Cargando…

CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells

CD161 is a C-type lectin-like receptor expressed on the majority of natural killer (NK) cells; however, the significance of CD161 expression on NK cells has not been comprehensively investigated. Recently, we found that CD161 expression identifies a transcriptional and innate functional phenotype th...

Descripción completa

Detalles Bibliográficos
Autores principales: Kurioka, Ayako, Cosgrove, Cormac, Simoni, Yannick, van Wilgenburg, Bonnie, Geremia, Alessandra, Björkander, Sophia, Sverremark-Ekström, Eva, Thurnheer, Christine, Günthard, Huldrych F., Khanna, Nina, Walker, Lucy Jane, Arancibia-Cárcamo, Carolina V., Newell, Evan W., Willberg, Christian B., Klenerman, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900032/
https://www.ncbi.nlm.nih.gov/pubmed/29686665
http://dx.doi.org/10.3389/fimmu.2018.00486
_version_ 1783314346613407744
author Kurioka, Ayako
Cosgrove, Cormac
Simoni, Yannick
van Wilgenburg, Bonnie
Geremia, Alessandra
Björkander, Sophia
Sverremark-Ekström, Eva
Thurnheer, Christine
Günthard, Huldrych F.
Khanna, Nina
Walker, Lucy Jane
Arancibia-Cárcamo, Carolina V.
Newell, Evan W.
Willberg, Christian B.
Klenerman, Paul
author_facet Kurioka, Ayako
Cosgrove, Cormac
Simoni, Yannick
van Wilgenburg, Bonnie
Geremia, Alessandra
Björkander, Sophia
Sverremark-Ekström, Eva
Thurnheer, Christine
Günthard, Huldrych F.
Khanna, Nina
Walker, Lucy Jane
Arancibia-Cárcamo, Carolina V.
Newell, Evan W.
Willberg, Christian B.
Klenerman, Paul
author_sort Kurioka, Ayako
collection PubMed
description CD161 is a C-type lectin-like receptor expressed on the majority of natural killer (NK) cells; however, the significance of CD161 expression on NK cells has not been comprehensively investigated. Recently, we found that CD161 expression identifies a transcriptional and innate functional phenotype that is shared across various T cell populations. Using mass cytometry and microarray experiments, we demonstrate that this functional phenotype extends to NK cells. CD161 marks NK cells that have retained the ability to respond to innate cytokines during their differentiation, and is lost upon cytomegalovirus-induced maturation in both healthy and human immunodeficiency virus (HIV)-infected patients. These pro-inflammatory NK cells are present in the inflamed lamina propria where they are enriched for integrin CD103 expression. Thus, CD161 expression identifies NK cells that may contribute to inflammatory disease pathogenesis and correlates with an innate responsiveness to cytokines in both T and NK cells.
format Online
Article
Text
id pubmed-5900032
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-59000322018-04-23 CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells Kurioka, Ayako Cosgrove, Cormac Simoni, Yannick van Wilgenburg, Bonnie Geremia, Alessandra Björkander, Sophia Sverremark-Ekström, Eva Thurnheer, Christine Günthard, Huldrych F. Khanna, Nina Walker, Lucy Jane Arancibia-Cárcamo, Carolina V. Newell, Evan W. Willberg, Christian B. Klenerman, Paul Front Immunol Immunology CD161 is a C-type lectin-like receptor expressed on the majority of natural killer (NK) cells; however, the significance of CD161 expression on NK cells has not been comprehensively investigated. Recently, we found that CD161 expression identifies a transcriptional and innate functional phenotype that is shared across various T cell populations. Using mass cytometry and microarray experiments, we demonstrate that this functional phenotype extends to NK cells. CD161 marks NK cells that have retained the ability to respond to innate cytokines during their differentiation, and is lost upon cytomegalovirus-induced maturation in both healthy and human immunodeficiency virus (HIV)-infected patients. These pro-inflammatory NK cells are present in the inflamed lamina propria where they are enriched for integrin CD103 expression. Thus, CD161 expression identifies NK cells that may contribute to inflammatory disease pathogenesis and correlates with an innate responsiveness to cytokines in both T and NK cells. Frontiers Media S.A. 2018-04-09 /pmc/articles/PMC5900032/ /pubmed/29686665 http://dx.doi.org/10.3389/fimmu.2018.00486 Text en Copyright © 2018 Kurioka, Cosgrove, Simoni, van Wilgenburg, Geremia, Björkander, Sverremark-Ekström, Thurnheer, Günthard, Khanna, The Swiss HIV Cohort Study, Oxford IBD Cohort Investigators, Walker, Arancibia-Cárcamo, Newell, Willberg and Klenerman. 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
Kurioka, Ayako
Cosgrove, Cormac
Simoni, Yannick
van Wilgenburg, Bonnie
Geremia, Alessandra
Björkander, Sophia
Sverremark-Ekström, Eva
Thurnheer, Christine
Günthard, Huldrych F.
Khanna, Nina
Walker, Lucy Jane
Arancibia-Cárcamo, Carolina V.
Newell, Evan W.
Willberg, Christian B.
Klenerman, Paul
CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells
title CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells
title_full CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells
title_fullStr CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells
title_full_unstemmed CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells
title_short CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells
title_sort cd161 defines a functionally distinct subset of pro-inflammatory natural killer cells
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900032/
https://www.ncbi.nlm.nih.gov/pubmed/29686665
http://dx.doi.org/10.3389/fimmu.2018.00486
work_keys_str_mv AT kuriokaayako cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT cosgrovecormac cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT simoniyannick cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT vanwilgenburgbonnie cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT geremiaalessandra cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT bjorkandersophia cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT sverremarkekstromeva cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT thurnheerchristine cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT gunthardhuldrychf cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT khannanina cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT walkerlucyjane cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT arancibiacarcamocarolinav cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT newellevanw cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT willbergchristianb cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells
AT klenermanpaul cd161definesafunctionallydistinctsubsetofproinflammatorynaturalkillercells