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静脉注射神经祖细胞促进脑缺血后血管生成。

Intravenous injection of neural progenitor cells facilitates angiogenesis after cerebral ischemia.

机构信息

Department of Molecular and Cellular Pharmacology, Tokyo University of Pharmacy and Life Sciences 1432-1 Horinouchi, Hachioji, Tokyo, 192-0392, Japan.

出版信息

Brain Behav. 2013 Mar;3(2):43-53. doi: 10.1002/brb3.113. Epub 2012 Dec 28.

Abstract

Earlier we demonstrated that the injection of neural progenitor cells (NPCs) has therapeutic potential for the improvement of learning dysfunction after cerebral ischemia. However, it remained to be clarified how transplantation of NPCs can improve ischemia-induced dysfunction. In this study, we examined whether intravenous injection of NPCs after cerebral ischemia could enhance angiogenesis by affecting the expression of angiogenic factors. The injection of NPCs on day 7 after cerebral ischemia enhanced angiogenesis on day 28. Vascular endothelial growth factor (VEGF) and its receptor VEGFR2 were increased in expression by the NPC injection. The level of angiopoietin-1 (Ang-1), an angiogenic factor, but not that of Ang-2, which acts as an antagonist for the Ang-1 receptor, was also increased on day 28. In addition, the expression of Ang-1 receptor Tie2 was enhanced in brain capillaries. Furthermore, the amounts of tight junctional proteins, which are in the blood-brain barrier and whose expression occurs downstream of Ang-1/Tie2 signaling, were increased by the NPC injection. These results suggest that the NPC injection promoted angiogenesis through Ang-1/Tie2 and/or VEGF/VEGFR2 signaling in brain capillaries after cerebral ischemia. Such signaling might have the potential for causing vascular stabilization and maturation for a long period after cerebral ischemia.

摘要

我们之前的研究表明,神经祖细胞(NPCs)的注射对改善脑缺血后学习功能障碍具有治疗潜力。然而,移植 NPCs 如何改善缺血引起的功能障碍仍需阐明。在这项研究中,我们研究了脑缺血后 NPCs 的静脉注射是否可以通过影响血管生成因子的表达来增强血管生成。脑缺血后第 7 天注射 NPCs 可增强第 28 天的血管生成。NPC 注射可增加血管内皮生长因子(VEGF)及其受体 VEGFR2 的表达。血管生成因子血管生成素-1(Ang-1)的水平也在第 28 天增加,但其拮抗剂血管生成素-2(Ang-2)的水平没有增加。此外,血管生成素-1 受体 Tie2 的表达在脑毛细血管中增强。此外,NPC 注射增加了血脑屏障中紧密连接蛋白的含量,而这些蛋白的表达是 Ang-1/Tie2 信号通路的下游。这些结果表明,NPC 注射通过脑缺血后血管内皮细胞中的 Ang-1/Tie2 和/或 VEGF/VEGFR2 信号促进了血管生成。这种信号可能具有在脑缺血后很长一段时间内引起血管稳定和成熟的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed69/3607146/20da441f0fbb/brb30003-0043-f3.jpg

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