首页> 外文期刊>Journal of Molecular Neuroscience: MN >Buyang Huanwu Decoction (BYHWD) Enhances Angiogenic Effect of Mesenchymal Stem Cell by Upregulating VEGF Expression After Focal Cerebral Ischemia
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Buyang Huanwu Decoction (BYHWD) Enhances Angiogenic Effect of Mesenchymal Stem Cell by Upregulating VEGF Expression After Focal Cerebral Ischemia

机译:补阳还五汤(BYHWD)通过上调局灶性脑缺血后VEGF的表达增强间充质干细胞的血管生成作用

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摘要

Buyang Huanwu decoction (BYHWD) has been used for centuries to treat paralysis and stroke. Previously, we have demonstrated that BYHWD combined with mesenchymal stem cell (MSC) transplantation attenuates ischemic injury partly by upregulating angiogenesis. However, the mechanisms of this drug for stroke treatment are not completely understood. Here, we aimed to clarify the mechanism of BYHWD on angiogenesis mediated by MSCs. Firstly, we verified microvessels with a size of 50-100 nm produced by either MSCs or MSCs treated by 500 mu g/ml BYHWD. These exosomes were purified and found to be able to activate vascular endothelial growth factor (VEGF) expression in endothelial cells (ECs). Moreover, exosomes from MSCs and MSCs treated by BYHWD induced elevated microRNA (miRNA)-126 expression and reduced miR-221 and miR-222 expression. In MSCs, disruption of dicer, an enzyme responsible for miRNA maturation, by dicer small interfering RNA (siRNA), or RNase pretreatment abolished this ability of the exosomes. Additionally, exosomes from MSCs treated by BYHWD promoted VEGF and Ki-67 expression and augmented vascular density in rat brain after bilateral carotid artery ligation. In conclusion, our study revealed that BYHWD exposure augmented angiogenetic miRNA and VEGF expression in exosomes secreted by MSCs and elevated angiogenesis in rat brain.
机译:补阳还五汤(BYHWD)已被用于治疗瘫痪和中风已有数百年历史。以前,我们已经证明BYHWD结合间充质干细胞(MSC)移植可部分通过上调血管生成来减轻局部缺血性损伤。但是,该药物用于中风治疗的机制尚未完全了解。在这里,我们旨在阐明BYHWD对MSC介导的血管生成的机制。首先,我们验证了由MSC或经500μg / ml BYHWD处理的MSC产生的大小为50-100 nm的微血管。这些外泌体经过纯化,发现能够激活内皮细胞(EC)中的血管内皮生长因子(VEGF)表达。此外,来自MSC和BYHWD处理的MSC的外泌体诱导了升高的microRNA(miRNA)-126表达并降低了miR-221和miR-222表达。在MSC中,通过切丁酶小分子干扰RNA(siRNA)或RNase预处理破坏切丁酶(一种负责miRNA成熟的酶),从而消除了外泌体的这种能力。此外,在双侧颈动脉结扎后,通过BYHWD处理的MSC的外泌体促进了大鼠脑中VEGF和Ki-67的表达并增强了血管密度。总之,我们的研究表明,BYHWD暴露可增加MSC分泌的外泌体中血管生成性miRNA和VEGF的表达,并增加大鼠脑血管生成。

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