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Embryonic ILC-poiesis across tissues

The family of innate lymphoid cells (ILCs), consisting of Group 1 ILCs (natural killer cells and ILC1), ILC2, and ILC3, are critical effectors of innate immunity, inflammation, and homeostasis post-natally, but also exert essential functions before birth. Recent studies during critical developmental...

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Detalles Bibliográficos
Autores principales: Hernández-Torres, Daniela Carolina, Stehle, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807749/
https://www.ncbi.nlm.nih.gov/pubmed/36605193
http://dx.doi.org/10.3389/fimmu.2022.1040624
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author Hernández-Torres, Daniela Carolina
Stehle, Christina
author_facet Hernández-Torres, Daniela Carolina
Stehle, Christina
author_sort Hernández-Torres, Daniela Carolina
collection PubMed
description The family of innate lymphoid cells (ILCs), consisting of Group 1 ILCs (natural killer cells and ILC1), ILC2, and ILC3, are critical effectors of innate immunity, inflammation, and homeostasis post-natally, but also exert essential functions before birth. Recent studies during critical developmental periods in the embryo have hinted at complex waves of tissue colonization, and highlighted the breadth of multipotent and committed ILC progenitors from both classic fetal hematopoietic organs such as the liver, as well as tissue sites such as the lung, thymus, and intestine. Assessment of the mechanisms driving cell fate and function of the ILC family in the embryo will be vital to the understanding ILC biology throughout fetal life and beyond.
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spelling pubmed-98077492023-01-04 Embryonic ILC-poiesis across tissues Hernández-Torres, Daniela Carolina Stehle, Christina Front Immunol Immunology The family of innate lymphoid cells (ILCs), consisting of Group 1 ILCs (natural killer cells and ILC1), ILC2, and ILC3, are critical effectors of innate immunity, inflammation, and homeostasis post-natally, but also exert essential functions before birth. Recent studies during critical developmental periods in the embryo have hinted at complex waves of tissue colonization, and highlighted the breadth of multipotent and committed ILC progenitors from both classic fetal hematopoietic organs such as the liver, as well as tissue sites such as the lung, thymus, and intestine. Assessment of the mechanisms driving cell fate and function of the ILC family in the embryo will be vital to the understanding ILC biology throughout fetal life and beyond. Frontiers Media S.A. 2022-12-20 /pmc/articles/PMC9807749/ /pubmed/36605193 http://dx.doi.org/10.3389/fimmu.2022.1040624 Text en Copyright © 2022 Hernández-Torres and Stehle https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Hernández-Torres, Daniela Carolina
Stehle, Christina
Embryonic ILC-poiesis across tissues
title Embryonic ILC-poiesis across tissues
title_full Embryonic ILC-poiesis across tissues
title_fullStr Embryonic ILC-poiesis across tissues
title_full_unstemmed Embryonic ILC-poiesis across tissues
title_short Embryonic ILC-poiesis across tissues
title_sort embryonic ilc-poiesis across tissues
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807749/
https://www.ncbi.nlm.nih.gov/pubmed/36605193
http://dx.doi.org/10.3389/fimmu.2022.1040624
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