4.5 Article

Short-Term Environmental Enrichment is a Stronger Modulator of Brain Glial Cells and Cervical Lymph Node T Cell Subtypes than Exercise or Combined Exercise and Enrichment

Journal

CELLULAR AND MOLECULAR NEUROBIOLOGY
Volume 41, Issue 3, Pages 469-486

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10571-020-00862-x

Keywords

Environmental enrichment; Physical exercise; Aging; Microglia; Astrocytes; T cells

Funding

  1. Projekt DEAL
  2. National Health and Medical Research Council Australia [APP 1043771]
  3. National Health and Medical Research Council (NHMRC)

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In the short-term, environmental enrichment (EE) has a stronger modulatory effect on microglial and peripheral T cell subset numbers in mice compared to physical exercise (PE) and PE + EE, which shows no additive effects.
Physical exercise (PE) and environmental enrichment (EE) can modulate immunity. However, the differential effects of short-term PE, EE, and PE + EE on neuroimmune mechanisms during normal aging has not been elucidated. Hence, a cohort of 3-, 8-, and 13-month-old immunologically unchallenged C57BL/6 wild-type mice were randomly assigned to either Control, PE, EE, or PE + EE groups and provided with either no treatment, a running wheel, a variety of plastic and wooden objects alone or in combination with a running wheel for seven weeks, respectively. Immunohistochemistry and 8-color flow cytometry were used to determine the numbers of dentate gyrus glial cells, and the proportions of CD4(+) and CD8(+) T cell numbers and their subsets from cervical lymph nodes, respectively. An increase in the number of IBA1(+) microglia in the dentate gyrus at 5 and 10 months was observed after EE, while PE and PE + EE increased it only at 10 months. No change in astroglia number in comparison to controls were observed in any of the treatment groups. Also, all treatments induced significant differences in the proportion of specific T cell subsets, i.e., CD4(+) and CD8(+) T naive (T-N), central memory (T-CM), and effector memory (T-EM) cells. Our results suggest that in the short-term, EE is a stronger modulator of microglial and peripheral T cell subset numbers than PE and PE + EE, and the combination of short-term PE and EE has no additive effects.

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