Developmental interactions of CD4 T cells and thymocytes: age-related differential effects

Masha Fridkis-Hareli, Ramit Mehr, Loya Abel, Amiela Globerson

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

The study was designed to determine whether the developmental potential of immature thymocytes in the thymus is altered in aging, and whether concomitantly present mature T cells have any feedback effect. The strategy was to seed sorted double negative, CD4-CD8-(DN) thymocytes on their own, or in the presence of mature T cells, onto lymphoid depleted fetal thymus (FT) explants, and to examine the resulting T cell subsets. Thymocyte donors were young (2-3 months) and old (24 months) C57BL/6J, Thy1.2 mice and splenocytes were from C57BL/Ka, Thy1.1 mice. The DN cells of the old gave rise to lower values of double positive CD4+CD8+ (DP) cells than those of the young. Cocultures containing a mixture of DN thymocytes and CD4+CD8- splenocytes showed higher CD4+CD8- and DN, and lower DP and CD4-CD8+ levels in the old-donor derived cells, as compared with the young ones. Similar results were obtained with CD4+CD8- thymocytes. In contrast, the presence of CD4-CD8+ splenocytes had no effect on the pattern of DN cell development. Our data indicate that differentiation of CD4/CD8 thymocyte phenotypes is affected by CD4+ cells, in an age-associated differential manner.

Original languageEnglish
Pages (from-to)169-178
Number of pages10
JournalMechanisms of Ageing and Development
Volume73
Issue number3
DOIs
StatePublished - Mar 1994
Externally publishedYes

Bibliographical note

Funding Information:
Hana Stup is acknowledged. Supported by the Austrian National Bank (Project No. 3556). A.G. is the incumbent of the Harriet and Harold Brady Chair in Cancer Research.

Funding

Hana Stup is acknowledged. Supported by the Austrian National Bank (Project No. 3556). A.G. is the incumbent of the Harriet and Harold Brady Chair in Cancer Research.

FundersFunder number
Oesterreichische Nationalbank3556

    Keywords

    • Aging
    • T lymphocytes
    • Thymic microenvironment

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