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Recent advances in iNKT cell development

Recent studies suggest that murine invariant natural killer T (iNKT) cell development culminates in three terminally differentiated iNKT cell subsets denoted as NKT1, 2, and 17 cells. Although these studies corroborate the significance of the subset division model, less is known about the factors dr...

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Detalles Bibliográficos
Autores principales: Hogquist, Kristin, Georgiev, Hristo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7043113/
https://www.ncbi.nlm.nih.gov/pubmed/32148771
http://dx.doi.org/10.12688/f1000research.21378.1
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author Hogquist, Kristin
Georgiev, Hristo
author_facet Hogquist, Kristin
Georgiev, Hristo
author_sort Hogquist, Kristin
collection PubMed
description Recent studies suggest that murine invariant natural killer T (iNKT) cell development culminates in three terminally differentiated iNKT cell subsets denoted as NKT1, 2, and 17 cells. Although these studies corroborate the significance of the subset division model, less is known about the factors driving subset commitment in iNKT cell progenitors. In this review, we discuss the latest findings in iNKT cell development, focusing in particular on how T-cell receptor signal strength steers iNKT cell progenitors toward specific subsets and how early progenitor cells can be identified. In addition, we will discuss the essential factors for their sustenance and functionality. A picture is emerging wherein the majority of thymic iNKT cells are mature effector cells retained in the organ rather than developing precursors.
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spelling pubmed-70431132020-03-05 Recent advances in iNKT cell development Hogquist, Kristin Georgiev, Hristo F1000Res Review Recent studies suggest that murine invariant natural killer T (iNKT) cell development culminates in three terminally differentiated iNKT cell subsets denoted as NKT1, 2, and 17 cells. Although these studies corroborate the significance of the subset division model, less is known about the factors driving subset commitment in iNKT cell progenitors. In this review, we discuss the latest findings in iNKT cell development, focusing in particular on how T-cell receptor signal strength steers iNKT cell progenitors toward specific subsets and how early progenitor cells can be identified. In addition, we will discuss the essential factors for their sustenance and functionality. A picture is emerging wherein the majority of thymic iNKT cells are mature effector cells retained in the organ rather than developing precursors. F1000 Research Limited 2020-02-20 /pmc/articles/PMC7043113/ /pubmed/32148771 http://dx.doi.org/10.12688/f1000research.21378.1 Text en Copyright: © 2020 Hogquist K and Georgiev H http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Hogquist, Kristin
Georgiev, Hristo
Recent advances in iNKT cell development
title Recent advances in iNKT cell development
title_full Recent advances in iNKT cell development
title_fullStr Recent advances in iNKT cell development
title_full_unstemmed Recent advances in iNKT cell development
title_short Recent advances in iNKT cell development
title_sort recent advances in inkt cell development
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7043113/
https://www.ncbi.nlm.nih.gov/pubmed/32148771
http://dx.doi.org/10.12688/f1000research.21378.1
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