Neuro-vascular link: from genetic insights to therapeutic perspectives.

P Carmeliet
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Abstract

Understanding the molecular basis of the formation of blood vessels (angiogenesis) and nerves (neurogenesis) is of great medical relevance. It is well known that dysregulation of angiogenesis leads to tissue ischemia, cancer, inflammation and other disorders, while a dysfunction of the nerve system contributes to motorneuron disorders like amyotrophic lateral sclerosis (ALs) and other neurodegenerative diseases. The observations of Andreas Vesalius--Belgian anatomist of the 16th century--that patterning ofvessels and nerves show more than remarkable similarities, are currently revisited in exciting studies. Indeed, often, vessels and nerves even track alongside each other. Recent genetic studies revealed that vessels and nerves share many more common principles and signals for navigation, proliferation and survival than previously suspected. For instance, gene inactivation studies in mice and zebrafish showed that axon guidance signals regulate vessel navigation. Conversely, prototypic angiogenic factors such as VEGF control neurogenesis and regulate axon and neuron guidance, independently of their angiogenic activity. The next coming years promise to become an exciting journey to further unravel the molecular basis and explore the therapeutic potential of the neurovascular link.

神经血管联系:从遗传学的见解到治疗的观点。
了解血管(血管生成)和神经(神经发生)形成的分子基础具有重要的医学意义。众所周知,血管生成的失调会导致组织缺血、癌症、炎症等疾病,而神经系统的功能障碍会导致肌萎缩性侧索硬化症(ALs)等运动神经元疾病和其他神经退行性疾病。16世纪的比利时解剖学家安德烈亚斯·维萨里乌斯(Andreas Vesalius)观察到,血管和神经的模式表现出惊人的相似之处,目前在令人兴奋的研究中被重新审视。事实上,血管和神经甚至经常彼此相邻。最近的基因研究表明,血管和神经在导航、增殖和生存方面分享的共同原理和信号比以前所怀疑的要多得多。例如,对小鼠和斑马鱼的基因失活研究表明,轴突引导信号调节血管导航。相反,原型血管生成因子如VEGF控制神经发生,调节轴突和神经元的引导,独立于它们的血管生成活性。接下来的几年有望成为一个令人兴奋的旅程,进一步解开分子基础,探索神经血管联系的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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