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Microbial Stimulation Reverses the Age-Related Decline in M Cells in Aged Mice.

ABSTRACT: Aging has a profound effect on the immune system, termed immunosenescence, resulting in increased incidence and severity of infections and decreased efficacy of vaccinations. We previously showed that immunosurveillance in the intestine, achieved primarily through antigen sampling M cells in the follicle associated epithelium (FAE) of Peyer's patches, was compromised during aging due to a decline in M cell functional maturation. The intestinal microbiota also changes significantly with age, but whether this affects M cell maturation was not known. We show that housing of aged mice on used bedding from young mice, or treatment with bacterial flagellin, were each sufficient to enhance the functional maturation of M cells in Peyer's patches. An understanding of the mechanisms underlying the influence of the intestinal microbiota on M cells has the potential to lead to new methods to enhance the efficacy of oral vaccination in aged individuals.

SUBMITTER: Donaldson DS

PROVIDER: S-EPMC7251786 | biostudies-literature | 2020 Jun

REPOSITORIES: biostudies-literature

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Microbial Stimulation Reverses the Age-Related Decline in M Cells in Aged Mice.

Donaldson David S DS Pollock Jolinda J Vohra Prerna P Stevens Mark P MP Mabbott Neil A NA

iScience 20200511 6

Aging has a profound effect on the immune system, termed immunosenescence, resulting in increased incidence and severity of infections and decreased efficacy of vaccinations. We previously showed that immunosurveillance in the intestine, achieved primarily through antigen sampling M cells in the follicle associated epithelium (FAE) of Peyer's patches, was compromised during aging due to a decline in M cell functional maturation. The intestinal microbiota also changes significantly with age, but ...[more]

PMID: 32454449

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Dataset Information

Microbial Stimulation Reverses the Age-Related Decline in M Cells in Aged Mice.

Publications

Microbial Stimulation Reverses the Age-Related Decline in M Cells in Aged Mice.

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