Synapse Development and Plasticity Research Unit, Institut de Recherches Cliniques de Montréal (IRCM), Montreal, QC, H2W 1R7, Canada.
Department of Molecular Biology, Faculty of Medicine, Université de Montréal, Montreal, QC, H3T 1J4, Canada.
EMBO J. 2024 Nov;43(22):5690-5717. doi: 10.1038/s44318-024-00252-9. Epub 2024 Sep 27.
The precise organization of pre- and postsynaptic terminals is crucial for normal synaptic function in the brain. In addition to its canonical role as a neurotrophin-3 receptor tyrosine kinase, postsynaptic TrkC promotes excitatory synapse organization through interaction with presynaptic receptor-type tyrosine phosphatase PTPσ. To isolate the synaptic organizer function of TrkC from its role as a neurotrophin-3 receptor, we generated mice carrying TrkC point mutations that selectively abolish PTPσ binding. The excitatory synapses in mutant mice had abnormal synaptic vesicle clustering and postsynaptic density elongation, more silent synapses, and fewer active synapses, which additionally exhibited enhanced basal transmission with impaired release probability. Alongside these phenotypes, we observed aberrant synaptic protein phosphorylation, but no differences in the neurotrophin signaling pathway. Consistent with reports linking these aberrantly phosphorylated proteins to neuropsychiatric disorders, mutant TrkC knock-in mice displayed impaired social responses and increased avoidance behavior. Thus, through its regulation of synaptic protein phosphorylation, the TrkC-PTPσ complex is crucial for the maturation, but not formation, of excitatory synapses in vivo.
神经递质-3 受体酪氨酸激酶 TrkC 通过与突触前受体型酪氨酸磷酸酶 PTPσ 相互作用,促进兴奋性突触的组织,除了其作为神经营养因子-3 受体的典型作用之外。为了从神经营养因子-3 受体的作用中分离出 TrkC 的突触组织者功能,我们生成了携带选择性消除 PTPσ 结合的 TrkC 点突变的小鼠。突变小鼠的兴奋性突触具有异常的突触小泡聚集和突触后密度伸长、更多的沉默突触和更少的活跃突触,其基础传递增强,释放概率受损。除了这些表型外,我们还观察到突触蛋白磷酸化异常,但神经营养因子信号通路没有差异。与将这些异常磷酸化蛋白与神经精神疾病联系起来的报道一致,突变型 TrkC 敲入小鼠表现出社交反应受损和回避行为增加。因此,通过调节突触蛋白磷酸化,TrkC-PTPσ 复合物对于体内兴奋性突触的成熟而非形成至关重要。