Department of Chemistry, Graduate School of Science, Kyoto University, Japan.
Department of Molecular Neuroscience, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Japan.
FEBS J. 2021 Dec;288(24):6913-6926. doi: 10.1111/febs.15666. Epub 2020 Dec 21.
Neurons establish circuits for brain functions such as cognition, emotion, learning, and memory. Their connections are mediated by synapses, which are specialized cell-cell adhesions responsible for neuronal signal transmission. During neurodevelopment, synapse formation is triggered by interactions of cell adhesion molecules termed synaptic organizers or synapse organizers. Type IIa receptor protein tyrosine phosphatases (IIa RPTPs; also known as leukocyte common antigen-related receptor tyrosine phosphatases or LAR-RPTPs) play important roles in axon guidance and neurite extension, and also serve as presynaptic organizers. IIa RPTPs transsynaptically interact with multiple sets of postsynaptic organizers, mostly in a splicing-dependent fashion. Here, we review and update research progress on IIa RPTPs, particularly regarding their functional roles in vivo demonstrated using conditional knockout approach and structural insights into their extracellular and intracellular molecular interactions revealed by crystallography and other biophysical techniques. Future directions in the research field of IIa RPTPs are also discussed, including recent findings of the molecular assembly mechanism underlying the formation of synapse-specific nanostructures essential for synaptic functions.
神经元建立大脑功能的回路,如认知、情感、学习和记忆。它们的连接由突触介导,突触是专门的细胞-细胞黏附物,负责神经元信号传递。在神经发育过程中,突触的形成是由细胞黏附分子相互作用触发的,这些分子被称为突触组织者或突触形成器。IIa 型受体蛋白酪氨酸磷酸酶(IIa RPTPs;也称为白细胞共同抗原相关受体酪氨酸磷酸酶或 LAR-RPTPs)在轴突导向和神经突延伸中发挥重要作用,并且还作为突触前组织者。IIa RPTPs 与多组突触后组织者进行跨突触相互作用,主要以剪接依赖的方式进行。在这里,我们综述和更新了关于 IIa RPTPs 的研究进展,特别是使用条件性敲除方法在体内证明其功能作用,以及通过晶体学和其他生物物理技术揭示其细胞外和细胞内分子相互作用的结构见解。还讨论了 IIa RPTPs 研究领域的未来方向,包括最近发现的形成突触特异性纳米结构的分子组装机制,这些结构对于突触功能至关重要。