Grosse G, Draguhn A, Höhne L, Tapp R, Veh R W, Ahnert-Hilger G
Institut für Anatomie der Charité, Humboldt-Universität zu Berlin, 10115 Berlin, Germany.
J Neurosci. 2000 Mar 1;20(5):1869-82. doi: 10.1523/JNEUROSCI.20-05-01869.2000.
Excitability and discharge behavior of neurons depends on the highly variable expression pattern of voltage-dependent potassium (Kv) channels throughout the nervous system. To learn more about distribution, development, and activity-dependent regulation of Kv channel subunit expression in the rodent hippocampus, we studied the protein expression of members of the Kv1 subfamily in mouse hippocampus in situ and in primary cultures. In adult hippocampus, Kv1 (1-6) channel alpha-subunits were present, whereas at postnatal day 2, none of these proteins could be detected in CA1-CA3 and dentate gyrus. Kv1.1 was the first channel to be observed at postnatal day 6. The delayed postnatal expression and most of the subcellular distribution observed in hippocampal sections were mimicked by cultured hippocampal neurons in which Kv channels appeared only after 10 days in vitro. This developmental upregulation was paralleled by a dramatic increase in total K(+) current, as well as an elevated GABA release in the presence of 4-aminopyridine. Thus, the developmental profile, subcellular localization, and functionality of Kv1 channels in primary culture of hippocampus closely resembles the in situ situation. Impairing secretion by clostridial neurotoxins or blocking activity by tetrodotoxin inhibited the expression of Kv1.1, Kv1.2, and Kv1.4, whereas the other Kv1 channels still appeared. This activity-dependent depression was only observed before the initial appearance of the respective channels and lost after they had been expressed. Our data show that hippocampal neurons in culture are a convenient model to study the developmental expression and regulation of Kv1 channels. The ontogenetic regulation and the activity-dependent expression of Kv1.1, Kv1.2, and Kv1.4 indicate that neuronal activity plays a crucial role for the development of the mature Kv channel pattern in hippocampal neurons.
神经元的兴奋性和放电行为取决于整个神经系统中电压依赖性钾(Kv)通道高度可变的表达模式。为了更多地了解啮齿动物海马体中Kv通道亚基表达的分布、发育以及活动依赖性调节,我们研究了Kv1亚家族成员在小鼠海马体原位和原代培养物中的蛋白质表达。在成年海马体中,存在Kv1(1 - 6)通道α亚基,而在出生后第2天,在CA1 - CA3和齿状回中未检测到这些蛋白质中的任何一种。Kv1.1是在出生后第6天首次观察到的通道。培养的海马神经元模拟了海马切片中观察到的出生后延迟表达和大部分亚细胞分布,其中Kv通道仅在体外培养10天后才出现。这种发育上调与总钾离子电流的显著增加以及在4 - 氨基吡啶存在下GABA释放的升高并行。因此,海马体原代培养物中Kv1通道的发育概况、亚细胞定位和功能与原位情况非常相似。肉毒杆菌神经毒素损害分泌或河豚毒素阻断活动会抑制Kv1.1、Kv1.2和Kv1.4的表达,而其他Kv1通道仍然出现。这种活动依赖性抑制仅在相应通道最初出现之前观察到,在它们表达后消失。我们的数据表明,培养的海马神经元是研究Kv1通道发育表达和调节的便捷模型。Kv1.1、Kv1.2和Kv1.4的个体发生调节和活动依赖性表达表明,神经元活动在海马神经元成熟Kv通道模式的发育中起着关键作用。