Lindane (gamma-hexachlorocyclohexane) induces internal Ca2+ release and capacitative Ca2+ entry in Madin-Darby canine kidney cells.

C H Lu, K C Lee, Y C Chen, J S Cheng, M S Yu, W C Chen, C R Jan
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引用次数: 8

Abstract

The effect of lindane (gamma-hexachlorocyclohexane), an organochlorine pesticide, on Ca2+ mobilization in Madin-Darby canine kidney cells was examined by fluorimetry using fura-2 as a Ca2+ indicator. Lindane (5-200 microM) increased [Ca2+]i concentration-dependently. The [Ca2+]i signal comprised an immediate initial rise followed by a persistent phase. Ca2+ removal inhibited the [Ca2+]i signal by reducing both the initial rise and the sustained phase. This implies lindane-triggered Ca2+ influx and Ca2+ release. In Ca2+ -free medium, 0.15 mM lindane increased [Ca2+]i after pretreatment with carbonylcyanide m-chlorophenylhydrazone (CCCP, 2 microM), a mitochondrial uncoupler, and two endoplasmic reticulum Ca2+ pump inhibitors, thapsigargin and cyclopiazonic acid. Conversely, pretreatment with lindane abolished CCCP- and thapsigargin-induced Ca2+ release. This suggests that 0.15 mM lindane released Ca2+ from the endoplasmic reticulum, mitochondria and other stores. La3+ (1 mM) partly inhibited 0.1 mM lindane-induced [Ca2+]i increase, confirming that lindane induced Ca2+ influx. Addition of 3 mM Ca2+ increased [Ca2+]i after pretreatment with 0.15 mM lindane for 750 sec. in Ca2+ -free medium, which indicates lindane-induced capacitative Ca2+ entry. Lindane (0.15 mM)-induced Ca2+ release was not reduced by inhibiting phospholipase C with 2 microM U73122, but was inhibited by 70% by the phospholipase A2 inhibitor aristolochic acid (40 microM).

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林丹(γ -六氯环己烷)诱导Madin-Darby犬肾细胞内Ca2+释放和Ca2+进入。
以呋喃-2作为Ca2+指示剂,采用荧光法研究了有机氯农药林丹(γ -六氯环己烷)对Madin-Darby犬肾细胞Ca2+动员的影响。林丹(5 ~ 200 μ m)使[Ca2+]i浓度升高。[Ca2+]i信号包括一个直接的初始上升,随后是一个持续的阶段。Ca2+去除抑制[Ca2+]i信号通过减少初始上升和持续阶段。这意味着林丹触发Ca2+内流和Ca2+释放。在无Ca2+的培养基中,0.15 mM林丹与2微米的羰基氰化间氯苯腙(CCCP)、线粒体解偶联剂和两种内质网Ca2+泵抑制剂thapsigargin和环吡唑酸预处理后,[Ca2+]i增加。相反,林丹预处理可消除CCCP-和thapsigarin诱导的Ca2+释放。这表明0.15 mM林丹从内质网、线粒体和其他储存中释放Ca2+。La3+ (1 mM)部分抑制0.1 mM林丹诱导的[Ca2+]i增加,证实林丹诱导Ca2+内流。在无Ca2+的培养基中,0.15 mM林丹预处理750秒后,添加3 mM Ca2+增加了[Ca2+]i,这表明林丹诱导了Ca2+的容性进入。2 μ m U73122抑制磷脂酶C对林丹(0.15 mM)诱导的Ca2+释放没有抑制作用,而磷脂酶A2抑制剂马兜铃酸(40 μ m)对林丹(0.15 mM)诱导的Ca2+释放有70%的抑制作用。
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