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Therapeutic effect of transplantation of human bone marrow-derived mesenchymal stem cells on neuron regeneration in a rat model of middle cerebral artery occlusion

机译:人骨髓间充质干细胞移植对大脑中动脉阻塞模型大鼠神经元再生的治疗作用

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摘要

Human bone marrow-derived mesenchymal stromal cells (hBMSCs) have been revealed to be beneficial for the regeneration of tissues and cells in several diseases. The present study aimed to elucidate the mechanisms underlying the effect of hBMSC transplantation on neuron regeneration in a rat model of middle cerebral artery occlusion (MCAO). The hBMSCs were isolated, cultured and identified. A rat model of MCAO was induced via the modified Longa method. Neurological severity scores (NSS) were adopted for the evaluation of neuronal function in the model rats after cell transplantation. Next, the expression levels of nestin, β-III-tubulin (β-III-Tub), glial fibrillary acidic protein (GFAP), HNA and neuronal nuclear antigen (NeuN) were examined, as well as the positive expression rates of human neutrophil alloantigen (HNA), nestin, NeuN, β-III-Tub and GFAP. The NSS, as well as the mRNA and protein expression of nestin, decreased at the 1st, 2nd, 4 and 8th weeks, while the mRNA and protein expression of NeuN, β-III-Tub and GFAP increased with time. In addition, after treatment, the MCAO rats showed decreased NSS and mRNA and protein expression of nestin, but elevated mRNA and protein expression of NeuN, β-III-Tub and GFAP at the 2nd, 4 and 8th weeks, and decreased positive expression of HNA and nestin with enhanced expression of NeuN, β-III-Tub and GFAP. Therefore, the present findings demonstrated that hBMSC transplantation triggered the formation of nerve cells and enhanced neuronal function in a rat model of MCAO.
机译:人骨髓来源的间充质基质细胞(hBMSCs)已被证明对多种疾病中组织和细胞的再生有益。本研究旨在阐明在大脑中动脉闭塞(MCAO)大鼠模型中,hBMSC移植对神经元再生的影响的潜在机制。分离,培养和鉴定了hBMSC。通过改良的Longa方法建立MCAO大鼠模型。采用神经系统严重程度评分(NSS)评估模型大鼠细胞移植后的神经元功能。接下来,检查巢蛋白,β-III-微管蛋白(β-III-Tub),神经胶质原纤维酸性蛋白(GFAP),HNA和神经元核抗原(NeuN)的表达水平,以及人中性粒细胞的阳性表达率同种抗原(HNA),巢蛋白,NeuN,β-III-Tub和GFAP。在第1、2、4和8周,NSS以及巢蛋白的mRNA和蛋白表达下降,而NeuN,β-III-Tub和GFAP的mRNA和蛋白表达随时间增加。此外,治疗后,MCAO大鼠在第2、4和8周时NSS和Nestin的mRNA和蛋白表达降低,但NeuN,β-III-Tub和GFAP的mRNA和蛋白表达升高,而在MAPK的表达则降低。 HNA和Nestin具有增强的NeuN,β-III-Tub和GFAP表达。因此,本研究结果表明,hBMSC移植在MCAO大鼠模型中触发了神经细胞的形成并增强了神经元功能。

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