Yasuo Oyama, David O. Carpenter , Shinya Ueno , Hiromi Hayashi, Fukiyo Tomiyoshi
{"title":"甲基汞诱导小鼠胸腺细胞Ca2+依赖性超极化:使用荧光染料的流式细胞术研究","authors":"Yasuo Oyama, David O. Carpenter , Shinya Ueno , Hiromi Hayashi, Fukiyo Tomiyoshi","doi":"10.1016/0926-6917(95)00003-8","DOIUrl":null,"url":null,"abstract":"<div><p>The effect of methylmercury on mouse thymocytes was examined using fluorescent dyes for membrane potential and intracellular Ca<sup>2+</sup>. Methylmercury at concentrations of 1 ωM or higher (up to 30 ωM) produced hyperpolarization in a dose-dependent fashion. Charybdotoxin and quinine, but not 4-aminopyridine and tetraethylammonium, greatly suppressed methylmercury-induced hyperpolarization. Removal of external Ca<sup>2+</sup> reduced the degree of hyperpolarization. Pretreatment of thymocytes with A23187 under Ca<sup>2+</sup>-free conditions abolished the hyperpolarization induced by methylmercury. Under both normal and Ca<sup>2+</sup>-free conditions methylmercury increased the intracellular concentration of Ca<sup>2+</sup>. The results suggest that the increase in intracellular Ca<sup>2+</sup> is mediated through a Ca<sup>2+</sup> release from intracellular stores as well as through influx of external Ca<sup>2+</sup>. Therefore, it is likely that methylmercury increases the intracellular concentration of Ca<sup>2+</sup>, resulting in activation of Ca<sup>2+</sup>-dependent K<sup>+</sup> conductance of mouse thymocytes.</p></div>","PeriodicalId":100501,"journal":{"name":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","volume":"293 2","pages":"Pages 101-107"},"PeriodicalIF":0.0000,"publicationDate":"1995-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6917(95)00003-8","citationCount":"25","resultStr":"{\"title\":\"Methylmercury induces Ca2+-dependent hyperpolarization of mouse thymocytes: a flow cytometric study using fluorescent dyes\",\"authors\":\"Yasuo Oyama, David O. Carpenter , Shinya Ueno , Hiromi Hayashi, Fukiyo Tomiyoshi\",\"doi\":\"10.1016/0926-6917(95)00003-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The effect of methylmercury on mouse thymocytes was examined using fluorescent dyes for membrane potential and intracellular Ca<sup>2+</sup>. Methylmercury at concentrations of 1 ωM or higher (up to 30 ωM) produced hyperpolarization in a dose-dependent fashion. Charybdotoxin and quinine, but not 4-aminopyridine and tetraethylammonium, greatly suppressed methylmercury-induced hyperpolarization. Removal of external Ca<sup>2+</sup> reduced the degree of hyperpolarization. Pretreatment of thymocytes with A23187 under Ca<sup>2+</sup>-free conditions abolished the hyperpolarization induced by methylmercury. Under both normal and Ca<sup>2+</sup>-free conditions methylmercury increased the intracellular concentration of Ca<sup>2+</sup>. The results suggest that the increase in intracellular Ca<sup>2+</sup> is mediated through a Ca<sup>2+</sup> release from intracellular stores as well as through influx of external Ca<sup>2+</sup>. Therefore, it is likely that methylmercury increases the intracellular concentration of Ca<sup>2+</sup>, resulting in activation of Ca<sup>2+</sup>-dependent K<sup>+</sup> conductance of mouse thymocytes.</p></div>\",\"PeriodicalId\":100501,\"journal\":{\"name\":\"European Journal of Pharmacology: Environmental Toxicology and Pharmacology\",\"volume\":\"293 2\",\"pages\":\"Pages 101-107\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1995-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0926-6917(95)00003-8\",\"citationCount\":\"25\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Pharmacology: Environmental Toxicology and Pharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0926691795000038\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0926691795000038","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Methylmercury induces Ca2+-dependent hyperpolarization of mouse thymocytes: a flow cytometric study using fluorescent dyes
The effect of methylmercury on mouse thymocytes was examined using fluorescent dyes for membrane potential and intracellular Ca2+. Methylmercury at concentrations of 1 ωM or higher (up to 30 ωM) produced hyperpolarization in a dose-dependent fashion. Charybdotoxin and quinine, but not 4-aminopyridine and tetraethylammonium, greatly suppressed methylmercury-induced hyperpolarization. Removal of external Ca2+ reduced the degree of hyperpolarization. Pretreatment of thymocytes with A23187 under Ca2+-free conditions abolished the hyperpolarization induced by methylmercury. Under both normal and Ca2+-free conditions methylmercury increased the intracellular concentration of Ca2+. The results suggest that the increase in intracellular Ca2+ is mediated through a Ca2+ release from intracellular stores as well as through influx of external Ca2+. Therefore, it is likely that methylmercury increases the intracellular concentration of Ca2+, resulting in activation of Ca2+-dependent K+ conductance of mouse thymocytes.