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神经干细胞脑内移植可恢复锰诱导的小鼠认知缺陷。

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

作者信息

Shu Huijuan, Guo Zhongxin, Chen Xiangren, Qi Shuya, Xiong Xinxin, Xia Shuang, Huang Qingyun, Lan Ling, Gong Jiangu, Huang Shaoming, Yang Boning, Tan Guohe

机构信息

1Key Laboratory of Longevity and Aging-related Diseases of Chinese Ministry of Education, Guangxi Collaborative Innovation Center for Biomedicine & Guangxi Key Laboratory of Regenerative Medicine, Center for Translational Medicine, Guangxi Medical University, Nanning, Guangxi, China.

2Department of Human Anatomy, School of Basic Medical Sciences, Guangxi Medical University, Nanning, Guangxi, China.

出版信息

Aging Dis. 2021 Apr 1;12(2):371-385. doi: 10.14336/AD.2020.0717. eCollection 2021 Apr.

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 MnCl, 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 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.

摘要

锰(Mn)是一种强效神经毒素,已知会导致大脑长期的结构损伤和进行性认知缺陷。然而,由于目前的治疗仅针对锰暴露的症状,因此迫切需要新的治疗方法。最近的研究表明,多能神经干细胞(NSCs)在锰诱导的认知缺陷病因中可能发挥作用。在本研究中,我们评估了直接脑内移植神经干细胞对长期暴露于氯化锰的小鼠认知功能的影响,并进一步探讨了移植的神经干细胞在脑组织中的分布。分离神经干细胞并双侧注射到锰暴露小鼠的海马区域或侧脑室。结果表明,许多移植细胞从注射部位迁移到远处并在锰暴露的小鼠脑中存活,这意味着宿主脑中神经发生增强。我们发现,移植到海马区域或侧脑室的神经干细胞显著改善了锰暴露小鼠在莫里斯水迷宫中的空间学习和记忆功能。免疫荧光分析表明,一些存活的神经干细胞分化为神经元或胶质细胞,它们可能已在功能上整合到受损的局部回路中,为移植神经干细胞的小鼠认知功能改善提供了可能的细胞基础。综上所述,我们的研究结果证实了锰诱导的脑内神经发生损伤,并强调了通过神经干细胞移植治疗锰暴露的潜力,为对抗这种类型的神经毒性提供了一种切实可行的治疗策略。

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