间充质干细胞
肝细胞生长因子
衰老
神经科学
干细胞
神经干细胞
海马体
PI3K/AKT/mTOR通路
细胞生物学
生物
蛋白激酶B
癌症研究
医学
信号转导
生物化学
受体
作者
Yi Jia,Ning Cao,Jinglei Zhai,Quan Zeng,Pei zheng Zheng,Ruyu Su,Tuling Liao,Jiajing Liu,Haiyun Pei,Zeng Fan,Junnian Zhou,Jiafei Xi,Lijuan He,Lin Chen,Xue Nan,Wen Yue,Xuetao Pei
标识
DOI:10.1002/advs.201903809
摘要
Stem cells have emerged as a potential therapy for a range of neural insults, but their application in Alzheimer's disease (AD) is still limited and the mechanisms underlying the cognitive benefits of stem cells remain to be elucidated. Here, the effects of clinical-grade human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) on the recovery of cognitive ability in SAMP8 mice, a senescence-accelerated mouse model of AD is explored. A functional assay identifies that the core functional factor hepatocyte growth factor (HGF) secreted from hUC-MSCs plays critical roles in hUC-MSC-modulated recovery of damaged neural cells by down-regulating hyperphosphorylated tau, reversing spine loss, and promoting synaptic plasticity in an AD cell model. Mechanistically, structural and functional recovery, as well as cognitive enhancements elicited by exposure to hUC-MSCs, are at least partially mediated by HGF in the AD hippocampus through the activation of the cMet-AKT-GSK3β signaling pathway. Taken together, these data strongly implicate HGF in mediating hUC-MSC-induced improvements in functional recovery in AD models.
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