首页> 外文期刊>Brain research >Increase of Kv3.1b expression in avian auditory brainstem neurons correlates with synaptogenesis in vivo and in vitro.
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Increase of Kv3.1b expression in avian auditory brainstem neurons correlates with synaptogenesis in vivo and in vitro.

机译:禽听性脑干神经元中Kv3.1b表达的增加与体内外的突触发生有关。

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In the auditory system voltage-activated currents mediated by potassium channels Kv1.1 and Kv3.1b and their interaction with sodium inward currents play a crucial role for computational function. However, it is unresolved how these potassium channels are developmentally regulated. We have therefore combined a biochemical investigation of Kv1.1 and Kv3.1b protein expression with electrophysiological recordings of membrane currents to characterize neuronal differentiation in the auditory brain stem of the chick. Differentiation in vitro was compared with cells prepared from corresponding embryonic stages in vivo. Using a computer model based on the empirical data we were then able to predict physiological properties of developing auditory brain stem neurons. In vivo Kv3.1b expression increased strongly between E10 and E14, a time of functional synaptogenesis in the auditory brainstem. We also found this increase of expression in vitro, again coinciding with synaptogenesis in the cultures. Whole-cell patch recordings revealed a corresponding increase of the (Kv3.1-like) high threshold potassium current. In contrast, Kv1.1 protein expression failed to increase in vitro, and changes in (Kv1.1-like) low threshold potassium current with time in culture were not significant. Electrophysiological recordings revealed that sodium inward currents increased with cultivation time. Thus, our data suggest that Kv3.1b expression occurs with the onset of functional synaptogenesis, while a different signal, absent from cultures of dissociated auditory brain stem, is needed for Kv1.1 expression. A biophysical model constructed with parameters from our recordings was used to investigate the functional impact of the currents mediated by these channels. We found that during development both high and low threshold potassium currents need to be increased in a concerted manner with the sodium conductance for the neurons to exhibit fast and phasic action potential firing and a narrow time window of coincidence detection.
机译:在听觉系统中,钾离子通道Kv1.1和Kv3.1b介导的电压激活电流及其与钠内向电流的相互作用对计算功能起着至关重要的作用。然而,如何调节这些钾离子通道尚待解决。因此,我们将Kv1.1和Kv3.1b蛋白表达的生化研究与膜电流的电生理记录相结合,以表征雏鸡听觉脑干中的神经元分化。将体外分化与从体内相应胚胎阶段制备的细胞进行了比较。然后,使用基于经验数据的计算机模型,我们能够预测发育中的听觉脑干神经元的生理特性。体内Kv3.1b表达在E10和E14(听觉脑干功能性突触发生的时间)之间强烈增加。我们还发现体外表达的这种增加,再次与文化中的突触发生相吻合。全细胞膜片记录显示(Kv3.1-like)高阈值钾电流相应增加。相反,Kv1.1蛋白表达未能在体外增加,并且(Kv1.1-样)低阈值钾电流随培养时间的变化并不显着。电生理记录表明,钠的内流随着培养时间的增加而增加。因此,我们的数据表明Kv3.1b表达的发生与功能性突触的发生有关,而Kv1.1表达需要分离的听觉脑干培养物中不存在的不同信号。用我们的记录中的参数构建的生物物理模型用于研究这些通道介导的电流的功能影响。我们发现,在发育过程中,高阈值钾电流和低阈值钾电流都需要与钠电导以协调的方式增加,以使神经元表现出快速和阶段性的动作电位触发以及同时检测的狭窄时间窗口。

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