Shohayeb Belal, Sempert Kai, Wallis Tristan P, Meunier Frédéric A, Durisic Nela, O'Brien Elizabeth A, Flores Cecilia, Cooper Helen M
Queensland Brain Institute, The University of Queensland, Brisbane, QLD 4072, Australia.
Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, Brisbane, QLD 4072, Australia.
iScience. 2024 Jul 30;27(9):110621. doi: 10.1016/j.isci.2024.110621. eCollection 2024 Sep 20.
Synaptic structural plasticity, the expansion of dendritic spines in response to synaptic stimulation, is essential for experience-dependent plasticity and is driven by branched actin polymerization. The WAVE regulatory complex (WRC) is confined to nanodomains at the postsynaptic membrane where it catalyzes actin polymerization. As the netrin/RGM receptor Neogenin is a critical regulator of the WRC, its nanoscale organization may be an important determinant of WRC nanoarchitecture and function. Using super-resolution microscopy, we reveal that Neogenin is highly organized on the spine membrane at the nanoscale level. We show that Neogenin binding to the WRC promotes co-clustering into nanodomains in response to brain-derived neurotrophic factor (BDNF), indicating that nanoclustering occurs in response to synaptic stimulation. Disruption of Neogenin/WRC binding not only prevents BDNF-mediated actin remodeling but also inhibits BDNF-induced calcium signaling. We conclude that the assembly of Neogenin/WRC nanodomains is a prerequisite for BDNF-mediated structural and synaptic plasticity.
突触结构可塑性,即树突棘响应突触刺激而扩张,对于依赖经验的可塑性至关重要,且由分支肌动蛋白聚合驱动。WAVE调节复合体(WRC)局限于突触后膜的纳米域,在那里它催化肌动蛋白聚合。由于网蛋白/RGM受体新生蛋白是WRC的关键调节因子,其纳米级组织可能是WRC纳米结构和功能的重要决定因素。利用超分辨率显微镜,我们揭示新生蛋白在纳米尺度上在棘突膜上高度有序排列。我们表明,新生蛋白与WRC结合会促进其响应脑源性神经营养因子(BDNF)共同聚集形成纳米域,这表明纳米聚集是对突触刺激的响应。破坏新生蛋白/WRC结合不仅会阻止BDNF介导的肌动蛋白重塑,还会抑制BDNF诱导的钙信号传导。我们得出结论,新生蛋白/WRC纳米域的组装是BDNF介导的结构和突触可塑性的先决条件。