CNRS, INP UMR7051, NeuroCyto, Aix Marseille Université , Marseille, France.
Abbelight , Cachan, France.
J Cell Biol. 2023 Oct 2;222(10). doi: 10.1083/jcb.202208110. Epub 2023 Aug 14.
The architecture of the actin cytoskeleton that concentrates at presynapses remains poorly known, hindering our understanding of its roles in synaptic physiology. In this work, we measure and visualize presynaptic actin by diffraction-limited and super-resolution microscopy, thanks to a validated model of bead-induced presynapses in cultured neurons. We identify a major population of actin-enriched presynapses that concentrates more presynaptic components and shows higher synaptic vesicle cycling than their non-enriched counterparts. Pharmacological perturbations point to an optimal actin amount and the presence of distinct actin structures within presynapses. We directly visualize these nanostructures using Single Molecule Localization Microscopy (SMLM), defining three distinct types: an actin mesh at the active zone, actin rails between the active zone and deeper reserve pools, and actin corrals around the whole presynaptic compartment. Finally, CRISPR-tagging of endogenous actin allows us to validate our results in natural synapses between cultured neurons, confirming the role of actin enrichment and the presence of three types of presynaptic actin nanostructures.
集中在突触前的肌动蛋白细胞骨架结构仍知之甚少,这阻碍了我们对其在突触生理学中作用的理解。在这项工作中,我们通过衍射限制和超分辨率显微镜来测量和可视化突触前肌动蛋白,这要归功于在培养神经元中经验证的珠诱导突触前模型。我们确定了一个主要的富含肌动蛋白的突触前群体,该群体集中了更多的突触前成分,并显示出比非富集物更高的突触小泡循环。药理干扰表明存在最佳肌动蛋白数量和不同的肌动蛋白结构。我们使用单分子定位显微镜(SMLM)直接可视化这些纳米结构,定义了三种不同的类型:活性区的肌动蛋白网格、活性区和更深的储备池之间的肌动蛋白轨道,以及整个突触前区周围的肌动蛋白围栏。最后,通过 CRISPR 标记内源性肌动蛋白,我们可以在培养神经元之间的自然突触中验证我们的结果,证实了肌动蛋白富集的作用和三种类型的突触前肌动蛋白纳米结构的存在。