Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami School of Medicine, Miami, FL, 33136, USA.
Vascular Biology Institute, University of Miami School of Medicine, Miami, FL, 33136, USA.
Cell Mol Life Sci. 2018 Feb;75(4):635-647. doi: 10.1007/s00018-017-2635-5. Epub 2017 Aug 30.
Secretogranin III (Scg3) is a member of the granin protein family that regulates the biogenesis of secretory granules. Scg3 was recently discovered as an angiogenic factor, expanding its functional role to extrinsic regulation. Unlike many other known angiogenic factors, the pro-angiogenic actions of Scg3 are restricted to pathological conditions. Among thousands of quantified endothelial ligands, Scg3 has the highest binding activity ratio to diabetic vs. healthy mouse retinas and lowest background binding to normal vessels. In contrast, vascular endothelial growth factor binds to and stimulates angiogenesis of both diabetic and control vasculature. Consistent with its role in pathological angiogenesis, Scg3-neutralizing antibodies alleviate retinal vascular leakage in mouse models of diabetic retinopathy and retinal neovascularization in oxygen-induced retinopathy mice. This review summarizes our current knowledge of Scg3 as a regulatory protein of secretory granules, highlights its new role as a highly disease-selective angiogenic factor, and envisions Scg3 inhibitors as "selective angiogenesis blockers" for targeted therapy.
分泌颗粒蛋白 III(Scg3)是颗粒蛋白家族的一员,可调节分泌颗粒的生物发生。Scg3 最近被发现是一种血管生成因子,使其功能作用扩展到外在调节。与许多其他已知的血管生成因子不同,Scg3 的促血管生成作用仅限于病理状态。在数千种定量的内皮配体中,Scg3 与糖尿病 vs. 健康小鼠视网膜的结合活性比值最高,与正常血管的背景结合最低。相比之下,血管内皮生长因子与糖尿病和对照血管的血管生成均有结合并刺激作用。与它在病理性血管生成中的作用一致,Scg3 中和抗体可减轻糖尿病性视网膜病变小鼠模型中的视网膜血管渗漏和氧诱导性视网膜病变小鼠的视网膜新生血管形成。这篇综述总结了我们目前对 Scg3 作为分泌颗粒调节蛋白的认识,强调了其作为一种高度疾病选择性血管生成因子的新作用,并设想 Scg3 抑制剂是用于靶向治疗的“选择性血管生成阻断剂”。