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

机译:低氧通过改变肠道菌群诱导骨髓间充质干细胞衰老

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摘要

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.
机译:系统性慢性低氧是许多疾病的特征,可能影响骨髓(BM)与肠道菌群之间的通讯。在这里,我们分析了患有慢性低氧的紫cyan性先天性心脏病(CCHD)患者,并表征了系统性低氧下骨髓间充质干细胞(BMSC)与肠道微生物组之间的关联。我们观察到CCHD患者的BMSCs早衰和d-半乳糖异常蓄积。这些患者经历的缺氧导致肠道微生物群落多样性的改变,乳酸杆菌的数量显着减少,酶降解的d-半乳糖的数量明显减少。用乳酸杆菌补充慢性低氧大鼠减少了d-半乳糖的积累并恢复了缺乏的骨髓间充质干细胞。在一起,我们的研究结果表明,慢性低氧使BMSCs易于过早衰老,这可能是由于肠道营养不良所致,并因此诱导了d-半乳糖的积累。

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