Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030.
Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, Texas 77030.
J Neurosci. 2020 Oct 14;40(42):7999-8024. doi: 10.1523/JNEUROSCI.0142-20.2020. Epub 2020 Sep 14.
In multipolar vertebrate neurons, action potentials (APs) initiate close to the soma, at the axonal initial segment. Invertebrate neurons are typically unipolar with dendrites integrating directly into the axon. Where APs are initiated in the axons of invertebrate neurons is unclear. Voltage-gated sodium (Na) channels are a functional hallmark of the axonal initial segment in vertebrates. We used an intronic -Mediated Integration Cassette to determine the endogenous gene expression and subcellular localization of the sole Na channel in both male and female , Despite being the only Na channel in the fly, we show that only 23 ± 1% of neurons in the embryonic and larval CNS express , while in the adult CNS is broadly expressed. We generated a single-cell transcriptomic atlas of the whole third instar larval brain to identify expressing neurons and show that it positively correlates with markers of differentiated, actively firing neurons. Therefore, only 23 ± 1% of larval neurons may be capable of firing Na-dependent APs. We then show that Para is enriched in an axonal segment, distal to the site of dendritic integration into the axon, which we named the distal axonal segment (DAS). The DAS is present in multiple neuron classes in both the third instar larval and adult CNS. Whole cell patch clamp electrophysiological recordings of adult CNS fly neurons are consistent with the interpretation that Na-dependent APs originate in the DAS. Identification of the distal Na localization in fly neurons will enable more accurate interpretation of electrophysiological recordings in invertebrates. The site of action potential (AP) initiation in invertebrates is unknown. We tagged the sole voltage-gated sodium (Na) channel in the fly, , and identified that Para is enriched at a distal axonal segment. The distal axonal segment is located distal to where dendrites impinge on axons and is the likely site of AP initiation. Understanding where APs are initiated improves our ability to model neuronal activity and our interpretation of electrophysiological data. Additionally, is only expressed in 23 ± 1% of third instar larval neurons but is broadly expressed in adults. Single-cell RNA sequencing of the third instar larval brain shows that expression correlates with the expression of active, differentiated neuronal markers. Therefore, only 23 ± 1% of third instar larval neurons may be able to actively fire Na-dependent APs.
在多极脊椎动物神经元中,动作电位 (AP) 起始于靠近胞体的轴突起始段。无脊椎动物神经元通常为单极神经元,树突直接整合到轴突中。无脊椎动物神经元的 AP 起始位置尚不清楚。电压门控钠 (Na) 通道是脊椎动物轴突起始段的功能标志。我们使用内含子介导的整合盒来确定雌雄两性中唯一的 Na 通道的内源性基因表达和亚细胞定位。尽管 是果蝇中的唯一 Na 通道,但我们发现只有 23 ± 1%的胚胎和幼虫中枢神经系统中的神经元表达 ,而在成年中枢神经系统中则广泛表达。我们生成了整个三龄幼虫脑的单细胞转录组图谱,以鉴定表达 的神经元,并表明它与分化的、活跃放电神经元的标志物呈正相关。因此,只有 23 ± 1%的幼虫神经元可能能够产生依赖 Na 的 AP。然后,我们发现 Para 在轴突的一个段中富集,该段位于树突整合到轴突的部位远端,我们将其命名为远端轴突段 (DAS)。在三龄幼虫和成年中枢神经系统中的多个神经元中都存在 DAS。成年中枢神经系统果蝇神经元的全细胞膜片钳电生理记录与以下解释一致,即依赖 Na 的 AP 起源于 DAS。在果蝇神经元中鉴定出远端 Na 定位将使我们能够更准确地解释无脊椎动物的电生理记录。无脊椎动物中 AP 起始位置未知。我们标记了果蝇中唯一的电压门控 Na 通道 ,并确定 Para 在远端轴突段中富集。远端轴突段位于树突与轴突碰撞的部位远端,是 AP 起始的可能部位。了解 AP 的起始位置可以提高我们模拟神经元活动的能力,并改善我们对电生理数据的解释。此外, 仅在 23 ± 1%的三龄幼虫神经元中表达,但在成年期广泛表达。三龄幼虫脑的单细胞 RNA 测序显示, 表达与活跃分化的神经元标志物的表达相关。因此,只有 23 ± 1%的三龄幼虫神经元可能能够主动产生依赖 Na 的 AP。