Edelstein C L, Ling H, Gengaro P E, Nemenoff R A, Bahr B A, Schrier R W
Department of Medicine, University of Colorado School of Medicine, Denver, USA.
Kidney Int. 1997 Nov;52(5):1271-8. doi: 10.1038/ki.1997.452.
The effect of glycine on hypoxia- and ionomycin-induced increases in calpain activity in rat proximal tubules was determined. Calpain activity was determined both in vitro and in the intact cell using the fluorescent substrate N-succinyl-Leu-Leu-Val-Tyr-7-amido-4-methyl coumarin (N-succinyl-Leu-Leu-Val-Tyr-AMC) and Western blotting for calpain-specific spectrin breakdown products (BDP), respectively. At 7.5 minutes of hypoxia (prelethal injury model) there was a significant (10-fold) increase in in vitro calpain activity that was not inhibited by glycine. At 15 minutes of hypoxia (postlethal injury model) there was a further increase in calpain activity that was inhibited by glycine. Normoxic tubules incubated with the calcium ionophore ionomycin (5 microM) for two minutes and 10 minutes had a significant increase in calpain activity that was not inhibited by glycine. After 15 minutes of hypoxia in the presence of glycine, there was an increase in calpain-specific spectrin breakdown products (BDP) in both Triton X-100 soluble and cytosolic extracts from proximal tubules. Glycine in concentrations up to 10 mM had no direct effect on the in vitro calpain activity of purified calpains. The present study demonstrates that: (1) prelethal increases in calpain activity stimulated by hypoxia and ionomycin treatment are not affected by glycine; (2) calpain-mediated spectrin breakdown during hypoxia occurs in the presence of glycine; (3) glycine does prevent the additional postlethal increase in calpain activity probably by maintaining membrane integrity to calcium influx.
研究了甘氨酸对大鼠近端肾小管中缺氧和离子霉素诱导的钙蛋白酶活性增加的影响。分别使用荧光底物N-琥珀酰-亮氨酰-亮氨酰-缬氨酰-酪氨酸-7-氨基-4-甲基香豆素(N-琥珀酰-亮氨酰-亮氨酰-缬氨酰-酪氨酸-AMC)通过体外实验和在完整细胞中测定钙蛋白酶活性,以及通过蛋白质免疫印迹法检测钙蛋白酶特异性血影蛋白降解产物(BDP)。在缺氧7.5分钟时(致死前损伤模型),体外钙蛋白酶活性显著增加(10倍),且不受甘氨酸抑制。在缺氧15分钟时(致死性损伤模型),钙蛋白酶活性进一步增加,但受到甘氨酸抑制。用钙离子载体离子霉素(5 microM)孵育常氧肾小管2分钟和10分钟,钙蛋白酶活性显著增加,且不受甘氨酸抑制。在甘氨酸存在下缺氧15分钟后,近端肾小管的Triton X-100可溶性提取物和胞质提取物中的钙蛋白酶特异性血影蛋白降解产物(BDP)均增加。浓度高达10 mM的甘氨酸对纯化钙蛋白酶的体外钙蛋白酶活性无直接影响。本研究表明:(1)缺氧和离子霉素处理刺激的致死前钙蛋白酶活性增加不受甘氨酸影响;(2)在甘氨酸存在的情况下,缺氧期间钙蛋白酶介导的血影蛋白降解仍会发生;(3)甘氨酸可能通过维持膜对钙内流的完整性来防止致死性损伤后钙蛋白酶活性的进一步增加。