Microbiota from young mice counteracts selective age-associated behavioral deficits

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作者
Marcus Boehme
Katherine E. Guzzetta
Thomaz F. S. Bastiaanssen
Marcel van de Wouw
Gerard M. Moloney
Andreu Gual-Grau
Simon Spichak
Loreto Olavarría-Ramírez
Patrick Fitzgerald
Enrique Morillas
Nathaniel L. Ritz
Minal Jaggar
Caitlin S. M. Cowan
Fiona Crispie
Francisco Donoso
Evelyn Halitzki
Marta C. Neto
Marzia Sichetti
Anna V. Golubeva
Rachel S. Fitzgerald
Marcus J. Claesson
Paul D. Cotter
Olivia F. O’Leary
Timothy G. Dinan
John F. Cryan
机构
[1] APC Microbiome Ireland,Department of Anatomy and Neuroscience
[2] University College Cork,Department of Psychiatry and Neurobehavioural Science
[3] University College Cork,School of Microbiology
[4] Teagasc Food Research Centre,undefined
[5] Moorepark,undefined
[6] Fermoy,undefined
[7] University College Cork,undefined
[8] University College Cork,undefined
来源
Nature Aging | 2021年 / 1卷
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摘要
The gut microbiota is increasingly recognized as an important regulator of host immunity and brain health. The aging process yields dramatic alterations in the microbiota, which is linked to poorer health and frailty in elderly populations. However, there is limited evidence for a mechanistic role of the gut microbiota in brain health and neuroimmunity during aging processes. Therefore, we conducted fecal microbiota transplantation from either young (3–4 months) or old (19–20 months) donor mice into aged recipient mice (19–20 months). Transplant of a microbiota from young donors reversed aging-associated differences in peripheral and brain immunity, as well as the hippocampal metabolome and transcriptome of aging recipient mice. Finally, the young donor-derived microbiota attenuated selective age-associated impairments in cognitive behavior when transplanted into an aged host. Our results reveal that the microbiome may be a suitable therapeutic target to promote healthy aging.
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页码:666 / 676
页数:10
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