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New Molecular Insights into Immune Cell Development

Authors :
Ana Cumano
Rachel Golub
Claire Berthault
Antonio Bandeira
Cyrille Ramond
Maxime Petit
Pablo Pereira
Cellule Pasteur
Université Paris Diderot - Paris 7 (UPD7)-PRES Sorbonne Paris Cité
Lymphopoïèse (Lymphopoïèse (UMR_1223 / U1223 / U-Pasteur_4))
Institut Pasteur [Paris] (IP)-Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM)
This work was financed by the Pasteur Institute, INSERM, ANR (grant Twothyme) for A.C. and (grant Myeloten) R.G. and by REVIVE Future Investment Program and Pasteur-Weizmann Foundation through grants to A.C. We apologize to all colleagues that contributed to the field and whose work could not be cited here due to limitation in space availability.
We thank members of the A.C. laboratory for many fruitful discussions.
ANR-14-CE11-0022,Twothyme,Deux progéniteurs hématopoïétiques différents établissent le compartiment de lymphocytes T: tester un nouveau paradigme du développement T.(2014)
ANR-13-ISV1-0003,MYELOTEN,DEREGULATION DE L'HEMATOPOIESE PAR LA SUREXPRESSION DE L'INTERLEUKINE-10 : IMPLICATIONS DANS LE DEVELOPPEMENT DE PATHOLOGIES HEMATOLOGIQUES(2013)
Vougny, Marie-Christine
Appel à projets générique - Deux progéniteurs hématopoïétiques différents établissent le compartiment de lymphocytes T: tester un nouveau paradigme du développement T. - - Twothyme2014 - ANR-14-CE11-0022 - Appel à projets générique - VALID
Blanc – Accords bilatéraux 2013 - DEREGULATION DE L'HEMATOPOIESE PAR LA SUREXPRESSION DE L'INTERLEUKINE-10 : IMPLICATIONS DANS LE DEVELOPPEMENT DE PATHOLOGIES HEMATOLOGIQUES - - MYELOTEN2013 - ANR-13-ISV1-0003 - Blanc – Accords bilatéraux 2013 - VALID
Institut Pasteur [Paris]-Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Source :
Annual Review of Immunology, Annual Review of Immunology, 2019, 37 (1), pp.497-519. ⟨10.1146/annurev-immunol-042718-041319⟩, Annual Review of Immunology, Annual Reviews, 2019, 37 (1), pp.497-519. ⟨10.1146/annurev-immunol-042718-041319⟩
Publication Year :
2019
Publisher :
HAL CCSD, 2019.

Abstract

International audience; 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.

Details

Language :
English
ISSN :
07320582
Database :
OpenAIRE
Journal :
Annual Review of Immunology, Annual Review of Immunology, 2019, 37 (1), pp.497-519. ⟨10.1146/annurev-immunol-042718-041319⟩, Annual Review of Immunology, Annual Reviews, 2019, 37 (1), pp.497-519. ⟨10.1146/annurev-immunol-042718-041319⟩
Accession number :
edsair.doi.dedup.....d647dc479cf8861d0699337c24bf7811