Human Neural Stem Cells Reinforce Hippocampal Synaptic Network and Rescue Cognitive Deficits in a Mouse Model of Alzheimer's Disease

被引:35
|
作者
Zhang, Ting [1 ]
Ke, Wei [2 ,3 ]
Zhou, Xuan [4 ]
Qian, Yun [1 ]
Feng, Su [1 ]
Wang, Ran [1 ]
Cui, Guizhong [1 ]
Tao, Ran [1 ]
Guo, Wenke [1 ,6 ]
Duan, Yanhong [4 ]
Zhang, Xiaobing [5 ]
Cao, Xiaohua [4 ]
Shu, Yousheng [2 ,3 ]
Yue, Chunmei [1 ]
Jing, Naihe [1 ,6 ,7 ]
机构
[1] Univ Chinese Acad Sci, Shanghai Inst Biochem & Cell Biol, CAS Ctr Excellence Mol Cell Sci, State Key Lab Cell Biol,Chinese Acad Sci, 320 Yue Yang Rd, Shanghai 200031, Peoples R China
[2] Beijing Normal Univ, State Key Lab Cognit Neurosci & Learning, 19 Xinjiekou Wai St, Beijing 100875, Peoples R China
[3] Beijing Normal Univ, IDG McGovern Inst Brain Res, 19 Xinjiekou Wai St, Beijing 100875, Peoples R China
[4] East China Normal Univ, Shanghai Key Lab Brain Funct Genom, Key Lab Brain Funct Genom, Minist Educ,Sch Life Sci, Shanghai, Peoples R China
[5] Loma Linda Univ, Dept Med, Div Regenerat Med, Loma Linda, CA 92350 USA
[6] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
[7] Chinese Acad Sci, Inst Stem Cell & Regenerat, Beijing 100101, Peoples R China
来源
STEM CELL REPORTS | 2019年 / 13卷 / 06期
基金
中国国家自然科学基金;
关键词
BLOOD MONONUCLEAR-CELLS; IMPROVE COGNITION; DIRECT CONVERSION; TRANSGENIC MODEL; INTEGRATION-FREE; MEMORY DEFICITS; FIBROBLASTS; GENERATION; PLASTICITY; CORTEX;
D O I
10.1016/j.stemcr.2019.10.012
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Alzheimer's disease (AD) is characterized by memory impairments in its earliest clinical phase. The synaptic loss and dysfunction leading to failures of synaptic networks in AD brain directly cause cognitive deficits of patient. However, it remains unclear whether the synaptic networks in AD brain could be repaired. In this study, we generated functional human induced neural progenitor/stem cells (iNPCs) that had been transplanted into the hippocampus of immunodeficient wild-type and AD mice. The grafted human iNPCs efficiently differentiated into neurons that displayed long-term survival, progressively acquired mature membrane properties, formed graft-host synaptic connections with mouse neurons and functionally integrated into local synaptic circuits, which eventually reinforced and repaired the neural networks of host hippocampus. Consequently, AD mice with human iNPCs exhibited enhanced synaptic plasticity and improved cognitive abilities. Together, our results suggest that restoring synaptic failures by stem cells might provide new directions for the development of novel treatments for human AD.
引用
收藏
页码:1022 / 1037
页数:16
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