Institute for Regenerative Medicine, University of Zurich, 8952, Schlieren, Zurich, Switzerland.
Dept. of Health Sciences and Technology, ETH Zurich, 8092, Zurich, Switzerland.
Sci Rep. 2019 Dec 27;9(1):20040. doi: 10.1038/s41598-019-56634-1.
Angiogenesis is a key restorative process following stroke but has also been linked to increased vascular permeability and blood brain barrier (BBB) disruption. Previous pre-clinical approaches primarily focused on the administration of vascular endothelial growth factor (VEGF) to promote vascular repair after stroke. Although shown to improve angiogenesis and functional recovery from stroke, VEGF increased the risk of blood brain barrier disruption and bleedings to such an extent that its clinical use is contraindicated. As an alternative strategy, antibodies against the neurite growth inhibitory factor Nogo-A have recently been shown to enhance vascular regeneration in the ischemic central nervous system (CNS); however, their effect on vascular permeability is unknown. Here, we demonstrate that antibody-mediated Nogo-A neutralization following stroke has strong pro-angiogenic effects but does not increase vascular permeability as opposed to VEGF. Moreover, VEGF-induced vascular permeability was partially prevented when VEGF was co-administered with anti-Nogo-A antibodies. This study may provide a novel therapeutic strategy for vascular repair and maturation in the ischemic brain.
血管生成是中风后恢复的关键过程,但也与血管通透性增加和血脑屏障(BBB)破坏有关。以前的临床前方法主要集中在血管内皮生长因子(VEGF)的给药上,以促进中风后的血管修复。尽管 VEGF 已被证明可改善血管生成和中风后的功能恢复,但它增加了血脑屏障破坏和出血的风险,以至于其临床应用被禁止。作为一种替代策略,最近已经证明针对神经突生长抑制因子 Nogo-A 的抗体可以增强缺血性中枢神经系统(CNS)中的血管再生;然而,它们对血管通透性的影响尚不清楚。在这里,我们证明中风后抗体介导的 Nogo-A 中和具有很强的促血管生成作用,但与 VEGF 不同,不会增加血管通透性。此外,当 VEGF 与抗 Nogo-A 抗体共同给药时,部分预防了 VEGF 诱导的血管通透性增加。这项研究可能为缺血性大脑中的血管修复和成熟提供了一种新的治疗策略。