The Key Laboratory of Neural and Vascular Biology, Ministry of Education, Hebei Medical University, Shijiazhuang, China 050017.
J Neurosci. 2012 Nov 14;32(46):16314-30. doi: 10.1523/JNEUROSCI.2097-12.2012.
Whereas prehearing spiral ganglion neurons (SGNs) rely faithfully on outputs from spontaneously active developing hair cells, the electrical phenotypes of posthearing neurons are shaped by distinct rapid and graded receptor potentials from hair cells. To date, technical difficulties in isolation of fragile posthearing neurons from the rigid bony labyrinth of the inner ear have hindered analyses of the electrical phenotype of SGNs. Therefore, we have recently developed new strategies to isolate posthearing mouse SGNs for functional analyses. Here, we describe the coarse and fine properties of Ca(2+) currents, which sculpt the firing properties of posthearing SGNs. Murine SGNs express multiple Ca(2+) channel currents to enable diverse functions. We have demonstrated that suppression of Ca(2+) currents results in significant hyperpolarization of the resting membrane potential (rmp) of basal SGNs, suggesting that Ca(2+) influx primes rmp for excitation. In contrast, removal of external Ca(2+) has modest effects on rmp of apical SGNs. The blockade of Ca(2+) currents with a mixture of specific blockers attenuates spontaneously active SGNs. Paradoxically, different subtypes of Ca(2+) currents, such as R-type currents, may activate resting outward conductances since blockage of the current results in depolarization of rmp. In keeping with whole-cell current data, single-channel records revealed multiple diverse Ca(2+) channels in SGNs. Additionally, there were differential expressions of distinct Ca(2+) current densities in the apicobasal contour of the adult cochlea. This report provides invaluable insights into Ca(2+)-dependent processes in adult SGNs.
尽管术前螺旋神经节神经元 (SGN) 依赖于自发活跃发育的毛细胞的输出,但术后神经元的电生理表型是由毛细胞产生的独特快速和分级受体电位塑造的。迄今为止,从内耳刚性骨迷路中分离脆弱的术后神经元的技术困难阻碍了 SGN 电生理表型的分析。因此,我们最近开发了从内耳刚性骨迷路中分离术后小鼠 SGN 的新策略,以进行功能分析。在这里,我们描述了 Ca(2+)电流的粗糙和精细特性,这些特性塑造了术后 SGN 的放电特性。鼠 SGN 表达多种 Ca(2+)通道电流以实现多种功能。我们已经证明,抑制 Ca(2+)电流会导致基础 SGN 的静息膜电位 (rmp) 显著超极化,表明 Ca(2+)内流为兴奋准备 rmp。相比之下,去除外 Ca(2+)对顶 SGN 的 rmp 影响不大。用特定的阻断剂混合物阻断 Ca(2+)电流会减弱自发活跃的 SGN。矛盾的是,不同类型的 Ca(2+)电流,如 R 型电流,可能会激活静止的外向电导,因为阻断电流会导致 rmp 去极化。与全细胞电流数据一致,单通道记录显示 SGN 中有多种不同的 Ca(2+)通道。此外,在成年耳蜗的顶底轮廓中,存在不同的 Ca(2+)电流密度的差异表达。本报告为成年 SGN 中 Ca(2+)依赖性过程提供了宝贵的见解。