| Literature DB >> 33815871 |
Huijuan Shu1,2,3, Zhongxin Guo1,2,3, Xiangren Chen1,2,3, Shuya Qi1,2, Xinxin Xiong1,2, Shuang Xia1,2,3, Qingyun Huang1,2, Ling Lan1,2, Jiangu Gong1,2, Shaoming Huang1,2, Boning Yang1,2, Guohe Tan1,2,3.
Abstract
Manganese (Mn) is a potent neurotoxin known to cause long-lasting structural damage and progressive cognitive deficits in the brain. However, new therapeutic approaches are urgently needed since current treatments only target symptoms of Mn exposure. Recent studies have suggested a potential role for multipotent neural stem cells (NSCs) in the etiology of Mn-induced cognitive deficits. In this study, we evaluated the effect of direct intracerebral transplantation of NSCs on cognitive function of mice chronically exposed to MnCl2, and further explored the distribution of transplanted NSCs in brain tissues. NSCs were isolated and bilaterally injected into the hippocampal regions or lateral ventricles of Mn-exposed mice. The results showed that many transplanted cells migrated far away from the injection sites and survived in vivo in the Mn-exposed mouse brain, implying enhanced neurogenesis in the host brain. We found that NSCs transplanted into either the hippocampal regions or the lateral ventricles significantly improved spatial learning and memory function of the Mn-exposed mice in the Morris water maze. Immunofluorescence analyses indicated that some surviving NSCs differentiated into neurons or glial cells, which may have become functionally integrated into the impaired local circuits, providing a possible cellular basis for the improvement of cognitive function in NSC-transplanted mice. Taken together, our findings confirm the Mn-induced impairment of neurogenesis in the brain and underscore the potential of treating Mn exposure by NSC transplantation, providing a practical therapeutic strategy against this type of neurotoxicity. copyright:Entities:
Keywords: cell transplantation; learning and memory; manganese neurotoxicity; neural stem cells
Year: 2021 PMID: 33815871 PMCID: PMC7990353 DOI: 10.14336/AD.2020.0717
Source DB: PubMed Journal: Aging Dis ISSN: 2152-5250 Impact factor: 6.745