Male rat leukocyte population dynamics predict a window for intervention in aging

Author:

Yanai Hagai1ORCID,Dunn Christopher2ORCID,Park Bongsoo1,Coletta Christopher3,McDevitt Ross A4ORCID,McNeely Taylor1,Leone Michael1,Wersto Robert P2,Perdue Kathy A4,Beerman Isabel1ORCID

Affiliation:

1. Epigenetics and Stem Cell Unit, Translational Gerontology Branch, National Institute on Aging

2. Flow Cytometry Core, National Institute on Aging

3. Computational Biology and Genomics Core, Laboratory of Genetics & Genomics, National Institute on Aging

4. Comparative Medicine Section, National Institute on Aging

Abstract

Many age-associated changes in the human hematopoietic system have been reproduced in murine models; however, such changes have not been as robustly explored in rats despite the fact these larger rodents are more physiologically similar to humans. We examined peripheral blood of male F344 rats ranging from 3 to 27 months of age and found significant age-associated changes with distinct leukocyte population shifts. We report CD25+ CD4+ population frequency is a strong predictor of healthy aging, generate a model using blood parameters, and find rats with blood profiles that diverge from chronologic age indicate debility; thus, assessments of blood composition may be useful for non-lethal disease profiling or as a surrogate measure for efficacy of aging interventions. Importantly, blood parameters and DNA methylation alterations, defined distinct juncture points during aging, supporting a non-linear aging process. Our results suggest these inflection points are important considerations for aging interventions. Overall, we present rat blood aging metrics that can serve as a resource to evaluate health and the effects of interventions in a model system physiologically more reflective of humans.

Funder

National Institutes of Health

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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