Koul Sweaty, Fu Sherry, Koul Hari
Signal Transduction and Molecular Biology Laboratory, Division of Urology, Department of Surgery, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA.
Ann N Y Acad Sci. 2003 Dec;1010:292-5. doi: 10.1196/annals.1299.050.
Oxalate, a metabolic end product, is a major constituent of kidney stones. Previously, we and others have demonstrated that oxalate is toxic to renal epithelial cells. In the present study, we characterized oxalate-induced cell death in HK2 cells, a line of renal epithelial cells from the human kidney. For these studies, HK2 cells were exposed to oxalate for various time points. Cells were examined for nuclear morphology, DNA fragmentation, and expression of various apoptosis-related proteins. Apoptotic mode of cell death was also confirmed by TUNEL assay. Results from these studies revealed that oxalate exposure resulted in time-dependent increase in DNA fragmentation. Maximum DNA fragmentation was observed at 2-24 hours following oxalate exposure. Results from Western blot analysis demonstrated an increased expression of the FAS ligand. Taken together, these data reveal that oxalate-associated nephrotoxicity results from oxalate-induced apoptosis of renal epithelial cells.
草酸是一种代谢终产物,是肾结石的主要成分。此前,我们及其他研究人员已证明草酸对肾上皮细胞有毒性。在本研究中,我们对草酸诱导人肾来源的肾上皮细胞系HK2细胞死亡的情况进行了表征。在这些研究中,HK2细胞在不同时间点暴露于草酸中。检测细胞的核形态、DNA片段化以及各种凋亡相关蛋白的表达。TUNEL检测也证实了细胞死亡的凋亡模式。这些研究结果显示,草酸暴露导致DNA片段化随时间增加。草酸暴露后2至24小时观察到最大程度的DNA片段化。蛋白质印迹分析结果表明FAS配体的表达增加。综上所述,这些数据表明草酸相关的肾毒性是由草酸诱导的肾上皮细胞凋亡所致。