Hollenberg Morley D
Department of Physiology & Pharmacology and Department of Medicine, University of Calgary Faculty of Medicine, Calgary, AB, Canada T2N 4N1.
Clin Invest Med. 2010 Apr 1;33(2):E133. doi: 10.25011/cim.v33i2.12352.
This article provides a personalized overview of the role of proteinases in generating hormone-like cell signals. Also outlined is the unexpected route of discovery that led one investigator over a four-decade time span, from early studies of the interactions of oxytocin and vasopressin with their neurophysin binding proteins to current studies of the tethered ligand activation mechanism that is unique for the G-protein-coupled family of proteinase-activated receptors (PARs). The focus is not only on the intriguing PAR receptor family, but also on alternative mechanisms whereby proteinases activate signal transduction pathways. Also summarized are the potential physiological and pathophysiological roles that PARs may play in the setting of inflammatory disorders ranging from arthritis to colitis. The therapeutic implications of considering PARs as drug targets are also discussed.
本文提供了关于蛋白酶在产生激素样细胞信号中作用的个性化概述。还概述了一条意外的发现路径,该路径引领一位研究人员在四十年的时间跨度内,从催产素和血管加压素与其神经垂体素结合蛋白相互作用的早期研究,到目前对蛋白酶激活受体(PARs)的G蛋白偶联家族所特有的拴系配体激活机制的研究。重点不仅在于引人入胜的PAR受体家族,还在于蛋白酶激活信号转导途径的替代机制。还总结了PARs在从关节炎到结肠炎等炎症性疾病中可能发挥的潜在生理和病理生理作用。还讨论了将PARs视为药物靶点的治疗意义。