Wang A, Barber D, Pfeiffer C J
Department of Biomedical Sciences and Pathobiology, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA.
Arch Environ Contam Toxicol. 2001 Nov;41(4):403-9. doi: 10.1007/s002440010266.
Marine mammals are known for their low susceptibility to mercury toxicity, and selenium may play a role in this protection against mercury intoxication. To gain insight into mechanisms by which selenium might inhibit mercury toxicity in cetacean cells, we investigated the effects of sodium selenite on cell proliferation and cell death (including apoptosis, oncosis, and necrosis) of control and mercuric chloride-treated Atlantic spotted dolphin renal cells (Sp1K cells). Concurrent exposure to 80 microM Na2SeO3 provided full protection against the decrease in cell proliferation induced by 20 microM HgCl2. Pretreatment with Na2SeO3 increased the protective effects of selenium administered later in conjunction with mercury, but pretreatment alone did not provide protection against mercury given alone. Furthermore, Na2SeO3 administered after the exposure to HgCl2 did not protect cells. These data suggest that the coexistence of Na2SeO3 and HgCl2 was essential for the protective effects of Na2SeO3 against the toxicity of HgCl2 in Sp1K cells, and may involve selenium-mercury binding. This is supported by the results of an experiment in which earlier premixed mercury and selenium solutions were less cytotoxic than freshly mixed solutions. Furthermore, HgCl2 induced apoptosis in Sp1K cells, as revealed by nuclear specific dye (7-AAD) incorporation and cell flow cytometry, and this was prevented by the concurrent exposure to Na2SeO3. Inhibition of mercury-induced apoptosis in marine mammal cells, provided by selenium, may contribute to the in vivo protection. This study is the first report that addresses the mechanism of mercury-selenium antagonism in cultured cetacean cells at the cellular level.
海洋哺乳动物以其对汞毒性的低易感性而闻名,硒可能在这种防止汞中毒的保护作用中发挥作用。为了深入了解硒抑制鲸类细胞中汞毒性的机制,我们研究了亚硒酸钠对对照和氯化汞处理的大西洋斑点海豚肾细胞(Sp1K细胞)的细胞增殖和细胞死亡(包括凋亡、胀亡和坏死)的影响。同时暴露于80微摩尔的亚硒酸钠可完全防止20微摩尔氯化汞诱导的细胞增殖减少。用亚硒酸钠预处理可增强随后与汞联合施用的硒的保护作用,但单独预处理并不能防止单独给予汞时的毒性。此外,在暴露于氯化汞后施用亚硒酸钠并不能保护细胞。这些数据表明,亚硒酸钠和氯化汞的共存对于亚硒酸钠对Sp1K细胞中氯化汞毒性的保护作用至关重要,并且可能涉及硒汞结合。这得到了一项实验结果的支持,即早期预混合的汞和硒溶液的细胞毒性低于新鲜混合的溶液。此外,如通过核特异性染料(7-AAD)掺入和细胞流式细胞术所揭示的,氯化汞诱导Sp1K细胞凋亡,而同时暴露于亚硒酸钠可防止这种凋亡。硒对海洋哺乳动物细胞中汞诱导的凋亡的抑制作用可能有助于体内保护。本研究是第一份在细胞水平上探讨培养的鲸类细胞中汞硒拮抗机制的报告。