Zhu Shihan, Shen Zeyu, Wu Xiandeng, Zhang Mingjie
School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China; Division of Life Science, Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong, Kowloon, China.
School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China.
Curr Opin Neurobiol. 2025 Feb;90:102975. doi: 10.1016/j.conb.2025.102975. Epub 2025 Feb 1.
A neuronal synapse is formed by juxtaposition of a transmitter releasing presynaptic bouton of one neuron with a transmitter receiving postsynaptic compartment such as a spine protrusion of another neuron. Each presynaptic bouton and postsynaptic spine, though very small in their volumes already, are further compartmentalized to micro-/nano-domains with distinct molecular organizations and synaptic functions. This review summarizes studies in recent years demonstrating that multivalent protein-protein interaction-induced phase separation underlies formation and coexistence of multiple distinct molecular condensates within tiny synapses. In post-synapses where synaptic compartmentalization via phase separation was first demonstrated, phase separation allows clustering of transmitter receptors into distinct nanodomains and renders postsynaptic densities to be regulated by synaptic stimulation signals for plasticity. In pre-synapses, such phase separation-mediated synaptic condensates formation allows SVs to be stored as distinct pools and directly transported for activity-induced transmitter release.
神经元突触是由一个神经元释放递质的突触前终扣与另一个神经元接收递质的突触后区室(如棘突)并列形成的。每个突触前终扣和突触后棘突,尽管其体积已经非常小,但进一步被划分为具有不同分子组织和突触功能的微/纳米域。本综述总结了近年来的研究,这些研究表明多价蛋白质-蛋白质相互作用诱导的相分离是微小突触内多种不同分子凝聚物形成和共存的基础。在首次证明通过相分离进行突触区室化的突触后部位,相分离允许递质受体聚集到不同的纳米域,并使突触后致密物受突触刺激信号调节以实现可塑性。在突触前部位,这种相分离介导的突触凝聚物形成允许突触小泡作为不同的池储存,并直接运输以进行活动诱导的递质释放。