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Evidence of elevated intracellular calcium levels in weaver homozygote mice

机译:织布纯合子小鼠细胞内钙水平升高的证据

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class="enumerated" style="list-style-type:decimal">A mutation in the G-protein-linked, inwardly rectifying K+ channel GIRK2 leads to the loss of cerebellar and dopaminergic mesencephalic neurons in weaver mice. The steps leading to cell death are not well understood but may involve constitutive influx of Na+ and Ca2+ into the neurons.We found that resting [Ca2+]i was dramatically higher in cerebellar neurons from weaver mice compared to wild-type neurons.High-K+ stimuli elicited much smaller changes in [Ca2+]i in weaver cerebellar neurons compared to wild-type neurons.weaver cerebellar granule cells could be rescued from cell death by the GIRK2wv cationic channel blocker, QX-314.QX-314 lowered resting intracellular Ca2+ levels in weaver cerebellar granule cells.These results suggest that changes in resting [Ca2+]i levels and alterations in K+ channel function are most likely to contribute to the developmental abnormalities and increased cerebellar cell death observed in weaver mice.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 与G蛋白连接的,向内整流的K + 通道GIRK2的突变导致织布工小鼠的小脑和多巴胺能中脑神经元丢失。导致细胞死亡的步骤尚不清楚,但可能涉及Na + 和Ca 2 + 组成性地流入神经元。 我们发现与野生型神经元相比,Weaver小鼠小脑神经元的静止[Ca 2 + ] i显着更高。 高K + 刺激引起与野生型神经元相比,韦弗小脑神经元中[Ca 2 + ] i的变化要小得多。 韦弗小脑颗粒细胞可以通过GIRK2wv阳离子通道从细胞死亡中拯救出来阻滞剂QX-314。 Qli-QX-314降低了韦弗小脑颗粒细胞中静息细胞内Ca 2 + 的水平。 这些结果表明静息状态的变化[Ca 2 + ] i水平和K + 通道功能的改变最有可能导致织布工小鼠发育异常和小脑细胞死亡增加。

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