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Ectopic cervical thymi and no thymic involution until midlife in naked mole rats
Immunosenescence is a hallmark of aging and manifests as increased susceptibility to infection, autoimmunity, and cancer in the elderly. One component of immunosenescence is thymic involution, age‐associated shrinkage of the thymus, observed in all vertebrates studied to date. The naked mole rat (He...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520710/ https://www.ncbi.nlm.nih.gov/pubmed/34596321 http://dx.doi.org/10.1111/acel.13477 |
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author | Emmrich, Stephan Tolibzoda Zakusilo, Frances Trapp, Alexandre Zhou, Xuming Zhang, Quanwei Irving, Ellen M. Drage, Michael G. Zhang, Zhengdong Gladyshev, Vadim N. Seluanov, Andrei Gorbunova, Vera |
author_facet | Emmrich, Stephan Tolibzoda Zakusilo, Frances Trapp, Alexandre Zhou, Xuming Zhang, Quanwei Irving, Ellen M. Drage, Michael G. Zhang, Zhengdong Gladyshev, Vadim N. Seluanov, Andrei Gorbunova, Vera |
author_sort | Emmrich, Stephan |
collection | PubMed |
description | Immunosenescence is a hallmark of aging and manifests as increased susceptibility to infection, autoimmunity, and cancer in the elderly. One component of immunosenescence is thymic involution, age‐associated shrinkage of the thymus, observed in all vertebrates studied to date. The naked mole rat (Heterocephalus glaber) has become an attractive animal model in aging research due to its extreme longevity and resistance to disease. Here, we show that naked mole rats display no thymic involution up to 11 years of age. Furthermore, we found large ectopic cervical thymi in addition to the canonical thoracic thymus, both being identical in their cell composition. The developmental landscape in naked mole rat thymi revealed overt differences from the murine T‐cell compartment, most notably a decrease of CD4(+)/CD8(+) double‐positive cells and lower abundance of cytotoxic effector T cells. Our observations suggest that naked mole rats display a delayed immunosenescence. Therapeutic interventions aimed at reversing thymic aging remain limited, underscoring the importance of understanding the cellular and molecular mechanisms behind a sustained immune function in the naked mole rat. |
format | Online Article Text |
id | pubmed-8520710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85207102021-10-25 Ectopic cervical thymi and no thymic involution until midlife in naked mole rats Emmrich, Stephan Tolibzoda Zakusilo, Frances Trapp, Alexandre Zhou, Xuming Zhang, Quanwei Irving, Ellen M. Drage, Michael G. Zhang, Zhengdong Gladyshev, Vadim N. Seluanov, Andrei Gorbunova, Vera Aging Cell Original Papers Immunosenescence is a hallmark of aging and manifests as increased susceptibility to infection, autoimmunity, and cancer in the elderly. One component of immunosenescence is thymic involution, age‐associated shrinkage of the thymus, observed in all vertebrates studied to date. The naked mole rat (Heterocephalus glaber) has become an attractive animal model in aging research due to its extreme longevity and resistance to disease. Here, we show that naked mole rats display no thymic involution up to 11 years of age. Furthermore, we found large ectopic cervical thymi in addition to the canonical thoracic thymus, both being identical in their cell composition. The developmental landscape in naked mole rat thymi revealed overt differences from the murine T‐cell compartment, most notably a decrease of CD4(+)/CD8(+) double‐positive cells and lower abundance of cytotoxic effector T cells. Our observations suggest that naked mole rats display a delayed immunosenescence. Therapeutic interventions aimed at reversing thymic aging remain limited, underscoring the importance of understanding the cellular and molecular mechanisms behind a sustained immune function in the naked mole rat. John Wiley and Sons Inc. 2021-10-01 2021-10 /pmc/articles/PMC8520710/ /pubmed/34596321 http://dx.doi.org/10.1111/acel.13477 Text en © 2021 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Emmrich, Stephan Tolibzoda Zakusilo, Frances Trapp, Alexandre Zhou, Xuming Zhang, Quanwei Irving, Ellen M. Drage, Michael G. Zhang, Zhengdong Gladyshev, Vadim N. Seluanov, Andrei Gorbunova, Vera Ectopic cervical thymi and no thymic involution until midlife in naked mole rats |
title | Ectopic cervical thymi and no thymic involution until midlife in naked mole rats |
title_full | Ectopic cervical thymi and no thymic involution until midlife in naked mole rats |
title_fullStr | Ectopic cervical thymi and no thymic involution until midlife in naked mole rats |
title_full_unstemmed | Ectopic cervical thymi and no thymic involution until midlife in naked mole rats |
title_short | Ectopic cervical thymi and no thymic involution until midlife in naked mole rats |
title_sort | ectopic cervical thymi and no thymic involution until midlife in naked mole rats |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520710/ https://www.ncbi.nlm.nih.gov/pubmed/34596321 http://dx.doi.org/10.1111/acel.13477 |
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