Cited by 322T-cell and B-cell ImmunologyHematopoietic Stem Cell TransplantationImmunotoxicology and immune responses

Thymic output in aged mice

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Hale, J. Scott, Boursalian, Tamar E., Turk, Gail L., Fink, Pamela J.·2006·Proceedings of the National Academy of Sciences

Abstract

Using GFP to mark recent thymic emigrants (RTEs) in mice carrying a GFP transgene driven by the recombination-activating gene 2 promoter, we demonstrate that RTEs are readily detectable even in 2-year-old mice, despite the fact that the proportion of the peripheral T cell pool comprised of RTEs declines with age. Although the number of RTEs decreases after reaching a peak at 6 weeks of age, thymic output as a function of thymic size is surprisingly age-independent. The CD4:CD8 ratio of RTEs declines with age, partly because of a striking decrease in steady-state proliferation of CD4 + RTEs in older mice. RTEs in aged mice undergo phenotypic maturation in the lymphoid periphery with delayed kinetics compared with young mice. RTEs from aged mice secrete less IL-2, proliferate less well, and achieve only weak expression of early-activation markers compared with more mature naïve peripheral T cells from the same mice. The proportion of GFP − cells in the CD4 + and CD8 + thymic compartments increases with age, partly as a result of leakiness in the aged thymus, allowing reentry of naïve peripheral T cells.

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  • Thymic involution contributes to age-dependent loss of T cell immunity in mice.

    “Thymic involution clearly contributes to the aging-dependent loss of T cell immunity in mice”

    From Successful and Maladaptive T Cell Aging (2017) · cites this paper as Hale et al., 2006

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  1. Berzins, S. P., Godfrey, D. I., Miller, J. F. A. P. & Boyd, R. L. (1999) Proc. Natl. Acad. Sci. USA 96, 9787-9791.
  2. Kong, F. K., Chen, C. L., Six, A., Hockett, R. D. & Cooper, M. D. (1999) Proc. Natl. Acad. Sci. USA 96, 1536-1540.

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Authors
Hale, J. S., Boursalian, T. E., Turk, G. L., & Fink, P. J.
Affiliations
University of Washington (US)
Corresponding author
Fink, Pamela J.
Venue
Proceedings of the National Academy of Sciences
Published
2006-05-30
Volume
103
Issue
22
Pages
8447-8452
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2156646599
Cited by
322
References
34
Citations by year
2026: 14 · 2025: 21 · 2024: 13 · 2023: 21 · 2022: 12 · 2021: 18 · 2020: 22 · 2019: 16 · 2018: 16 · 2017: 16 · 2016: 11 · 2015: 16 · 2014: 14 · 2013: 18 · 2012: 18
FWCI
5.90
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Cancer Research Institute
  • National Institutes of Health (AI064318)
  • National Institute on Aging (R21AG023781)
  • National Institute of Allergy and Infectious Diseases (R01AI064318)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotoxicology and immune responses
Keywords
thymic output, thymic emigrants, aging, recent thymic emigrants, CD4/CD8 ratio, T cell proliferation, T cell development, IL-2 secretion, thymus, aged mice
MeSH terms
Aging, Animals, Cell Movement, Cells, Cultured, Immunity, Innate, Kinetics, Organ Size, Phenotype, Thymus Gland, CD4-Positive T-Lymphocytes, CD8-Positive T-Lymphocytes, Lymphocyte Count, Cell Proliferation, Mice

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