Hypoxia induces senescence of bone marrow mesenchymal stem cells via altered gut microbiota

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作者
Junyue Xing
Yongquan Ying
Chenxi Mao
Yiwei Liu
Tingting Wang
Qian Zhao
Xiaoling Zhang
Fuxia Yan
Hao Zhang
机构
[1] Chinese Academy of Medical Sciences and Peking Union Medical College,State Key Laboratory of Cardiovascular Diseases, Fuwai Hospital, National Center for Cardiovascular Diseases
[2] Fuwai Hospital,Key Laboratory of Cardiac Regenerative Medicine, National Healthy Commission
[3] CAMS&PUMC,Center for Pediatric Cardiac Surgery, Fuwai Hospital
[4] Taizhou Hospital,Department of Thoracic and Cardiovascular Surgery
[5] 1st Affiliated Hospital of Wenzhou Medical University,Department of Thoracic and Cardiovascular Surgery
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Systemic chronic hypoxia is a feature of many diseases and may influence the communication between bone marrow (BM) and gut microbiota. Here we analyse patients with cyanotic congenital heart disease (CCHD) who are experiencing chronic hypoxia and characterize the association between bone marrow mesenchymal stem cells (BMSCs) and gut microbiome under systemic hypoxia. We observe premature senescence of BMSCs and abnormal d-galactose accumulation in patients with CCHD. The hypoxia that these patients experience results in an altered diversity of gut microbial communities, with a remarkable decrease in the number of Lactobacilli and a noticeable reduction in the amount of enzyme-degraded d-galactose. Replenishing chronic hypoxic rats with Lactobacillus reduced the accumulation of d-galactose and restored the deficient BMSCs. Together, our findings show that chronic hypoxia predisposes BMSCs to premature senescence, which may be due to gut dysbiosis and thus induced d-galactose accumulation.
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