首页> 外文期刊>Experimental Neurology >Diffuse and persistent blood-spinal cord barrier disruption after contusive spinal cord injury rapidly recovers following intravenous infusion of bone marrow mesenchymal stem cells
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Diffuse and persistent blood-spinal cord barrier disruption after contusive spinal cord injury rapidly recovers following intravenous infusion of bone marrow mesenchymal stem cells

机译:静脉注射骨髓间充质干细胞后,挫伤性脊髓损伤后弥漫性和持续性血脊髓屏障破坏迅速恢复

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Intravenous infusion of mesenchymal stem cells (MSCs) has been shown to reduce the severity of experimental spinal cord injury (SCI), but mechanisms are not fully understood. One important consequence of SCI is damage to the microvasculature and disruption of the blood spinal cord barrier (BSCB). In the present study we induced a contusive SCI at T9 in the rat and studied the effects of intravenous MSC infusion on BSCB permeability, microvascular architecture and locomotor recovery over a 10 week period. Intravenously delivered MSCs could not be identified in the spinal cord, but distributed primarily to the lungs where they survived for a couple of days. Spatial and temporal changes in BSCB integrity were assessed by intravenous infusions of Evans blue (EvB) within vivo and ex vivo optical imaging and spectrophotometric quantitation of EvB leakage into the parenchyma. SCI resulted in prolonged BSCB leakage that was most severe at the impact site but disseminated extensively rostral and caudal to the lesion over 6 weeks. Contused spinal cords also showed an increase in vessel size, reduced vessel number, dissociation of pericytes from microvessels and decreases in von Willebrand factor (vWF) and endothelial barrier antigen (EBA) expression. In MSC-treated rats, BSCB leakage was reduced, vWF expression was increased and locomotor function improved beginning 1 week post-MSC infusion, i.e., 2 weeks post-SCI. These results suggest that intravenously delivered MSCs have important effects on reducing BSCB leakage which could contribute to their therapeutic efficacy. (C) 2015 Published by Elsevier Inc.
机译:静脉内注射间充质干细胞(MSCs)可以降低实验性脊髓损伤(SCI)的严重程度,但机理尚不完全清楚。 SCI的重要后果之一是对微脉管系统的损害以及对血液脊髓屏障(BSCB)的破坏。在本研究中,我们在大鼠的T9处诱导了挫伤性SCI,并研究了静脉MSC输注对BSCB渗透性,微血管结构和运动恢复的作用,历时10周。不能在脊髓中识别出静脉内递送的MSC,但主要分布在它们可以存活几天的肺中。 BSCB完整性的时空变化是通过在体内和离体光学成像内静脉输注伊文思蓝(EvB)以及分光光度定量EvB泄漏到实质中来评估的。 SCI导致BSCB渗漏时间延长,这在撞击部位最为严重,但在6周内广泛散布到病变的喙状和尾状。挫伤的脊髓还显示出血管大小的增加,血管数目的减少,周细胞与微血管的分离以及血管性血友病因子(vWF)和内皮屏障抗原(EBA)表达的降低。在MSC治疗的大鼠中,BSCB渗漏减少,vWF表达增加,运动功能改善,在MSC输注后1周即SCI后2周开始。这些结果表明,静脉内递送的MSC对减少BSCB渗漏具有重要作用,这可能有助于其治疗功效。 (C)2015年由Elsevier Inc.出版

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