4.7 Article

Intracerebral Transplantation of Neural Stem Cells Restores Manganese-Induced Cognitive Deficits in Mice

Journal

AGING AND DISEASE
Volume 12, Issue 2, Pages 371-385

Publisher

INT SOC AGING & DISEASE
DOI: 10.14336/AD.2020.0717

Keywords

neural stem cells; cell transplantation; manganese neurotoxicity; learning and memory

Funding

  1. National Natural Science Foundation of China [81660548, 81571268, 81371431]
  2. Guangxi Natural Science Foundation Program [2015GXNSFGA139005, AD17195079, 2018GXNSFAA294107, 2018GXNSFAA 294109]
  3. Innovation Project of Guangxi Graduate Education [JGY2017039, YCSW2017113]
  4. Guangxi Medical University Training Program for Distinguished Young Scholars

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The study suggests that direct intracerebral transplantation of neural stem cells can improve cognitive function in mice exposed to manganese, possibly by enhancing neurogenesis in the host brain and providing a potential cellular basis for cognitive improvement. This research underscores the potential of treating manganese exposure through NSC transplantation.
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 MnCI2, 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.

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