University of Leicester, Department of Neuroscience, Psychology and Behaviour, University Road, Leicester LE1 7RH, United Kingdom
University of Leicester, Department of Neuroscience, Psychology and Behaviour, University Road, Leicester LE1 7RH, United Kingdom.
J Neurosci. 2018 Apr 11;38(15):3741-3752. doi: 10.1523/JNEUROSCI.2310-17.2018. Epub 2018 Mar 14.
Insect auditory receivers provide an excellent comparative resource to understand general principles of auditory transduction, but analysis of the electrophysiological properties of the auditory neurons has been hampered by their tiny size and inaccessibility. Here we pioneer patch-clamp recordings from the auditory neurons of Müller's organ of the desert locust to characterize dendritic spikes, axonal spikes, and the transduction current. We demonstrate that dendritic spikes, elicited by sound stimuli, trigger axonal spikes, and that both types are sodium and voltage dependent and blocked by TTX. Spontaneous discrete depolarizations summate upon acoustic stimulation to produce a graded transduction potential that in turn elicits the dendritic spikes. The transduction current of Group III neurons of Müller's organ, which are broadly tuned to 3 kHz, is blocked by three ion channel blockers (FM1-43, streptomycin, and 2-APB) that are known to block mechanotransduction channels. We investigated the contribution of the candidate mechanotransduction ion channel Nanchung-Inactive-which is expressed in Müller's organ-to the transduction current. A specific agonist of Nanchung-Inactive, pymetrozine, eliminates the sound-evoked transduction current while inducing a tonic depolarizing current of comparable amplitude. The Nanchung-Inactive ion channels, therefore, have the required conductance to carry the entire transduction current, and sound stimulation appears not to open any additional channels. The application of three mechanotransduction ion channel blockers prevented the pymetrozine-induced depolarizing current. This implies that either Nanchung-Inactive is, or forms part of, the mechanotransduction ion channel or it amplifies a relatively small current (<30 pA) produced by another mechanotransduction ion channel such as NompC. The mechanically activated ion channel underpinning hearing is not known. We have pioneered intracellular patch-clamp recordings from locust auditory neurons to unravel the role of the candidate mechanotransduction ion channel Nanchung-Inactive in auditory transduction in insects.
昆虫听觉接收器为理解听觉转导的一般原理提供了极好的比较资源,但由于其体积小且难以接近,因此对听觉神经元的电生理特性的分析一直受到阻碍。在这里,我们率先从沙漠蝗 Müller 器的听觉神经元进行膜片钳记录,以表征树突棘、轴突棘和转导电流。我们证明,由声音刺激引发的树突棘会引发轴突棘,并且这两种类型都是钠依赖性和电压依赖性的,并被 TTX 阻断。自发离散去极化在声刺激下累积,产生分级转导电位,进而引发树突棘。对广泛调谐到 3 kHz 的 Müller 器第三组神经元的转导电流被三种离子通道阻断剂(FM1-43、链霉素和 2-APB)阻断,这些阻断剂已知可阻断机械转导通道。我们研究了候选机械转导离子通道 Nanchung-Inactive 的贡献-Nanchung-Inactive 在 Müller 器中表达-对转导电流的贡献。Nanchung-Inactive 的一种特异性激动剂吡虫啉消除了声音诱发的转导电流,同时诱导了幅度相当的持续去极化电流。因此,Nanchung-Inactive 离子通道具有携带整个转导电流的所需电导,并且声音刺激似乎不会打开任何其他通道。三种机械转导离子通道阻断剂的应用阻止了吡虫啉诱导的去极化电流。这意味着 Nanchung-Inactive 要么是,要么是机械转导离子通道的一部分,要么它放大了另一种机械转导离子通道(如 NompC)产生的相对较小的电流(<30 pA)。产生听觉的机械激活离子通道尚不清楚。我们率先从蝗虫听觉神经元进行细胞内膜片钳记录,以揭示候选机械转导离子通道 Nanchung-Inactive 在昆虫听觉转导中的作用。