期刊
NANO RESEARCH
卷 -, 期 -, 页码 -出版社
TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-022-5032-9
关键词
gut microbiota-metabolism; melatonin; probiotics; nanoplastics exposure; hematopoietic injury
类别
资金
- National Natural Science Foundation of China [82073520, 81773397]
- Beijing Natural Science Program and Scientific Research Key Program of Beijing Municipal Commission of Education [KZ201810025032]
- Support Project of High-level Teachers in Beijing Municipal Universities in the Period of 13th Five-year Plan [CITTCD 20170323]
Plastic pollution is a significant global problem, and nanoplastics can cause hematotoxicity in bone marrow. This study investigated the biological distribution of nanoplastics in mouse bone marrow and their hematopoietic toxicity. The results showed that supplementation with probiotics and melatonin can ameliorate the hematopoietic damage caused by nanoplastics, with probiotics being more effective. Furthermore, the interventions with melatonin and probiotics may involve different microbes and metabolites, indicating potential mechanisms for regulating hematopoietic toxicity.
Plastic pollution has become a non-negligible global pollution problem. Nanoplastics (NP) can reach the bone marrow with blood circulation and develop hematotoxicity, but potential mechanisms and prevention strategies are lacking. Here, we report the biological distribution of NP particles in the bone marrow of mice and hematopoietic toxicity after exposure to 60 mu g of 80 nm NP for 42 days. NP exposure inhibited the capability of bone marrow hematopoietic stem cells to renew and differentiate. Notably, probiotics and melatonin supplementation significantly ameliorated NP-induced hematopoietic damage, and the former was superior to the latter. And interestingly, melatonin and probiotic interventions may involve different microbes and metabolites. After melatonin intervention, creatine showed a stronger correlation with NP-induced gut microbiota disorders. In contrast, probiotic intervention reversed the levels of more gut microbes and plasma metabolites. Of these, threonine, malonylcarnitine, and 3-hydroxybutyric acid might be potential performers in the regulation of hematopoietic toxicity by gut microbes, as they had a more significant relationship with the identified microbes. In conclusion, supplementation with melatonin or probiotics may be two candidates to prevent hematopoietic toxicity attributable to NP exposure. Also, the multi-omics results may lay the foundation for future investigations into in-depth mechanisms.
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