Troger Josef, Theurl Markus, Kirchmair Rudolf, Pasqua Teresa, Tota Bruno, Angelone Tommaso, Cerra Maria C, Nowosielski Yvonne, Mätzler Raphaela, Troger Jasmin, Gayen Jaur R, Trudeau Vance, Corti Angelo, Helle Karen B
Department of Ophthalmology, Medical University of Innsbruck, Innsbruck, Austria.
Department of Internal Medicine, Medical University of Innsbruck, Innsbruck, Austria.
Prog Neurobiol. 2017 Jul;154:37-61. doi: 10.1016/j.pneurobio.2017.04.003. Epub 2017 Apr 22.
The granin family comprises altogether 7 different proteins originating from the diffuse neuroendocrine system and elements of the central and peripheral nervous systems. The family is dominated by three uniquely acidic members, namely chromogranin A (CgA), chromogranin B (CgB) and secretogranin II (SgII). Since the late 1980s it has become evident that these proteins are proteolytically processed, intragranularly and/or extracellularly into a range of biologically active peptides; a number of them with regulatory properties of physiological and/or pathophysiological significance. The aim of this comprehensive overview is to provide an up-to-date insight into the distribution and properties of the well established granin-derived peptides and their putative roles in homeostatic regulations. Hence, focus is directed to peptides derived from the three main granins, e.g. to the chromogranin A derived vasostatins, betagranins, pancreastatin and catestatins, the chromogranin B-derived secretolytin and the secretogranin II-derived secretoneurin (SN). In addition, the distribution and properties of the chromogranin A-derived peptides prochromacin, chromofungin, WE14, parastatin, GE-25 and serpinins, the CgB-peptide PE-11 and the SgII-peptides EM66 and manserin will also be commented on. Finally, the opposing effects of the CgA-derived vasostatin-I and catestatin and the SgII-derived peptide SN on the integrity of the vasculature, myocardial contractility, angiogenesis in wound healing, inflammatory conditions and tumors will be discussed.
嗜铬粒蛋白家族总共由7种不同的蛋白质组成,这些蛋白质源自弥散神经内分泌系统以及中枢和外周神经系统的组成部分。该家族以三种独特的酸性成员为主,即嗜铬粒蛋白A(CgA)、嗜铬粒蛋白B(CgB)和分泌粒蛋白II(SgII)。自20世纪80年代末以来,有一点已变得很明显,即这些蛋白质在颗粒内和/或细胞外被蛋白水解加工成一系列生物活性肽;其中许多具有生理和/或病理生理意义的调节特性。本综述的目的是提供关于成熟的嗜铬粒蛋白衍生肽的分布和特性及其在稳态调节中假定作用的最新见解。因此,重点关注源自三种主要嗜铬粒蛋白的肽,例如源自嗜铬粒蛋白A的血管抑制素、β-嗜铬粒蛋白、胰腺抑制素和酪蛋白抑制素,源自嗜铬粒蛋白B的分泌溶素以及源自分泌粒蛋白II的分泌神经肽(SN)。此外,还将对源自嗜铬粒蛋白A的肽原嗜铬粒蛋白、嗜铬真菌素、WE14、副抑制素、GE-25和丝氨酸蛋白酶抑制剂,CgB肽PE-11以及SgII肽EM66和曼色林的分布和特性进行评论。最后,将讨论源自CgA的血管抑制素-I和酪蛋白抑制素以及源自SgII的肽SN对脉管系统完整性、心肌收缩力、伤口愈合中的血管生成、炎症状态和肿瘤的相反作用。