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电针对促进移植的 TrkC 修饰间充质干细胞衍生的神经网络整合到大鼠横断脊髓中的作用机制是通过增加神经营养因子-3。

Electroacupuncture facilitates the integration of a grafted TrkC-modified mesenchymal stem cell-derived neural network into transected spinal cord in rats via increasing neurotrophin-3.

机构信息

Key Laboratory for Stem Cells and Tissue Engineering, Ministry of Education, Sun Yat-sen University, Guangzhou, China.

Department of Histology and Embryology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.

出版信息

CNS Neurosci Ther. 2021 Jul;27(7):776-791. doi: 10.1111/cns.13638. Epub 2021 Mar 24.

DOI:10.1111/cns.13638
PMID:33763978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8193704/
Abstract

AIMS

This study was aimed to investigate whether electroacupuncture (EA) would increase the secretion of neurotrophin-3 (NT-3) from injured spinal cord tissue, and, if so, whether the increased NT-3 would promote the survival, differentiation, and migration of grafted tyrosine kinase C (TrkC)-modified mesenchymal stem cell (MSC)-derived neural network cells. We next sought to determine if the latter would integrate with the host spinal cord neural circuit to improve the neurological function of injured spinal cord.

METHODS

After NT-3-modified Schwann cells (SCs) and TrkC-modified MSCs were co-cultured in a gelatin sponge scaffold for 14 days, the MSCs differentiated into neuron-like cells that formed a MSC-derived neural network (MN) implant. On this basis, we combined the MN implantation with EA in a rat model of spinal cord injury (SCI) and performed immunohistochemical staining, neural tracing, electrophysiology, and behavioral testing after 8 weeks.

RESULTS

Electroacupuncture application enhanced the production of endogenous NT-3 in damaged spinal cord tissues. The increase in local NT-3 production promoted the survival, migration, and maintenance of the grafted MN, which expressed NT-3 high-affinity TrkC. The combination of MN implantation and EA application improved cortical motor-evoked potential relay and facilitated the locomotor performance of the paralyzed hindlimb compared with those of controls. These results suggest that the MN was better integrated into the host spinal cord neural network after EA treatment compared with control treatment.

CONCLUSIONS

Electroacupuncture as an adjuvant therapy for TrkC-modified MSC-derived MN, acted by increasing the local production of NT-3, which accelerated neural network reconstruction and restoration of spinal cord function following SCI.

摘要

目的

本研究旨在探讨电针对损伤脊髓组织神经营养因子-3(NT-3)分泌的影响,以及增加的 NT-3 是否促进酪氨酸激酶 C(TrkC)修饰的间充质干细胞(MSC)衍生的神经网络细胞的存活、分化和迁移。接下来,我们试图确定后者是否会与宿主脊髓神经回路整合,以改善损伤脊髓的神经功能。

方法

将 NT-3 修饰的雪旺细胞(SCs)和 TrkC 修饰的 MSC 共培养在明胶海绵支架上 14 天后,MSC 分化为神经元样细胞,形成 MSC 衍生的神经网络(MN)植入物。在此基础上,我们将 MN 植入物与脊髓损伤(SCI)大鼠模型中的电针相结合,在 8 周后进行免疫组织化学染色、神经示踪、电生理学和行为测试。

结果

电针应用增强了损伤脊髓组织中内源性 NT-3 的产生。局部 NT-3 产生的增加促进了移植 MN 的存活、迁移和维持,MN 表达 NT-3 高亲和力 TrkC。MN 植入物与电针联合应用改善了皮质运动诱发电位的传递,并促进了瘫痪后肢的运动性能,与对照组相比。这些结果表明,与对照组相比,电针治疗后 MN 更好地整合到宿主脊髓神经网络中。

结论

电针作为 TrkC 修饰的 MSC 衍生 MN 的辅助治疗方法,通过增加局部 NT-3 的产生,加速了 SCI 后神经网络的重建和脊髓功能的恢复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/30fcda75c377/CNS-27-776-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/04bd9de1d72d/CNS-27-776-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/b4012239ea0d/CNS-27-776-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/968f676f3418/CNS-27-776-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/24422b323650/CNS-27-776-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/8b33a3b7103e/CNS-27-776-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/30fcda75c377/CNS-27-776-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/04bd9de1d72d/CNS-27-776-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/b4012239ea0d/CNS-27-776-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/968f676f3418/CNS-27-776-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/24422b323650/CNS-27-776-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/8b33a3b7103e/CNS-27-776-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b5/8193704/30fcda75c377/CNS-27-776-g006.jpg

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