Ebisuno S, Yoshida T, Kohjimoto Y, Ohkawa T
Department of Urology, Minami Wakayama National Hospital.
Nihon Hinyokika Gakkai Zasshi. 1993 Nov;84(11):1980-6. doi: 10.5980/jpnjurol1989.84.1980.
The present investigation was designed to study adhesion of calcium oxalate crystals on the surface of intact MDCK cells quantitatively, and to estimate the effects of glycosaminoglycans (GAGs) and cell injuries on these adhesions. Calcium oxalate monohydrate (COM) crystals adhere to the cell surface by an active force, and the attachment is in a time and concentration dependency with plateau. Pre-treatments with low concentration of GAGs (chondroitin sulphate C, hyaluronic acid, heparan sulphate, heparin and sodium pentosan polysulphate) produce significant reductions of the adhesion. There are significant decreases of the adhesions with pre-treatments of Triton-X100, 0.1 N HCl and gentamicin. These phenomena might be induced by some alterations of cell surface structures or characters. The current quantitative system on MDCK cells should serve as a useful model for the investigations of interactions with crystals and tubular cells. Our studies may also support the hypothesis of attachment of microcrystals to the cellular membrane, which is one of the most important and the earliest process of the pathophysiology of kidney stone.
本研究旨在定量研究草酸钙晶体在完整的MDCK细胞表面的黏附情况,并评估糖胺聚糖(GAGs)和细胞损伤对这些黏附的影响。一水合草酸钙(COM)晶体通过一种主动力黏附于细胞表面,且这种黏附具有时间和浓度依赖性,存在平台期。用低浓度的GAGs(硫酸软骨素C、透明质酸、硫酸乙酰肝素、肝素和聚戊糖硫酸酯钠)进行预处理可显著降低黏附。用Triton-X100、0.1 N HCl和庆大霉素进行预处理后,黏附也显著降低。这些现象可能是由细胞表面结构或特性的某些改变引起的。目前关于MDCK细胞的定量系统应可作为研究晶体与肾小管细胞相互作用的有用模型。我们的研究也可能支持微晶附着于细胞膜的假说,这是肾结石病理生理学中最重要且最早的过程之一。