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超声靶向微泡破坏介导血管生成基因治疗减少小鼠卒中后缺血性损伤。

Reduced ischemic injury after stroke in mice by angiogenic gene delivery via ultrasound-targeted microbubble destruction.

机构信息

From the Second Affiliated Hospital of Harbin Medical University, Harbin, China (H-BW, LY, LS, Jiang Wu, HT); and Toronto General Research Institute, University Health Network (H-BW, LY, Jun Wu, LS, RDW, R-KL); and Division of Cardiac Surgery, Department of Surgery, University of Toronto (H-BW, LY, Jun Wu, LS, RDW, R-KL), Toronto, Ontario, Canada.

出版信息

J Neuropathol Exp Neurol. 2014 Jun;73(6):548-58. doi: 10.1097/NEN.0000000000000077.

Abstract

Angiogenic gene therapy in patients with cerebral infarcts may have clinical benefit, but its potential is diminished by the difficulty of introducing genes into the brain. We evaluated the safety and efficacy of ultrasound-targeted microbubble destruction (UTMD) for delivery of genes to the brains of normal mice and after transient middle cerebral artery occlusion. In normal mice, disruption of the blood-brain barrier detected with trypan blue staining was reversible within 24 hours of a single UTMD administration. Expression of reporter genes in the brain after UTMD demonstrated successful targeted gene delivery and transfection. Decreased neurologic function after transient middle cerebral artery occlusion was attenuated versus controls at 7 days after UTMD delivery of vascular endothelial growth factor. Ultrasound-targeted microbubble destruction delivery of the VEGF gene resulted in decreased infarct areas, increased vessel density, and reduced apoptosis versus controls. There was no evidence of permanent brain injury throughout the study. Thus, UTMD was a safe, minimally invasive, effective technique for gene delivery to the brain. Vascular endothelial growth factor transfection of brain cells conferred beneficial effects on histopathologic parameters and neurologic function, and stimulated angiogenesis in a mouse stroke model.

摘要

血管生成基因治疗在脑梗死患者中可能具有临床获益,但由于将基因导入大脑的难度,其潜力受到限制。我们评估了超声靶向微泡破坏(UTMD)将基因递送至正常小鼠和短暂性大脑中动脉闭塞后大脑中的安全性和有效性。在正常小鼠中,用锥虫蓝染色检测到的血脑屏障破坏在单次 UTMD 给药后 24 小时内是可逆的。UTMD 后大脑中报告基因的表达表明成功地进行了靶向基因递送和转染。与对照组相比,UTMD 递送血管内皮生长因子(VEGF)后,短暂性大脑中动脉闭塞后的神经功能障碍在 7 天时得到减轻。与对照组相比,VEGF 基因的超声靶向微泡破坏传递导致梗死面积减少、血管密度增加和细胞凋亡减少。整个研究过程中均未发现永久性脑损伤的证据。因此,UTMD 是一种安全、微创、有效的脑内基因传递技术。脑内细胞的血管内皮生长因子转染对组织病理学参数和神经功能产生有益影响,并在小鼠中风模型中刺激血管生成。

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