脊髓损伤
神经干细胞
PI3K/AKT/mTOR通路
移植
小胶质细胞
脊髓
蛋白激酶B
神经保护
神经科学
干细胞
医学
细胞凋亡
药理学
化学
炎症
免疫学
外科
细胞生物学
生物
生物化学
作者
W. Zhang,Mingshan Liu,Jie Ren,Shuwei Han,Xiaolong Zhou,Dapeng Zhang,Xianzheng Guo,Haiwen Feng,Lei Ye,Shiqing Feng,Xizi Song,Lin Jin,Wei Wang
标识
DOI:10.1002/advs.202308993
摘要
Abstract Neural stem cells (NSCs) transplantation is an attractive and promising treatment strategy for spinal cord injury (SCI). Various pathological processes including the severe inflammatory cascade and difficulty in stable proliferation and differentiation of NSCs limit its application and translation. Here, a novel physico‐chemical bifunctional neural stem cells delivery system containing magnetic nanoparticles (MNPs and methylprednisolone (MP) is designed to repair SCI, the former regulates NSCs differentiation through magnetic mechanical stimulation in the chronic phase, while the latter alleviates inflammatory response in the acute phase. The delivery system releases MP to promote microglial M2 polarization, inhibit M1 polarization, and reduce neuronal apoptosis. Meanwhile, NSCs tend to differentiate into functional neurons with magnetic mechanical stimulation generated by MNPs in the static magnetic field, which is related to the activation of the PI3K/AKT/mTOR pathway. SCI mice achieve better functional recovery after receiving NSCs transplantation via physico‐chemical bifunctional delivery system, which has milder inflammation, higher number of M2 microglia, more functional neurons, and axonal regeneration. Together, this bifunctional NSCs delivery system combined physical mechanical stimulation and chemical drug therapy is demonstrated to be effective, which provides new treatment insights into clinical transformation of SCI repair.
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