Age‐associated increase in the expression of T cell antigen receptor γ chain genes in mice

Goro Matsuzaki, Yasunobu Yoshikai, Kenji Kishihara, Koji Nomoto, Teruo Yokokura, Kikuo Nomoto

    Research output: Contribution to journalArticle

    11 Citations (Scopus)

    Abstract

    T cell function generally declines with age. To determine the underlying cause of the age‐related decline, we compared the expression levels of T cell antigen receptor genes encoding γ, β and α chains in the lymphoid tissues of young (8 wk old) vs. aged (40 wk old) mice. An age‐associated increase in γ chain gene transcripts was evident in the thymocytes, spleen cells and mesenteric lymph node cells. Aged mice had a relatively high proportion of CD3+CD4CD8 cells but a reduced level of CD3+CD4CD8+ cells in the lymphoid tissues, as compared with young counterparts. The allo‐reactivity in the lymphoid cells, as assessed by mixed lymphocyte reaction (MLR) responses, decreased with advancing age. On the contrary, increased levels of syngeneic MLR and spontaneous cytolytic activity were noted in the lymphoid cells of aged mice, as compared with findings in their young counterparts. A remarkable increase in the number of CD3+CD4CD8 cells and level of the γ chain gene messages was also detected in the responder cells of day 4 syngeneic MLR culture from aged mice. An increase in the number of T cells bearing γ chain may be related to the alterations in immunological functions in aged mice.

    Original languageEnglish
    Pages (from-to)1779-1784
    Number of pages6
    JournalEuropean Journal of Immunology
    Volume18
    Issue number11
    DOIs
    Publication statusPublished - Jan 1 1988

    All Science Journal Classification (ASJC) codes

    • Immunology and Allergy
    • Immunology

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  • Cite this

    Matsuzaki, G., Yoshikai, Y., Kishihara, K., Nomoto, K., Yokokura, T., & Nomoto, K. (1988). Age‐associated increase in the expression of T cell antigen receptor γ chain genes in mice. European Journal of Immunology, 18(11), 1779-1784. https://doi.org/10.1002/eji.1830181119