Lampropoulou Anastasia, Ruhrberg Christiana
*UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London EC1V 9EL, U.K.
Biochem Soc Trans. 2014 Dec;42(6):1623-8. doi: 10.1042/BST20140244.
Blood vessel formation during vertebrate development relies on a process called angiogenesis and is essential for organ growth and tissue viability. In addition, angiogenesis leads to pathological blood vessel growth in diseases with tissue ischaemia, such as neovascular eye disease and cancer. Neuropilin 1 (NRP1) is a transmembrane protein that serves as a receptor for the VEGF₁₆₅ isoform of the vascular endothelial growth factor (VEGF) to enhance cell migration during angiogenesis via VEGF receptor 2 (VEGFR2), and it is also essential for VEGF-induced vascular permeability and arteriogenesis. In addition, NRP1 activation affects angiogenesis independently of VEGF signalling by activating the intracellular kinase ABL1. NRP1 also acts as a receptor for the class 3 semaphorin (SEMA3A) to regulate vessel maturation during tumour angiogenesis and vascular permeability in eye disease. In the present paper, we review current knowledge of NRP1 regulation during angiogenesis and vascular pathology.
脊椎动物发育过程中的血管形成依赖于一个称为血管生成的过程,这对于器官生长和组织存活至关重要。此外,在诸如新生血管性眼病和癌症等伴有组织缺血的疾病中,血管生成会导致病理性血管生长。神经纤毛蛋白1(NRP1)是一种跨膜蛋白,作为血管内皮生长因子(VEGF)的VEGF₁₆₅亚型的受体,通过VEGF受体2(VEGFR2)增强血管生成过程中的细胞迁移,并且它对于VEGF诱导的血管通透性和动脉生成也至关重要。此外,NRP1的激活通过激活细胞内激酶ABL1独立于VEGF信号传导影响血管生成。NRP1还作为3类信号素(SEMA3A)的受体,在肿瘤血管生成过程中调节血管成熟以及在眼病中调节血管通透性。在本文中,我们综述了血管生成和血管病理学过程中NRP1调控的当前知识。