TRI-NORMAL-BUTYLTIN INCREASES INTRACELLULAR CA2+ IN MOUSE THYMOCYTES - A FLOW-CYTOMETRIC STUDY USING FLUORESCENT DYES FOR MEMBRANE-POTENTIAL AND INTRACELLULAR CA2+

Effects of tri-n-butyltin (TBT) on mouse thymocytes were examined using a flow-cytometer and fluorescent dyes for membrane potential and intracellular Ca2+ ([Ca2+]i). TBT at concentrations from 1 x 10(-7) M to 3 x 10(-7) M caused hyperpolarization in thymocytes during 30 min. after drug application in a time- and dose-dependent manner. Further increase in TBT concentration (to 1 x 10(-6) M) made hyperpolarization of thymocytes more profound within 5 min. after application. thereafter gradually depolarized them during the next 25 min. TBT at 3 x 10(-8) M or more (up to 1 x 10(-6) M) increased the [Ca2+]i of thymocytes. After reaching maximum [Ca2+]i at the various TBT concentrations used within 5 min. after drug application, the [Ca2+]i slightly decreased in a time-dependent manner. Effects of TBT on membrane potential and the [Ca2+]i were greatly reduced under nominal external Ca2+-free condition. Results suggest that TBT can promote Ca2+-influx to thymocytes, resulting in hyperpolarization by activation of Ca2+-dependent K+ current. The increase in [Ca2+]i by TBT may be related to its cytotoxic action on thymocytes.