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Porcine Plasmacytoid Dendritic Cells Are Unique in Their Expression of a Functional NKp46 Receptor

The activating receptor NKp46 shows a unique expression pattern on porcine leukocytes. We showed already that in swine not all NK cells express NKp46 and that CD3(+)NKp46(+) lymphocytes form a T-cell subset with unique functional properties. Here we demonstrate the expression of NKp46 on CD4(high)CD...

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Autores principales: Mair, Kerstin H., Stadler, Maria, Razavi, Mahsa Adib, Saalmüller, Armin, Gerner, Wilhelm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8970115/
https://www.ncbi.nlm.nih.gov/pubmed/35371050
http://dx.doi.org/10.3389/fimmu.2022.822258
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author Mair, Kerstin H.
Stadler, Maria
Razavi, Mahsa Adib
Saalmüller, Armin
Gerner, Wilhelm
author_facet Mair, Kerstin H.
Stadler, Maria
Razavi, Mahsa Adib
Saalmüller, Armin
Gerner, Wilhelm
author_sort Mair, Kerstin H.
collection PubMed
description The activating receptor NKp46 shows a unique expression pattern on porcine leukocytes. We showed already that in swine not all NK cells express NKp46 and that CD3(+)NKp46(+) lymphocytes form a T-cell subset with unique functional properties. Here we demonstrate the expression of NKp46 on CD4(high)CD14(-)CD172a(+) porcine plasmacytoid dendritic cells (pDCs). Multicolor flow cytometry analyses revealed that the vast majority of porcine pDCs (94.2% ± 4) express NKp46 ex vivo and have an increased expression on the single-cell level compared to NK cells. FSC/SSC(high)CD4(high)NKp46(+) cells produced high levels of IFN-α after CpG ODN 2216 stimulation, a hallmark of pDC function. Following receptor triggering with plate-bound monoclonal antibodies against NKp46, phosphorylation of signaling molecules downstream of NKp46 was analyzed in pDCs and NK cells. Comparable to NK cells, NKp46 triggering led to an upregulation of the phosphorylated ribosomal protein S6 (pS6) in pDCs, indicating an active signaling pathway of NKp46 in porcine pDCs. Nevertheless, a defined effector function of the NK-associated receptor on porcine pDCs could not be demonstrated yet. NKp46-mediated cytotoxicity, as shown for NK cells, does not seem to occur, as NKp46(+) pDCs did not express perforin. Yet, NKp46 triggering seems to contribute to cytokine production in porcine pDCs, as induction of TNF-α was observed in a small pDC subset after NKp46 cross-linking. To our knowledge, this is the first report on NKp46 expression on pDCs in a mammalian species, showing that this receptor contributes to pDC activation and function.
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spelling pubmed-89701152022-04-01 Porcine Plasmacytoid Dendritic Cells Are Unique in Their Expression of a Functional NKp46 Receptor Mair, Kerstin H. Stadler, Maria Razavi, Mahsa Adib Saalmüller, Armin Gerner, Wilhelm Front Immunol Immunology The activating receptor NKp46 shows a unique expression pattern on porcine leukocytes. We showed already that in swine not all NK cells express NKp46 and that CD3(+)NKp46(+) lymphocytes form a T-cell subset with unique functional properties. Here we demonstrate the expression of NKp46 on CD4(high)CD14(-)CD172a(+) porcine plasmacytoid dendritic cells (pDCs). Multicolor flow cytometry analyses revealed that the vast majority of porcine pDCs (94.2% ± 4) express NKp46 ex vivo and have an increased expression on the single-cell level compared to NK cells. FSC/SSC(high)CD4(high)NKp46(+) cells produced high levels of IFN-α after CpG ODN 2216 stimulation, a hallmark of pDC function. Following receptor triggering with plate-bound monoclonal antibodies against NKp46, phosphorylation of signaling molecules downstream of NKp46 was analyzed in pDCs and NK cells. Comparable to NK cells, NKp46 triggering led to an upregulation of the phosphorylated ribosomal protein S6 (pS6) in pDCs, indicating an active signaling pathway of NKp46 in porcine pDCs. Nevertheless, a defined effector function of the NK-associated receptor on porcine pDCs could not be demonstrated yet. NKp46-mediated cytotoxicity, as shown for NK cells, does not seem to occur, as NKp46(+) pDCs did not express perforin. Yet, NKp46 triggering seems to contribute to cytokine production in porcine pDCs, as induction of TNF-α was observed in a small pDC subset after NKp46 cross-linking. To our knowledge, this is the first report on NKp46 expression on pDCs in a mammalian species, showing that this receptor contributes to pDC activation and function. Frontiers Media S.A. 2022-03-11 /pmc/articles/PMC8970115/ /pubmed/35371050 http://dx.doi.org/10.3389/fimmu.2022.822258 Text en Copyright © 2022 Mair, Stadler, Razavi, Saalmüller and Gerner 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(s) 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
Mair, Kerstin H.
Stadler, Maria
Razavi, Mahsa Adib
Saalmüller, Armin
Gerner, Wilhelm
Porcine Plasmacytoid Dendritic Cells Are Unique in Their Expression of a Functional NKp46 Receptor
title Porcine Plasmacytoid Dendritic Cells Are Unique in Their Expression of a Functional NKp46 Receptor
title_full Porcine Plasmacytoid Dendritic Cells Are Unique in Their Expression of a Functional NKp46 Receptor
title_fullStr Porcine Plasmacytoid Dendritic Cells Are Unique in Their Expression of a Functional NKp46 Receptor
title_full_unstemmed Porcine Plasmacytoid Dendritic Cells Are Unique in Their Expression of a Functional NKp46 Receptor
title_short Porcine Plasmacytoid Dendritic Cells Are Unique in Their Expression of a Functional NKp46 Receptor
title_sort porcine plasmacytoid dendritic cells are unique in their expression of a functional nkp46 receptor
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8970115/
https://www.ncbi.nlm.nih.gov/pubmed/35371050
http://dx.doi.org/10.3389/fimmu.2022.822258
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