Microbiota-microglia connections in age-related cognition decline.


Journal

Aging cell
ISSN: 1474-9726
Titre abrégé: Aging Cell
Pays: England
ID NLM: 101130839

Informations de publication

Date de publication:
05 2022
Historique:
revised: 08 03 2022
received: 04 01 2022
accepted: 13 03 2022
pubmed: 30 3 2022
medline: 25 5 2022
entrez: 29 3 2022
Statut: ppublish

Résumé

Aging is an inevitable process that all individuals experience, of which the extent differs among individuals. It has been recognized as the risk factor of neurodegenerative diseases by affecting gut microbiota compositions, microglia, and cognition abilities. Aging-induced changes in gut microbiota compositions have a critical role in orchestrating the morphology and functions of microglia through the gut-brain axis. Gut microbiota communicates with microglia by its secreted metabolites and neurotransmitters. This is highly associated with age-related cognitive declines. Here, we review the main composition of microbiota in the aged individuals, outline the changes of the brain in age-related cognitive decline from a neuroinflammation perspective, especially the changes of morphology and functions of microglia, discuss the crosstalk between microbiota and microglia in the aged brain and further highlight the role of microbiota-microglia connections in neurodegenerative diseases (Alzheimer's disease and Parkinson's disease).

Identifiants

pubmed: 35349746
doi: 10.1111/acel.13599
pmc: PMC9124309
doi:

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13599

Informations de copyright

© 2022 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd.

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Auteurs

Rui Zhou (R)

Department of Nuclear Medicine and Medical PET Center, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong SAR, China.

Shufang Qian (S)

Department of Nuclear Medicine and Medical PET Center, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.

William C S Cho (WCS)

Department of Clinical Oncology, Queen Elizabeth Hospital, Hong Kong SAR, China.

Jinyun Zhou (J)

Department of Nuclear Medicine and Medical PET Center, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.

Chentao Jin (C)

Department of Nuclear Medicine and Medical PET Center, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.

Yan Zhong (Y)

Department of Nuclear Medicine and Medical PET Center, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.

Jing Wang (J)

Department of Nuclear Medicine and Medical PET Center, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.

Xiaohui Zhang (X)

Department of Nuclear Medicine and Medical PET Center, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.

Zhoujiao Xu (Z)

Department of Nuclear Medicine and Medical PET Center, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.

Mei Tian (M)

Department of Nuclear Medicine and Medical PET Center, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.

Lawrence W C Chan (LWC)

Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong SAR, China.

Hong Zhang (H)

Department of Nuclear Medicine and Medical PET Center, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Key Laboratory for Biomedical Engineering of Ministry of Education, Zhejiang University, Hangzhou, China.
The College of Biomedical Engineering and Instrument Science of Zhejiang University, Hangzhou, China.

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