Klöcker N, Oliver D, Ruppersberg J P, Knaus H G, Fakler B
Department of Physiology II, University of Tübingen, Ob dem Himmelreich 7, Tübingen, 72074, Germany.
Mol Cell Neurosci. 2001 Mar;17(3):514-20. doi: 10.1006/mcne.2000.0956.
Small-conductance Ca(2+)-activated potassium (SK) channels are present in most central neurons, where they mediate the afterhyperpolarizations (AHPs) following action potentials. SK channels integrate changes in intracellular Ca(2+) concentration with membrane potential and thus play an important role in controlling firing pattern and excitability. Here, we characterize the expression pattern of the apamin-sensitive SK subunits, SK2 and SK3, in the developing and adult rat retina using in situ hybridization and immunohistochemistry. The SK2 subunit showed a distinct and developmentally regulated pattern of expression. It appeared during the first postnatal week and located to retinal ganglion cells and to subpopulations of neurons in the inner nuclear layer. These neurons were identified as horizontal cells and dopaminergic amacrine cells by specific markers. In contrast to SK2, the SK3 subunit was detected neither in the developing nor in the adult retina. These results show cell-specific expression of the SK2 subunit in the retina and suggest that this channel underlies the apamin-sensitive AHP currents described in retinal ganglion cells.
小电导钙激活钾(SK)通道存在于大多数中枢神经元中,它们在动作电位后介导超极化后电位(AHPs)。SK通道将细胞内Ca(2+)浓度的变化与膜电位整合在一起,因此在控制放电模式和兴奋性方面发挥着重要作用。在这里,我们使用原位杂交和免疫组织化学方法,对发育中和成年大鼠视网膜中蜂毒明肽敏感的SK亚基SK2和SK3的表达模式进行了表征。SK2亚基表现出独特的、受发育调控的表达模式。它在出生后的第一周出现,并定位于视网膜神经节细胞和内核层中的神经元亚群。通过特异性标记物,这些神经元被鉴定为水平细胞和多巴胺能无长突细胞。与SK2不同,在发育中的视网膜和成年视网膜中均未检测到SK3亚基。这些结果表明SK2亚基在视网膜中具有细胞特异性表达,并提示该通道是视网膜神经节细胞中描述的蜂毒明肽敏感的AHP电流的基础。