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向大鼠和小鼠脑内动脉注射神经干细胞:在脑缺血中的应用

Intra-Arterial Delivery of Neural Stem Cells to the Rat and Mouse Brain: Application to Cerebral Ischemia.

作者信息

Zhang Bei, Joseph Binoy, Saatman Kathryn E, Chen Lei

机构信息

College of Public Health, Shaanxi University of Chinese Medicine.

Spinal Cord and Brain Injury Research Center, Department of Physiology, University of Kentucky.

出版信息

J Vis Exp. 2020 Jun 26(160). doi: 10.3791/61119.

Abstract

Neural stem cell (NSC) therapy is an emerging innovative treatment for stroke, traumatic brain injury and neurodegenerative disorders. As compared to intracranial delivery, intra-arterial administration of NSCs is less invasive and produces a more diffuse distribution of NSCs within the brain parenchyma. Further, intra-arterial delivery allows the first-pass effect in the brain circulation, lessening the potential for trapping of cells in peripheral organs, such as liver and spleen, a complication associated with peripheral injections. Here, we detail the methodology, in both mice and rats, for delivery of NSCs through the common carotid artery (mouse) or external carotid artery (rat) to the ipsilateral hemisphere after an ischemic stroke. Using GFP-labeled NSCs, we illustrate the widespread distribution achieved throughout the rodent ipsilateral hemisphere at 1 d, 1 week and 4 weeks after postischemic delivery, with a higher density in or near the ischemic injury site. In addition to long-term survival, we show evidence of differentiation of GFP-labeled cells at 4 weeks. The intra-arterial delivery approach described here for NSCs can also be used for administration of therapeutic compounds, and thus has broad applicability to varied CNS injury and disease models across multiple species.

摘要

神经干细胞(NSC)疗法是一种新兴的针对中风、创伤性脑损伤和神经退行性疾病的创新性治疗方法。与颅内给药相比,动脉内注射神经干细胞的侵入性较小,并且能使神经干细胞在脑实质内分布得更广泛。此外,动脉内给药可在脑循环中产生首过效应,减少细胞滞留在外周器官(如肝脏和脾脏)的可能性,而外周注射会出现这种并发症。在此,我们详细介绍在小鼠和大鼠中,通过颈总动脉(小鼠)或颈外动脉(大鼠)将神经干细胞输送到缺血性中风后同侧半球的方法。使用绿色荧光蛋白(GFP)标记的神经干细胞,我们展示了在缺血性给药后1天、1周和4周时,整个啮齿动物同侧半球实现的广泛分布,在缺血损伤部位或其附近密度更高。除了长期存活外,我们还展示了4周时绿色荧光蛋白标记细胞分化的证据。这里描述的神经干细胞动脉内输送方法也可用于治疗性化合物的给药,因此对多种物种的各种中枢神经系统损伤和疾病模型具有广泛的适用性。

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