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Alterations induced by chronic stress in lymphocyte subsets of blood and primary and secondary immune organs of mice

BACKGROUND: The immune system is particularly sensitive to stress. Although acute stress generally has positive effects, chronic stress typically provokes immunosuppression. The elucidation of the mechanisms involved in immunosuppression are of interest for the design of therapeutic approaches to av...

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Autores principales: Domínguez-Gerpe, Lourdes, Rey-Méndez, Manuel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC37547/
https://www.ncbi.nlm.nih.gov/pubmed/11518541
http://dx.doi.org/10.1186/1471-2172-2-7
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author Domínguez-Gerpe, Lourdes
Rey-Méndez, Manuel
author_facet Domínguez-Gerpe, Lourdes
Rey-Méndez, Manuel
author_sort Domínguez-Gerpe, Lourdes
collection PubMed
description BACKGROUND: The immune system is particularly sensitive to stress. Although acute stress generally has positive effects, chronic stress typically provokes immunosuppression. The elucidation of the mechanisms involved in immunosuppression are of interest for the design of therapeutic approaches to avoid the appearance of stress disorders. This study aimed to investigate chronic stress-induced alterations on lymphocyte subset distribution and percentages. The experiments were performed with C57BL/6 mice subjected to chronic immobilization stress. RESULTS: Stress caused a marked increase in apoptosis inside the thymus, and a reduction in the total number of thymocytes. Furthermore, the proportion of immature thymocytes declined significantly suggesting that the increased apoptosis mainly affected cells of immature phenotype. In blood, the total number of lymphocytes diminished but not all lymphocyte populations showed the same tendency: while the relative proportion of B cells declined slightly, the relative proportion of circulating CD3(+) cells, and particularly some T cell subsets showing an immature phenotype (CD3(+)PNA(+)), increased under stress. The spleen and lymph nodes show a marked reduction in cellularity, but the relative proportion of T cells increased, while no change or only a slight reduction was observed in the relative proportion of B cells. Similarly, the relative proportion of T cells increased in bone marrow. CONCLUSIONS: Detailed data on the alterations of lymphoid cell subsets occurring under immobilization stress, both in the bloodstream and in different lymphoid tissues, are obtained. In general, T cells are more affected than B cells and, in particular, a marked increase in the percentage of a subset of circulating PNA(+)CD3(+) T cells is observed.
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spelling pubmed-375472001-08-24 Alterations induced by chronic stress in lymphocyte subsets of blood and primary and secondary immune organs of mice Domínguez-Gerpe, Lourdes Rey-Méndez, Manuel BMC Immunol Research Article BACKGROUND: The immune system is particularly sensitive to stress. Although acute stress generally has positive effects, chronic stress typically provokes immunosuppression. The elucidation of the mechanisms involved in immunosuppression are of interest for the design of therapeutic approaches to avoid the appearance of stress disorders. This study aimed to investigate chronic stress-induced alterations on lymphocyte subset distribution and percentages. The experiments were performed with C57BL/6 mice subjected to chronic immobilization stress. RESULTS: Stress caused a marked increase in apoptosis inside the thymus, and a reduction in the total number of thymocytes. Furthermore, the proportion of immature thymocytes declined significantly suggesting that the increased apoptosis mainly affected cells of immature phenotype. In blood, the total number of lymphocytes diminished but not all lymphocyte populations showed the same tendency: while the relative proportion of B cells declined slightly, the relative proportion of circulating CD3(+) cells, and particularly some T cell subsets showing an immature phenotype (CD3(+)PNA(+)), increased under stress. The spleen and lymph nodes show a marked reduction in cellularity, but the relative proportion of T cells increased, while no change or only a slight reduction was observed in the relative proportion of B cells. Similarly, the relative proportion of T cells increased in bone marrow. CONCLUSIONS: Detailed data on the alterations of lymphoid cell subsets occurring under immobilization stress, both in the bloodstream and in different lymphoid tissues, are obtained. In general, T cells are more affected than B cells and, in particular, a marked increase in the percentage of a subset of circulating PNA(+)CD3(+) T cells is observed. BioMed Central 2001-07-31 /pmc/articles/PMC37547/ /pubmed/11518541 http://dx.doi.org/10.1186/1471-2172-2-7 Text en Copyright © 2001 Domínguez-Gerpe and Rey-Méndez; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Domínguez-Gerpe, Lourdes
Rey-Méndez, Manuel
Alterations induced by chronic stress in lymphocyte subsets of blood and primary and secondary immune organs of mice
title Alterations induced by chronic stress in lymphocyte subsets of blood and primary and secondary immune organs of mice
title_full Alterations induced by chronic stress in lymphocyte subsets of blood and primary and secondary immune organs of mice
title_fullStr Alterations induced by chronic stress in lymphocyte subsets of blood and primary and secondary immune organs of mice
title_full_unstemmed Alterations induced by chronic stress in lymphocyte subsets of blood and primary and secondary immune organs of mice
title_short Alterations induced by chronic stress in lymphocyte subsets of blood and primary and secondary immune organs of mice
title_sort alterations induced by chronic stress in lymphocyte subsets of blood and primary and secondary immune organs of mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC37547/
https://www.ncbi.nlm.nih.gov/pubmed/11518541
http://dx.doi.org/10.1186/1471-2172-2-7
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