Literature DB >> 19577818

Role of ovarian hormones in age-associated thymic involution revisited.

Milica Perisić1, Nevena Arsenović-Ranin, Ivan Pilipović, Dusko Kosec, Vesna Pesić, Katarina Radojević, Gordana Leposavić.   

Abstract

A commonly held view that ovarian hormones are causally involved in age-associated thymic involution has been recently challenged. In particular, their relevance in the progression of thymic involution has been disputed. To reassess this issue 10-month-old rats with well advanced thymic involutive changes were ovariectomized (Ovx), and after 1 month thymic cellularity, thymocyte development and levels of recent thymic emigrants (RTEs) were examined in peripheral blood and spleen. In addition, the distribution of major conventional and regulatory T-cell subsets was analyzed in the same peripheral lymphocyte compartments. Ovariectomy increased thymic weight and cellularity above the levels in both 10-month-old and age-matched controls indicating that ovarian hormone ablation not only prevented further progression of thymic involution, but also reversed it. The increased thymic cellularity was accompanied by altered thymocyte differentiation/maturation culminating in increased thymic output of naïve T cells as indicated by elevated levels of both CD4+ and CD8+ RTEs in peripheral blood and spleen. The changes in T-cell development produced: (i) a disproportional increase in cellularity across thymocyte subsets, so that relative proportions of cells at all maturational stages preceding the CD4+CD8+ T cell receptor (TCR)alphabeta(low) stage were reduced; the relative numbers of CD4+CD8+ TCRalphabeta(low) cells entering positive selection and their immediate CD4+CD8+ TCRalphabeta(high) descendents were increased, while those of the most mature CD4+CD8- and CD4-CD8+ TCRalphabeta(high) cells remained unaltered; (ii) enhanced cell proliferation across all thymocyte subsets and (iii) reduced apoptosis of cells within the CD4+CD8+ thymocyte subset. The augmented thymic output of naïve T cells in Ovx rats most likely reflected an early disinhibition of thymocyte development followed by increased positive/reduced negative selection, at least partly, due to raised thymocyte surface Thy-1 expression. The greater number of CD4+CD25+Foxp3+ cells in both thymus and peripheral blood suggested augmented thymic production of these cells. In addition, an increased CD4+/CD8+ cell ratio was found in the spleen of Ovx rats. Thus, ovarian hormone ablation led not only to increased diversity of the T-cell repertoire, but also to a new balance among distinct T-cell subsets in the periphery. 2009 Elsevier GmbH. All rights reserved.

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Year:  2009        PMID: 19577818     DOI: 10.1016/j.imbio.2009.06.012

Source DB:  PubMed          Journal:  Immunobiology        ISSN: 0171-2985            Impact factor:   3.144


  6 in total

Review 1.  Role of gonadal hormones in programming developmental changes in thymopoietic efficiency and sexual diergism in thymopoiesis.

Authors:  Gordana Leposavic; Milica Perisic; Ivan Pilipovic
Journal:  Immunol Res       Date:  2012-04       Impact factor: 2.829

2.  Accelerated immune senescence and reduced response to vaccination in ovariectomized female rhesus macaques.

Authors:  Flora Engelmann; Alex Barron; Henryk Urbanski; Martha Neuringer; Steven G Kohama; Byung Park; Ilhem Messaoudi
Journal:  Age (Dordr)       Date:  2010-09-03

Review 3.  The immune system and bone.

Authors:  Roberto Pacifici
Journal:  Arch Biochem Biophys       Date:  2010-06-17       Impact factor: 4.013

4.  Ovarian hormone level alterations during rat post-reproductive life-span influence CD8 + T-cell homeostasis.

Authors:  Nevena Arsenović-Ranin; Duško Kosec; Mirjana Nacka-Aleksić; Ivan Pilipović; Zorica Stojić-Vukanić; Jasmina Djikić; Biljana Bufan; Gordana Leposavić
Journal:  Exp Biol Med (Maywood)       Date:  2015-02-24

5.  Overexpression of Uromodulin-like1 accelerates follicle depletion and subsequent ovarian degeneration.

Authors:  W Wang; Y Tang; L Ni; E Kim; T Jongwutiwes; A Hourvitz; R Zhang; H Xiong; H-C Liu; Z Rosenwaks
Journal:  Cell Death Dis       Date:  2012-11-29       Impact factor: 8.469

6.  Elevated levels of interferon-γ production by memory T cells do not promote transplant tolerance resistance in aged recipients.

Authors:  James I Kim; Ryan T Stott; Julie Soohoo; Kang Mi Lee; Gaoping Zhao; Heidi Yeh; Shaoping Deng; James F Markmann
Journal:  PLoS One       Date:  2013-12-10       Impact factor: 3.240

  6 in total

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