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Mapping of NKp46(+) Cells in Healthy Human Lymphoid and Non-Lymphoid Tissues

Understanding Natural Killer (NK) cell anatomical distribution is key to dissect the role of these unconventional lymphocytes in physiological and disease conditions. In mouse, NK cells have been detected in various lymphoid and non-lymphoid organs, while in humans the current knowledge of NK cell d...

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Autores principales: Tomasello, Elena, Yessaad, Nadia, Gregoire, Emilie, Hudspeth, Kelly, Luci, Carmelo, Mavilio, Domenico, Hardwigsen, Jean, Vivier, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3501723/
https://www.ncbi.nlm.nih.gov/pubmed/23181063
http://dx.doi.org/10.3389/fimmu.2012.00344
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author Tomasello, Elena
Yessaad, Nadia
Gregoire, Emilie
Hudspeth, Kelly
Luci, Carmelo
Mavilio, Domenico
Hardwigsen, Jean
Vivier, Eric
author_facet Tomasello, Elena
Yessaad, Nadia
Gregoire, Emilie
Hudspeth, Kelly
Luci, Carmelo
Mavilio, Domenico
Hardwigsen, Jean
Vivier, Eric
author_sort Tomasello, Elena
collection PubMed
description Understanding Natural Killer (NK) cell anatomical distribution is key to dissect the role of these unconventional lymphocytes in physiological and disease conditions. In mouse, NK cells have been detected in various lymphoid and non-lymphoid organs, while in humans the current knowledge of NK cell distribution at steady state is mainly restricted to lymphoid tissues. The translation to humans of findings obtained in mice is facilitated by the identification of NK cell markers conserved between these two species. The Natural Cytotoxicity Receptor (NCR) NKp46 is a marker of the NK cell lineage evolutionary conserved in mammals. In mice, NKp46 is also present on rare T cell subsets and on a subset of gut Innate Lymphoid Cells (ILCs) expressing the retinoic acid receptor-related orphan receptor γt (RORγt) transcription factor. Here, we documented the distribution and the phenotype of human NKp46(+) cells in lymphoid and non-lymphoid tissues isolated from healthy donors. Human NKp46(+) cells were found in splenic red pulp, in lymph nodes, in lungs, and gut lamina propria, thus mirroring mouse NKp46(+) cell distribution. We also identified a novel cell subset of CD56(dim)NKp46(low) cells that includes RORγt(+) ILCs with a lineage(−)CD94(−)CD117(bright)CD127(bright) phenotype. The use of NKp46 thus contributes to establish the basis for analyzing quantitative and qualitative changes of NK cell and ILC subsets in human diseases.
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spelling pubmed-35017232012-11-23 Mapping of NKp46(+) Cells in Healthy Human Lymphoid and Non-Lymphoid Tissues Tomasello, Elena Yessaad, Nadia Gregoire, Emilie Hudspeth, Kelly Luci, Carmelo Mavilio, Domenico Hardwigsen, Jean Vivier, Eric Front Immunol Immunology Understanding Natural Killer (NK) cell anatomical distribution is key to dissect the role of these unconventional lymphocytes in physiological and disease conditions. In mouse, NK cells have been detected in various lymphoid and non-lymphoid organs, while in humans the current knowledge of NK cell distribution at steady state is mainly restricted to lymphoid tissues. The translation to humans of findings obtained in mice is facilitated by the identification of NK cell markers conserved between these two species. The Natural Cytotoxicity Receptor (NCR) NKp46 is a marker of the NK cell lineage evolutionary conserved in mammals. In mice, NKp46 is also present on rare T cell subsets and on a subset of gut Innate Lymphoid Cells (ILCs) expressing the retinoic acid receptor-related orphan receptor γt (RORγt) transcription factor. Here, we documented the distribution and the phenotype of human NKp46(+) cells in lymphoid and non-lymphoid tissues isolated from healthy donors. Human NKp46(+) cells were found in splenic red pulp, in lymph nodes, in lungs, and gut lamina propria, thus mirroring mouse NKp46(+) cell distribution. We also identified a novel cell subset of CD56(dim)NKp46(low) cells that includes RORγt(+) ILCs with a lineage(−)CD94(−)CD117(bright)CD127(bright) phenotype. The use of NKp46 thus contributes to establish the basis for analyzing quantitative and qualitative changes of NK cell and ILC subsets in human diseases. Frontiers Media S.A. 2012-11-20 /pmc/articles/PMC3501723/ /pubmed/23181063 http://dx.doi.org/10.3389/fimmu.2012.00344 Text en Copyright © 2012 Tomasello, Yessaad, Gregoire, Hudspeth, Luci, Mavilio, Hardwigsen and Vivier. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Immunology
Tomasello, Elena
Yessaad, Nadia
Gregoire, Emilie
Hudspeth, Kelly
Luci, Carmelo
Mavilio, Domenico
Hardwigsen, Jean
Vivier, Eric
Mapping of NKp46(+) Cells in Healthy Human Lymphoid and Non-Lymphoid Tissues
title Mapping of NKp46(+) Cells in Healthy Human Lymphoid and Non-Lymphoid Tissues
title_full Mapping of NKp46(+) Cells in Healthy Human Lymphoid and Non-Lymphoid Tissues
title_fullStr Mapping of NKp46(+) Cells in Healthy Human Lymphoid and Non-Lymphoid Tissues
title_full_unstemmed Mapping of NKp46(+) Cells in Healthy Human Lymphoid and Non-Lymphoid Tissues
title_short Mapping of NKp46(+) Cells in Healthy Human Lymphoid and Non-Lymphoid Tissues
title_sort mapping of nkp46(+) cells in healthy human lymphoid and non-lymphoid tissues
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3501723/
https://www.ncbi.nlm.nih.gov/pubmed/23181063
http://dx.doi.org/10.3389/fimmu.2012.00344
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