TY - JOUR
T1 - Human Neural Stem Cells Reinforce Hippocampal Synaptic Network and Rescue Cognitive Deficits in a Mouse Model of Alzheimer's Disease
AU - Zhang, Ting
AU - Ke, Wei
AU - Zhou, Xuan
AU - Qian, Yun
AU - Feng, Su
AU - Wang, Ran
AU - Cui, Guizhong
AU - Tao, Ran
AU - Guo, Wenke
AU - Duan, Yanhong
AU - Zhang, Xiaobing
AU - Cao, Xiaohua
AU - Shu, Yousheng
AU - Yue, Chunmei
AU - Jing, Naihe
N1 - Publisher Copyright:
© 2019 The Authors
PY - 2019/12/10
Y1 - 2019/12/10
N2 - 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.
AB - 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.
KW - Alzheimer's disease
KW - cognitive improvement
KW - functional integration
KW - human induced neural progenitor cells
KW - synaptic networks
UR - http://www.scopus.com/inward/record.url?scp=85076449570&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85076449570&partnerID=8YFLogxK
U2 - 10.1016/j.stemcr.2019.10.012
DO - 10.1016/j.stemcr.2019.10.012
M3 - Article
C2 - 31761676
SN - 2213-6711
VL - 13
SP - 1022
EP - 1037
JO - Stem Cell Reports
JF - Stem Cell Reports
IS - 6
ER -