Literature DB >> 18648098

Characterization of age- and gender-related changes in the spleen and thymus from control cynomolgus macaques used in toxicity studies.

Melanie S Spoor1, Zaher A Radi, Robert W Dunstan.   

Abstract

Age- and gender-related lymphoid tissue variability in control male and female monkeys of various ages (under three years; three to six years; seven to fifteen years) was characterized. Spleen and thymus organ weights, organ-to-body and organ-to-brain ratios, morphology by light microscopy, and B- and T-cell immunohistochemistry (IHC) were evaluated. Splenic weights and ratios were not significantly different between various age groups or genders, except males and females in the three-to-six-years age group, who exhibited statistically significant changes from the under-three-years age group. No differences in the number of primary follicles, secondary follicles with germinal centers, B-cell follicles, and periarterial lymphoid sheath were seen between age groups or genders, and no trends were noted in the spleen. By IHC, no differences were observed in B- and T-cell splenic densities. Several age- and gender-related changes in weights and ratios were noted in the thymus. The thymus had a trend toward increased interlobular fat infiltration with increasing age in both males and females. Thymic delineation of the cortex and medulla was significantly decreased in the seven-to-fifteen-years age group for males only. The cortex-to-medulla ratio was significantly lower only in males in the seven-to-fifteen-years age group. B- and T-cell cellular density did not change across various ages.

Entities:  

Mesh:

Year:  2008        PMID: 18648098     DOI: 10.1177/0192623308320279

Source DB:  PubMed          Journal:  Toxicol Pathol        ISSN: 0192-6233            Impact factor:   1.902


  5 in total

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Journal:  Dose Response       Date:  2018-09-25       Impact factor: 2.658

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Journal:  Int J Genomics       Date:  2019-04-21       Impact factor: 2.326

5.  Tumor-host signaling interaction reveals a systemic, age-dependent splenic immune influence on tumor development.

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  5 in total

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