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Effects of BDNF-Transfected BMSCs on Neural Functional Recovery and Synaptophysin Expression in Rats with Cerebral Infarction

机译:BDNF转染BMSCs对脑梗死大鼠神经功能回收和突触蛋白表达的影响

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摘要

The purpose of this study was to investigate the effects of brain-derived neurotrophic factor (BDNF)-transfected bone marrow mesenchymal stem cells (BMSCs) on neural functional recovery and synaptophysin expression in rats with cerebral infarction (CI). A total of 120 healthy Sprague Dawley rats were randomly divided into sham group, control group, and model group. Craniotomy was conducted and neurological function defect scoring was used to verify the model. BDNF containing recombinant plasmid was transfected into rat BMSCs, which was verified by flow cytometry and Western Blot. After injection of the transfected BMSCs, neural functional recovery of the CI rats and synaptophysin expression were measured. After the CI rat model was established, magnetic resonance (MR) imaging, 2, 3, 5- triphenyl tetrazolium chloride (TTC) staining, and the neurological function defect scoring determined the success of the model. CD34 (-), CD45 (-), CD29 (+), and CD90 (+) cells detected showed that the obtained BMSCs have high purity. BDNF protein was highly expressed in the BMSCs successfully transfected with the recombinant plasmid. Balance beam walking score, rotating bar walking score, and screen test score were significantly lower, while synaptophysin expression was higher in the BDNF model group than those in the non-BDNF model group and sham group with time extension. BDNF can increase synaptic plasticity and neurogenesis and have a promotional role in neural functional recovery and synaptophysin expression in rats with CI. BDNF-transfected BMSCs may therefore have better treatment efficacy for CI clinically.
机译:本研究的目的是探讨脑衍生的神经营养因子(BDNF) - 转发骨髓间充质干细胞(BMSC)对脑梗死大鼠神经功能回收和突触菌蛋白表达的影响(CI)。总共120只健康的Sprague Dawley大鼠随机分为假组,对照组和模型组。进行了Craniotomy,并使用神经功能缺陷评分来验证模型。将含有重组质粒的BDNF转染到大鼠BMSC中,通过流式细胞术和Western印迹验证。在注射转染的BMSC后,测量CI大鼠和突触甘油表达的神经功能恢复。在建立CI大鼠模型之后,磁共振(MR)成像,2,3,5-三苯基四唑(TTC)染色和神经功能缺陷评分确定了模型的成功。检测到CD34( - ),CD45( - ),CD29(+)和CD90(+)细胞显示所获得的BMSC具有高纯度。在成功用重组质粒转染的BMSC中高度表达BDNF蛋白。平衡梁行走分数,旋转杆行走分数和筛网测试得分显着降低,而BDNF模型组在非BDNF模型组和假手段中的突出模型组中的突触蛋白表达较高。 BDNF可以增加突触可塑性和神经发生,并且在CI大鼠中具有促进作用。因此,BDNF转染的BMSC临床上具有更好的CI治疗疗效。

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