Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, United States.
Elife. 2024 Jul 12;13:e91931. doi: 10.7554/eLife.91931.
Most nervous systems combine both transmitter-mediated and direct cell-cell communication, known as 'chemical' and 'electrical' synapses, respectively. Chemical synapses can be identified by their multiple structural components. Electrical synapses are, on the other hand, generally defined by the presence of a 'gap junction' (a cluster of intercellular channels) between two neuronal processes. However, while gap junctions provide the communicating mechanism, it is unknown whether electrical transmission requires the contribution of additional cellular structures. We investigated this question at identifiable single synaptic contacts on the zebrafish Mauthner cells, at which gap junctions coexist with specializations for neurotransmitter release and where the contact unequivocally defines the anatomical limits of a synapse. Expansion microscopy of these single contacts revealed a detailed map of the incidence and spatial distribution of proteins pertaining to various synaptic structures. Multiple gap junctions of variable size were identified by the presence of their molecular components. Remarkably, most of the synaptic contact's surface was occupied by interleaving gap junctions and components of adherens junctions, suggesting a close functional association between these two structures. In contrast, glutamate receptors were confined to small peripheral portions of the contact, indicating that most of the synaptic area functions as an electrical synapse. Thus, our results revealed the overarching organization of an electrical synapse that operates with not one, but multiple gap junctions, in close association with structural and signaling molecules known to be components of adherens junctions. The relationship between these intercellular structures will aid in establishing the boundaries of electrical synapses found throughout animal connectomes and provide insight into the structural organization and functional diversity of electrical synapses.
大多数神经系统结合了递质介导和直接的细胞间通讯,分别称为“化学”和“电”突触。化学突触可以通过其多个结构成分来识别。另一方面,电突触通常通过两个神经元过程之间存在“缝隙连接”(细胞间通道簇)来定义。然而,虽然缝隙连接提供了通讯机制,但尚不清楚电传递是否需要额外的细胞结构的贡献。我们在斑马鱼 Mauthner 细胞的可识别的单个突触接触处研究了这个问题,在这些突触接触处,缝隙连接与神经递质释放的专门化共存,并且接触明确定义了突触的解剖学界限。对这些单个接触点的扩展显微镜检查揭示了与各种突触结构相关的蛋白质的发生率和空间分布的详细图谱。通过存在其分子成分,可以识别出多个大小不同的缝隙连接。值得注意的是,突触接触的大部分表面被交错的缝隙连接和黏附连接的成分占据,表明这两种结构之间存在紧密的功能关联。相比之下,谷氨酸受体局限于接触的小周边部分,表明大部分突触区域作为电突触发挥作用。因此,我们的结果揭示了一个电突触的总体组织,该突触不仅使用一个缝隙连接,而且还与已知是黏附连接成分的结构和信号分子紧密相关。这些细胞间结构之间的关系将有助于确定整个动物连接组中发现的电突触的边界,并深入了解电突触的结构组织和功能多样性。