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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2020
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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. |
format | Online Article Text |
id | pubmed-7043113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT hogquistkristin recentadvancesininktcelldevelopment AT georgievhristo recentadvancesininktcelldevelopment |