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Lymphocyte antigen 6 complex locus G6D downregulation is a novel parameter for functional impairment of neutrophils in aged mice
Immunological aging is a critical event that causes serious functional impairment in the innate immune system. However, the identification markers and parameters are still poorly understood in immunological aging of myeloid lineage cells. Here, we show that a downregulation of lymphocyte antigen 6 c...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647080/ https://www.ncbi.nlm.nih.gov/pubmed/36389807 http://dx.doi.org/10.3389/fimmu.2022.1001179 |
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author | Saito, Suguru Okuno, Alato Maekawa, Toshio Kobayashi, Ryoki Yamashita, Osamu Tsujimura, Noriyuki Inaba, Morihiko Kageyama, Yasushi Tsuji, Noriko M. |
author_facet | Saito, Suguru Okuno, Alato Maekawa, Toshio Kobayashi, Ryoki Yamashita, Osamu Tsujimura, Noriyuki Inaba, Morihiko Kageyama, Yasushi Tsuji, Noriko M. |
author_sort | Saito, Suguru |
collection | PubMed |
description | Immunological aging is a critical event that causes serious functional impairment in the innate immune system. However, the identification markers and parameters are still poorly understood in immunological aging of myeloid lineage cells. Here, we show that a downregulation of lymphocyte antigen 6 complex locus G6D (Ly-6G) observed in aged mouse neutrophils could serve as a novel marker for the prediction of age-associated functional impairment in the neutrophils. Ly-6G expression was significantly downregulated in the bone marrow (BM) neutrophils of aged mice compared to young mice confirmed by flow cytometry analysis. In vitro experiments using BM-isolated neutrophils showed significant downregulations in their activities, such as phagocytosis, reactive oxygen species (ROS) production, interleukin (IL)-1β production, neutrophil extracellular trap (NET) formation, and migration as well as bacterial clearance, in the aged mouse neutrophils compared to those of young mice counterparts. Interestingly, the magnitudes of functional parameters were strongly correlated with the Ly-6G expression in the neutrophils. Thus, our results suggest that downregulation of Ly-6G reflects the age-associated functional attenuation of the neutrophils. |
format | Online Article Text |
id | pubmed-9647080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96470802022-11-15 Lymphocyte antigen 6 complex locus G6D downregulation is a novel parameter for functional impairment of neutrophils in aged mice Saito, Suguru Okuno, Alato Maekawa, Toshio Kobayashi, Ryoki Yamashita, Osamu Tsujimura, Noriyuki Inaba, Morihiko Kageyama, Yasushi Tsuji, Noriko M. Front Immunol Immunology Immunological aging is a critical event that causes serious functional impairment in the innate immune system. However, the identification markers and parameters are still poorly understood in immunological aging of myeloid lineage cells. Here, we show that a downregulation of lymphocyte antigen 6 complex locus G6D (Ly-6G) observed in aged mouse neutrophils could serve as a novel marker for the prediction of age-associated functional impairment in the neutrophils. Ly-6G expression was significantly downregulated in the bone marrow (BM) neutrophils of aged mice compared to young mice confirmed by flow cytometry analysis. In vitro experiments using BM-isolated neutrophils showed significant downregulations in their activities, such as phagocytosis, reactive oxygen species (ROS) production, interleukin (IL)-1β production, neutrophil extracellular trap (NET) formation, and migration as well as bacterial clearance, in the aged mouse neutrophils compared to those of young mice counterparts. Interestingly, the magnitudes of functional parameters were strongly correlated with the Ly-6G expression in the neutrophils. Thus, our results suggest that downregulation of Ly-6G reflects the age-associated functional attenuation of the neutrophils. Frontiers Media S.A. 2022-10-27 /pmc/articles/PMC9647080/ /pubmed/36389807 http://dx.doi.org/10.3389/fimmu.2022.1001179 Text en Copyright © 2022 Saito, Okuno, Maekawa, Kobayashi, Yamashita, Tsujimura, Inaba, Kageyama and Tsuji 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 Saito, Suguru Okuno, Alato Maekawa, Toshio Kobayashi, Ryoki Yamashita, Osamu Tsujimura, Noriyuki Inaba, Morihiko Kageyama, Yasushi Tsuji, Noriko M. Lymphocyte antigen 6 complex locus G6D downregulation is a novel parameter for functional impairment of neutrophils in aged mice |
title | Lymphocyte antigen 6 complex locus G6D downregulation is a novel parameter for functional impairment of neutrophils in aged mice |
title_full | Lymphocyte antigen 6 complex locus G6D downregulation is a novel parameter for functional impairment of neutrophils in aged mice |
title_fullStr | Lymphocyte antigen 6 complex locus G6D downregulation is a novel parameter for functional impairment of neutrophils in aged mice |
title_full_unstemmed | Lymphocyte antigen 6 complex locus G6D downregulation is a novel parameter for functional impairment of neutrophils in aged mice |
title_short | Lymphocyte antigen 6 complex locus G6D downregulation is a novel parameter for functional impairment of neutrophils in aged mice |
title_sort | lymphocyte antigen 6 complex locus g6d downregulation is a novel parameter for functional impairment of neutrophils in aged mice |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647080/ https://www.ncbi.nlm.nih.gov/pubmed/36389807 http://dx.doi.org/10.3389/fimmu.2022.1001179 |
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