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人脑源性神经营养因子基因修饰的骨髓间充质干细胞联合促红细胞生成素可改善急性脊髓损伤。

Human Brain-Derived Neurotrophic Factor Gene-Modified Bone Marrow Mesenchymal Stem Cells Combined With Erythropoietin Can Improve Acute Spinal Cord Injury.

作者信息

Li YongLei, Wang Hongchen, Ding Xiaofang, Shen Jiancheng, Zhou Haitao, Jiang Dengxue, Jin Chen, Li Kuang

机构信息

Department of Orthopedics, Beijing Longfu Hospital, Beijing, China.

Beijing Daxing District Hospital of Integrated Chinese and Western Medicine, Beijing, China.

出版信息

Dose Response. 2020 Mar 30;18(1):1559325820910930. doi: 10.1177/1559325820910930. eCollection 2020 Jan-Mar.

Abstract

OBJECTIVE

To assess the effect as well as mechanism of bone marrow mesenchymal stem cells (BMSCs) modified by the human brain-derived neurotrophic factor gene combined with erythropoietin (EPO) in the treatment of acute spinal cord injury (SCI) in rats.

METHODS

The Brain-derived neurotrophic factor (BDNF) gene was transected by a virus vector. Rats with SCI were randomly split into following groups: The normal saline (NS) group, the EPO group, The Basso, Beattie, and Bresnahan scores, messenger RNA BDNF expression, and apoptosis rates were compared between the 4 groups at 1, 3, 7, 14, and 21 days after SCI.

RESULTS

At 7, 14, and 21 days after operation, the expression of the BDNF gene in the other 3 groups was higher than that of the NS group, and the difference was statistically significant ( < .05). The apoptosis rate in the combined group was less than that of NS, EPO, and BDNF/BMSC groups, and the differences were statistically significant ( < .05).

CONCLUSION

Brain-derived neurotrophic factor gene-modified BMSC transplantation combined with EPO can promote the repair of nerve function after SCI in rats.

摘要

目的

评估经人脑源性神经营养因子基因联合促红细胞生成素(EPO)修饰的骨髓间充质干细胞(BMSCs)对大鼠急性脊髓损伤(SCI)的治疗效果及机制。

方法

采用病毒载体转染脑源性神经营养因子(BDNF)基因。将脊髓损伤大鼠随机分为以下几组:生理盐水(NS)组、EPO组,比较脊髓损伤后1、3、7、14和21天4组之间的Basso、Beattie和Bresnahan评分、信使核糖核酸BDNF表达及凋亡率。

结果

术后7、14和21天,其他3组的BDNF基因表达均高于NS组,差异有统计学意义(<.05)。联合组的凋亡率低于NS组、EPO组和BDNF/BMSC组,差异有统计学意义(<.05)。

结论

脑源性神经营养因子基因修饰的BMSC移植联合EPO可促进大鼠脊髓损伤后神经功能的修复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7cd/7119236/f4387b2a302a/10.1177_1559325820910930-fig1.jpg

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