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B and T Lymphocyte Densities Remain Stable With Age in Human Cortex

One hallmark of human aging is increased brain inflammation represented by glial activation. With age, there is also diminished function of the adaptive immune system, and modest decreases in circulating B- and T-lymphocytes. Lymphocytes traffic through the human brain and reside there in small numb...

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Autores principales: Berry, Kacey, Farias-Itao, Daniela S., Grinberg, Lea T., Plowey, Edward D., Schneider, Julie A., Rodriguez, Roberta D., Suemoto, Claudia K., Buckwalter, Marion S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168031/
https://www.ncbi.nlm.nih.gov/pubmed/34056948
http://dx.doi.org/10.1177/17590914211018117
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author Berry, Kacey
Farias-Itao, Daniela S.
Grinberg, Lea T.
Plowey, Edward D.
Schneider, Julie A.
Rodriguez, Roberta D.
Suemoto, Claudia K.
Buckwalter, Marion S.
author_facet Berry, Kacey
Farias-Itao, Daniela S.
Grinberg, Lea T.
Plowey, Edward D.
Schneider, Julie A.
Rodriguez, Roberta D.
Suemoto, Claudia K.
Buckwalter, Marion S.
author_sort Berry, Kacey
collection PubMed
description One hallmark of human aging is increased brain inflammation represented by glial activation. With age, there is also diminished function of the adaptive immune system, and modest decreases in circulating B- and T-lymphocytes. Lymphocytes traffic through the human brain and reside there in small numbers, but it is unknown how this changes with age. Thus we investigated whether B- and T-lymphocyte numbers change with age in the normal human brain. We examined 16 human subjects in a pilot study and then 40 human subjects from a single brain bank, ranging in age from 44–96 years old, using rigorous criteria for defining neuropathological changes due to age alone. We immunostained post-mortem cortical tissue for B- and T-lymphocytes using antibodies to CD20 and CD3, respectively. We quantified cell density and made a qualitative assessment of cell location in cortical brain sections, and reviewed prior studies. We report that density and location of both B- and T-lymphocytes do not change with age in the normal human cortex. Solitary B-lymphocytes were found equally in intravascular, perivascular, and parenchymal locations, while T-lymphocytes appeared primarily in perivascular clusters. Thus, any change in number or location of lymphocytes in an aging brain may indicate disease rather than normal aging.
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spelling pubmed-81680312021-06-07 B and T Lymphocyte Densities Remain Stable With Age in Human Cortex Berry, Kacey Farias-Itao, Daniela S. Grinberg, Lea T. Plowey, Edward D. Schneider, Julie A. Rodriguez, Roberta D. Suemoto, Claudia K. Buckwalter, Marion S. ASN Neuro Original Paper One hallmark of human aging is increased brain inflammation represented by glial activation. With age, there is also diminished function of the adaptive immune system, and modest decreases in circulating B- and T-lymphocytes. Lymphocytes traffic through the human brain and reside there in small numbers, but it is unknown how this changes with age. Thus we investigated whether B- and T-lymphocyte numbers change with age in the normal human brain. We examined 16 human subjects in a pilot study and then 40 human subjects from a single brain bank, ranging in age from 44–96 years old, using rigorous criteria for defining neuropathological changes due to age alone. We immunostained post-mortem cortical tissue for B- and T-lymphocytes using antibodies to CD20 and CD3, respectively. We quantified cell density and made a qualitative assessment of cell location in cortical brain sections, and reviewed prior studies. We report that density and location of both B- and T-lymphocytes do not change with age in the normal human cortex. Solitary B-lymphocytes were found equally in intravascular, perivascular, and parenchymal locations, while T-lymphocytes appeared primarily in perivascular clusters. Thus, any change in number or location of lymphocytes in an aging brain may indicate disease rather than normal aging. SAGE Publications 2021-05-30 /pmc/articles/PMC8168031/ /pubmed/34056948 http://dx.doi.org/10.1177/17590914211018117 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Paper
Berry, Kacey
Farias-Itao, Daniela S.
Grinberg, Lea T.
Plowey, Edward D.
Schneider, Julie A.
Rodriguez, Roberta D.
Suemoto, Claudia K.
Buckwalter, Marion S.
B and T Lymphocyte Densities Remain Stable With Age in Human Cortex
title B and T Lymphocyte Densities Remain Stable With Age in Human Cortex
title_full B and T Lymphocyte Densities Remain Stable With Age in Human Cortex
title_fullStr B and T Lymphocyte Densities Remain Stable With Age in Human Cortex
title_full_unstemmed B and T Lymphocyte Densities Remain Stable With Age in Human Cortex
title_short B and T Lymphocyte Densities Remain Stable With Age in Human Cortex
title_sort b and t lymphocyte densities remain stable with age in human cortex
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168031/
https://www.ncbi.nlm.nih.gov/pubmed/34056948
http://dx.doi.org/10.1177/17590914211018117
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