首页> 外文期刊>Drug Design, Development and Therapy >Neuroprotective Effect of Mesenchymal Stromal Cell-Derived Extracellular Vesicles Against Cerebral Ischemia-Reperfusion-Induced Neural Functional Injury: A Pivotal Role for AMPK and JAK2/STAT3/NF-κB Signaling Pathway Modulation
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Neuroprotective Effect of Mesenchymal Stromal Cell-Derived Extracellular Vesicles Against Cerebral Ischemia-Reperfusion-Induced Neural Functional Injury: A Pivotal Role for AMPK and JAK2/STAT3/NF-κB Signaling Pathway Modulation

机译:间充质基质细胞源细胞间囊泡对脑缺血再灌注诱导的神经功能损伤的神经保护作用:AMPK和JAK2 / Stat3 / NF-κB信号传导途径调制的关键作用

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Introduction: Cerebral ischemia-reperfusion injury (CIRI) is the main factor that leads to poor prognosis of cerebral ischemia. Apoptosis has been shown to occur during the process of CIRI. Extracellular vesicles derived from mesenchymal stromal cells (MSCs-EVs) have shown broad potential for treating brain dysfunction and eliciting neuroprotective effects after stroke through neurogenesis and angiogenesis. However, the mechanism of action of extracellular vesicles during CIRI is not well known. Methods: A middle cerebral artery occlusion (MCAO) model was induced by the modified Longa method, and MSCs-EVs were injected via the tail vein. Results: Our results showed that MSCs-EVs significantly alleviated neurological deficits, reduced the volume of cerebral infarction and brain water content, improved pathological lesions in cortical brain tissue, and attenuated neuronal apoptosis in the cortex at 24 h and 48 h after MCAO in rats. Western blotting analysis showed that MSCs-EVs significantly upregulated p-AMPK and downregulated p-JAK2, p-STAT3 and p-NF-κB. In addition, an AMPK pathway blocker reversed the effect of MSCs-EVs on brain damage. Conclusion: These results indicate that MSCs-EVs protected MCAO-injured rats, possibly by regulating the AMPK and JAK2/STAT3/NF-κB signaling pathways. This study supports the use of MSCs-EVs as a potential treatment strategy for MCAO in the future.
机译:介绍:脑缺血再灌注损伤(CIRI)是导致脑缺血预后不良的主要因素。在Ciri过程中已经显示出发生的细胞凋亡。来自间充质基质细胞(MSCS-EVS)的细胞外囊泡显示出脑功能障碍和通过神经发生和血管生成后卒中后引发神经保护作用的广泛电位。然而,在CIRI期间细胞外囊泡的作用机制是不公知的。方法:通过修饰的LONGA方法诱导中脑动脉闭塞(MCAO)模型,通过尾静脉注射MSCS-EV。结果:我们的研究结果表明,MSCS-eV显着缓解了神经系统缺陷,减少了脑梗死和脑含水量的体积,改善了皮质脑组织中的病理病变,并在大鼠MCAO后24小时和48小时减毒神经元细胞凋亡。 Western印迹分析表明,MSCS-EVS显着上调的P-AMPK和下调的P-JAK2,P-STAT3和P-NF-κB。此外,AMPK途径阻滞剂逆转了MSCS-EVS对脑损伤的影响。结论:这些结果表明,MSCS-EVS保护了MCAO损伤的大鼠,可能是通过调节AMPK和JAK2 / Stat3 / NF-κB信号传导途径。本研究支持未来使用MSCS-EV作为MCAO的潜在治疗战略。

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