Gene Expression Profiling, GATA3 Transcription Factor, Mice, Lymphoid Progenitor Cells
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