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Gut microbiota of the young ameliorates physical fitness of the aged in mice.
Kim, Kwang H; Chung, Yusook; Huh, Ji-Won; Park, Dong Jin; Cho, Yejin; Oh, Yeseul; Jeong, Haengdueng; Yoon, Jaekyung; Kang, Ju-Hee; Shin, Hae-Sol; Kim, Hyoung-Chin; Kwon, Soon-Kyeong; Seo, Kyoung Yul; Oh, Seung Hyun; Seong, Je Kyung; Ha, Sang-Jun; Nam, Ki Taek; Kim, Jihyun F.
Afiliação
  • Kim KH; Severance Biomedical Science Institute, Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.
  • Chung Y; Department of Systems Biology, Division of Life Sciences, and Institute for Life Science and Biotechnology, Yonsei University, Seoul, Korea.
  • Huh JW; Department of Systems Biology, Division of Life Sciences, and Institute for Life Science and Biotechnology, Yonsei University, Seoul, Korea.
  • Park DJ; Department of Biochemistry and Division of Life Sciences, Yonsei University, Seoul, Korea.
  • Cho Y; Severance Biomedical Science Institute, Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.
  • Oh Y; Severance Biomedical Science Institute, Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.
  • Jeong H; Severance Biomedical Science Institute, Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.
  • Yoon J; Department of Systems Biology, Division of Life Sciences, and Institute for Life Science and Biotechnology, Yonsei University, Seoul, Korea.
  • Kang JH; College of Pharmacy, Gachon University, Incheon, Korea.
  • Shin HS; Korea Mouse Sensory Phenotyping Center (KMSPC), Yonsei University College of Medicine, Seoul, Korea.
  • Kim HC; Laboratory Animal Resource Center, Division of Bioinfrastructure, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Korea.
  • Kwon SK; Department of Systems Biology, Division of Life Sciences, and Institute for Life Science and Biotechnology, Yonsei University, Seoul, Korea.
  • Seo KY; Division of Applied Life Science (Brain Korea 21), Gyeongsang National University, Jinju, Korea.
  • Oh SH; Korea Mouse Sensory Phenotyping Center (KMSPC), Yonsei University College of Medicine, Seoul, Korea.
  • Seong JK; College of Pharmacy, Gachon University, Incheon, Korea.
  • Ha SJ; Korea Mouse Phenotyping Center (KMPC), Seoul National University, Seoul, Korea.
  • Nam KT; Department of Biochemistry and Division of Life Sciences, Yonsei University, Seoul, Korea.
  • Kim JF; Severance Biomedical Science Institute, Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea. kitaek@yuhs.ac.
Microbiome ; 10(1): 238, 2022 12 26.
Article em En | MEDLINE | ID: mdl-36567320
ABSTRACT

BACKGROUND:

Aging is a natural process that an organism gradually loses its physical fitness and functionality. Great efforts have been made to understand and intervene in this deteriorating process. The gut microbiota affects host physiology, and dysbiosis of the microbial community often underlies the pathogenesis of host disorders. The commensal microbiota also changes with aging; however, the interplay between the microbiota and host aging remains largely unexplored. Here, we systematically examined the ameliorating effects of the gut microbiota derived from the young on the physiology and phenotypes of the aged.

RESULTS:

As the fecal microbiota was transplanted from young mice at 5 weeks after birth into 12-month-old ones, the thickness of the muscle fiber and grip strength were increased, and the water retention ability of the skin was enhanced with thickened stratum corneum. Muscle thickness was also marginally increased in 25-month-old mice after transferring the gut microbiota from the young. Bacteria enriched in 12-month-old mice that received the young-derived microbiota significantly correlated with the improved host fitness and altered gene expression. In the dermis of these mice, transcription of Dbn1 was most upregulated and DBN1-expressing cells increased twice. Dbn1-heterozygous mice exhibited impaired skin barrier function and hydration.

CONCLUSIONS:

We revealed that the young-derived gut microbiota rejuvenates the physical fitness of the aged by altering the microbial composition of the gut and gene expression in muscle and skin. Dbn1, for the first time, was found to be induced by the young microbiota and to modulate skin hydration. Our results provide solid evidence that the gut microbiota from the young improves the vitality of the aged. Video Abstract.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microbiota / Microbioma Gastrointestinal Limite: Animals Idioma: En Revista: Microbiome Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microbiota / Microbioma Gastrointestinal Limite: Animals Idioma: En Revista: Microbiome Ano de publicação: 2022 Tipo de documento: Article