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Lysosomes in T Cell Immunity and Aging
Lysosomes were initially recognized as degradation centers that regulate digestion and recycling of cellular waste. More recent studies document that the lysosome is an important signaling hub that regulates cell metabolism. Our knowledge of the role of lysosomes in immunity is mostly derived from i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9261317/ https://www.ncbi.nlm.nih.gov/pubmed/35822050 http://dx.doi.org/10.3389/fragi.2021.809539 |
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author | Jin, Jun Zhang, Huimin Weyand, Cornelia M. Goronzy, Jorg J. |
author_facet | Jin, Jun Zhang, Huimin Weyand, Cornelia M. Goronzy, Jorg J. |
author_sort | Jin, Jun |
collection | PubMed |
description | Lysosomes were initially recognized as degradation centers that regulate digestion and recycling of cellular waste. More recent studies document that the lysosome is an important signaling hub that regulates cell metabolism. Our knowledge of the role of lysosomes in immunity is mostly derived from innate immune cells, especially lysosomal degradation-specialized cells such as macrophages and dendritic cells. Their function in adaptive immunity is less understood. However, with the recent emphasis on metabolic regulation of T cell differentiation, lysosomes are entering center stage in T cell immunology. In this review, we will focus on the role of lysosomes in adaptive immunity and discuss recent findings on lysosomal regulation of T cell immune responses and lysosomal dysfunction in T cell aging. |
format | Online Article Text |
id | pubmed-9261317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92613172022-07-11 Lysosomes in T Cell Immunity and Aging Jin, Jun Zhang, Huimin Weyand, Cornelia M. Goronzy, Jorg J. Front Aging Aging Lysosomes were initially recognized as degradation centers that regulate digestion and recycling of cellular waste. More recent studies document that the lysosome is an important signaling hub that regulates cell metabolism. Our knowledge of the role of lysosomes in immunity is mostly derived from innate immune cells, especially lysosomal degradation-specialized cells such as macrophages and dendritic cells. Their function in adaptive immunity is less understood. However, with the recent emphasis on metabolic regulation of T cell differentiation, lysosomes are entering center stage in T cell immunology. In this review, we will focus on the role of lysosomes in adaptive immunity and discuss recent findings on lysosomal regulation of T cell immune responses and lysosomal dysfunction in T cell aging. Frontiers Media S.A. 2021-12-09 /pmc/articles/PMC9261317/ /pubmed/35822050 http://dx.doi.org/10.3389/fragi.2021.809539 Text en Copyright © 2021 Jin, Zhang, Weyand and Goronzy. 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 | Aging Jin, Jun Zhang, Huimin Weyand, Cornelia M. Goronzy, Jorg J. Lysosomes in T Cell Immunity and Aging |
title | Lysosomes in T Cell Immunity and Aging |
title_full | Lysosomes in T Cell Immunity and Aging |
title_fullStr | Lysosomes in T Cell Immunity and Aging |
title_full_unstemmed | Lysosomes in T Cell Immunity and Aging |
title_short | Lysosomes in T Cell Immunity and Aging |
title_sort | lysosomes in t cell immunity and aging |
topic | Aging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9261317/ https://www.ncbi.nlm.nih.gov/pubmed/35822050 http://dx.doi.org/10.3389/fragi.2021.809539 |
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