Giachello Carlo N G, Hunter Iain, Pettini Tom, Coulson Bramwell, Knüfer Athene, Cachero Sebastian, Winding Michael, Arzan Zarin Aref, Kohsaka Hiroshi, Fan Yuen Ngan, Nose Akinao, Landgraf Matthias, Baines Richard A
Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Manchester Academic Health Science Centre, Manchester M13 9NQ, United Kingdom.
J Neurosci. 2022 Aug 31;42(35):6724-6738. doi: 10.1523/JNEUROSCI.2463-21.2022.
The connectome project aims to map the synaptic connectivity of entire larval and adult fly neural networks, which is essential for understanding nervous system development and function. So far, the project has produced an impressive amount of electron microscopy data that has facilitated reconstructions of specific synapses, including many in the larval locomotor circuit. While this breakthrough represents a technical tour de force, the data remain underutilized, partly because of a lack of functional validation of reconstructions. Attempts to validate connectivity posited by the connectome project, have mostly relied on behavioral assays and/or GFP reconstitution across synaptic partners (GRASP) or GCaMP imaging. While these techniques are useful, they have limited spatial or temporal resolution. Electrophysiological assays of synaptic connectivity overcome these limitations. Here, we combine patch-clamp recordings with optogenetic stimulation in male and female larvae, to test synaptic connectivity proposed by connectome reconstructions. Specifically, we use multiple driver lines to confirm that several connections between premotor interneurons and the anterior corner cell motoneuron are, as the connectome project suggests, monosynaptic. In contrast, our results also show that conclusions based on GRASP imaging may provide false-positive results regarding connectivity between cells. We also present a novel imaging tool, based on the same technology as our electrophysiology, as a favorable alternative to GRASP imaging. Finally, of eight Gal4 lines tested, five are reliably expressed in the premotor interneurons they are targeted to. Thus, our work highlights the need to confirm functional synaptic connectivity, driver line specificity, and use of appropriate genetic tools to support connectome projects. The connectome project aims to provide a complete description of connectivity between neurons in an organism that presents experimental advantages over other models. It has reconstructed hundreds of thousands of synaptic connections of the fly larva by manual identification of anatomic landmarks present in serial section transmission electron microscopy (ssTEM) volumes of the larval CNS. We use a highly reliable electrophysiological approach to verify these connections, providing useful insight into the accuracy of work based on ssTEM. We also present a novel imaging tool for validating excitatory monosynaptic connections between cells and show that several genetic driver lines designed to target neurons of the larval connectome exhibit nonspecific and/or unreliable expression.
连接体项目旨在绘制整个幼虫和成虫果蝇神经网络的突触连接图谱,这对于理解神经系统的发育和功能至关重要。到目前为止,该项目已经产生了大量令人印象深刻的电子显微镜数据,这些数据有助于对特定突触进行重建,包括幼虫运动回路中的许多突触。虽然这一突破代表了一项技术壮举,但这些数据仍未得到充分利用,部分原因是缺乏对重建结果的功能验证。试图验证连接体项目所假定的连接性,大多依赖于行为分析和/或跨突触伙伴的绿色荧光蛋白重建(GRASP)或绿色荧光钙蛋白成像。虽然这些技术很有用,但它们的空间或时间分辨率有限。突触连接性的电生理分析克服了这些局限性。在这里,我们在雄性和雌性幼虫中结合膜片钳记录与光遗传学刺激,以测试连接体重建所提出的突触连接性。具体而言,我们使用多个驱动系来确认,如连接体项目所表明的,运动前中间神经元与前角细胞运动神经元之间的几种连接是单突触的。相比之下,我们的结果还表明,基于GRASP成像得出的结论可能会在细胞间连接性方面提供假阳性结果。我们还提出了一种基于与我们的电生理学相同技术的新型成像工具,作为GRASP成像的一个有利替代方案。最后,在所测试的8个Gal4系中,有5个在它们所靶向的运动前中间神经元中可靠表达。因此,我们的工作强调了确认功能性突触连接性、驱动系特异性以及使用适当的遗传工具来支持连接体项目的必要性。连接体项目旨在提供对生物体中神经元之间连接性的完整描述,该生物体具有优于其他模型的实验优势。它通过手动识别幼虫中枢神经系统连续切片透射电子显微镜(ssTEM)体积中存在的解剖标志,重建了果蝇幼虫的数十万条突触连接。我们使用一种高度可靠的电生理方法来验证这些连接,为基于ssTEM的工作的准确性提供了有用的见解。我们还提出了一种用于验证细胞间兴奋性单突触连接的新型成像工具,并表明几种设计用于靶向幼虫连接体神经元的遗传驱动系表现出非特异性和/或不可靠的表达。