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How Lipid-Specific T Cells Become Effectors: The Differentiation of iNKT Subsets

In contrast to peptide-recognizing T cells, invariant natural killer T (iNKT) cells express a semi-invariant T cell receptor that specifically recognizes self- or foreign-lipids presented by CD1d molecules. There are three major functionally distinct effector states for iNKT cells. Owning to these i...

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Detalles Bibliográficos
Autores principales: Wang, Haiguang, Hogquist, Kristin A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028555/
https://www.ncbi.nlm.nih.gov/pubmed/29997620
http://dx.doi.org/10.3389/fimmu.2018.01450
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author Wang, Haiguang
Hogquist, Kristin A.
author_facet Wang, Haiguang
Hogquist, Kristin A.
author_sort Wang, Haiguang
collection PubMed
description In contrast to peptide-recognizing T cells, invariant natural killer T (iNKT) cells express a semi-invariant T cell receptor that specifically recognizes self- or foreign-lipids presented by CD1d molecules. There are three major functionally distinct effector states for iNKT cells. Owning to these innate-like effector states, iNKT cells have been implicated in early protective immunity against pathogens. Yet, growing evidence suggests that iNKT cells play a role in tissue homeostasis as well. In this review, we discuss current knowledge about the underlying mechanisms that regulate the effector states of iNKT subsets, with a highlight on the roles of a variety of transcription factors and describe how each subset influences different facets of thymus homeostasis.
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spelling pubmed-60285552018-07-11 How Lipid-Specific T Cells Become Effectors: The Differentiation of iNKT Subsets Wang, Haiguang Hogquist, Kristin A. Front Immunol Immunology In contrast to peptide-recognizing T cells, invariant natural killer T (iNKT) cells express a semi-invariant T cell receptor that specifically recognizes self- or foreign-lipids presented by CD1d molecules. There are three major functionally distinct effector states for iNKT cells. Owning to these innate-like effector states, iNKT cells have been implicated in early protective immunity against pathogens. Yet, growing evidence suggests that iNKT cells play a role in tissue homeostasis as well. In this review, we discuss current knowledge about the underlying mechanisms that regulate the effector states of iNKT subsets, with a highlight on the roles of a variety of transcription factors and describe how each subset influences different facets of thymus homeostasis. Frontiers Media S.A. 2018-06-26 /pmc/articles/PMC6028555/ /pubmed/29997620 http://dx.doi.org/10.3389/fimmu.2018.01450 Text en Copyright © 2018 Wang and Hogquist. 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 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
Wang, Haiguang
Hogquist, Kristin A.
How Lipid-Specific T Cells Become Effectors: The Differentiation of iNKT Subsets
title How Lipid-Specific T Cells Become Effectors: The Differentiation of iNKT Subsets
title_full How Lipid-Specific T Cells Become Effectors: The Differentiation of iNKT Subsets
title_fullStr How Lipid-Specific T Cells Become Effectors: The Differentiation of iNKT Subsets
title_full_unstemmed How Lipid-Specific T Cells Become Effectors: The Differentiation of iNKT Subsets
title_short How Lipid-Specific T Cells Become Effectors: The Differentiation of iNKT Subsets
title_sort how lipid-specific t cells become effectors: the differentiation of inkt subsets
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028555/
https://www.ncbi.nlm.nih.gov/pubmed/29997620
http://dx.doi.org/10.3389/fimmu.2018.01450
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