神经干细胞
脊髓损伤
神经发生
脊髓
移植
干细胞
内生
细胞生物学
生物
神经科学
医学
外科
生物化学
作者
Yaming Yang,Yongheng Fan,Haipeng Zhang,Qi Zhang,Yannan Zhao,Zhifeng Xiao,Wenbin Liu,Bing Chen,Lin Gao,Zheng Sun,Xiaoyu Xue,Muya Shu,Jianwu Dai
出处
期刊:Biomaterials
[Elsevier]
日期:2021-02-01
卷期号:269: 120479-120479
被引量:98
标识
DOI:10.1016/j.biomaterials.2020.120479
摘要
Complete spinal cord injury (SCI) leads to cell death, interruption of axonal connections and permanent functional impairments. In the development of SCI treatments, cell transplantation combined with biomaterial-growth factor-based therapies have been widely studied. Another avenue worth exploring is the generation of neurons from endogenous neural stem cells (NSCs) or reactive astrocytes activated by SCI. Here, we screened a combination of four small molecules, LDN193189, SB431542, CHIR99021 and P7C3-A20, that can increase neuronal differentiation of mouse and rat spinal cord NSCs. Moreover, the small molecules loaded in an injectable collagen hydrogel induced neurogenesis and inhibited astrogliogenesis of endogenous NSCs in the injury site, which usually differentiate into astrocytes under pathological conditions. Meanwhile, induced neurons migrated into the non-neural lesion core, and genetic fate mapping showed that neurons mainly originated from NSCs in the parenchyma, but not from the central canal of the spinal cord. The neuronal regeneration in the lesion sites resulted in some recovery of locomotion. Our findings indicate that the combined treatment of small molecules and collagen hydrogel is a potential therapeutic strategy for SCI by inducing in situ endogenous NSCs to form neurons and restore damaged functions.
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