| Literature DB >> 31026413 |
Ana Cumano1,2, Claire Berthault1,2, Cyrille Ramond1, Maxime Petit1,2, Rachel Golub1,2, Antonio Bandeira1,2, Pablo Pereira1,2.
Abstract
During development innate lymphoid cells and specialized lymphocyte subsets colonize peripheral tissues, where they contribute to organogenesis and later constitute the first line of protection while maintaining tissue homeostasis. A few of these subsets are produced only during embryonic development and remain in the tissues throughout life. They are generated through a unique developmental program initiated in lympho-myeloid-primed progenitors, which lose myeloid and B cell potential. They either differentiate into innate lymphoid cells or migrate to the thymus to give rise to embryonic T cell receptor-invariant T cells. At later developmental stages, adaptive T lymphocytes are derived from lympho-myeloid progenitors that colonize the thymus, while lymphoid progenitors become specialized in the production of B cells. This sequence of events highlights the requirement for stratification in the establishment of immune functions that determine efficient seeding of peripheral tissues by a limited number of cells.Entities:
Keywords: fetal liver; innate lymphoid cells; lineage commitment; lymphoid progenitors; thymus-settling progenitors; transcriptional signatures
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Year: 2019 PMID: 31026413 DOI: 10.1146/annurev-immunol-042718-041319
Source DB: PubMed Journal: Annu Rev Immunol ISSN: 0732-0582 Impact factor: 28.527