Brain Research Centre and Department of Psychiatry, University of British Columbia, Vancouver, BC, Canada V6T 2B5.
Curr Opin Neurobiol. 2011 Feb;21(1):132-43. doi: 10.1016/j.conb.2010.08.016. Epub 2010 Sep 9.
A number of synaptogenic factors induce presynaptic or postsynaptic differentiation when presented to axons or dendrites. Many such factors participate in bidirectional trans-synaptic adhesion complexes. Axonal neurexins interacting in an isoform-specific code with multiple dendritic partners (neuroligins, LRRTMs, or Cbln-GluRδ), and axonal protein tyrosine phosphatase receptors interacting with dendritic NGL-3, nucleate local networks of high-affinity protein-protein interactions leading to aligned presynaptic and postsynaptic differentiation. Additional secreted target-derived factors such as fibroblast growth factors and glial-derived factors such as thrombospondin bind specific axonal or dendritic receptors stimulating signal transduction mechanisms to promote selective aspects of synapse development. Together with classical adhesion molecules and controlled by transcriptional cascades, these synaptogenic adhesion complexes and secreted factors organize the molecular composition and thus functional properties of central synapses.
许多突触形成因子在被递送到轴突或树突时会诱导突触前或突触后分化。许多这样的因子参与双向跨突触黏附复合物。轴突神经连接蛋白以同种型特异性密码与多个树突靶标(神经连接素、LRRTMs 或 Cbln-GluRδ)相互作用,而轴突蛋白酪氨酸磷酸酶受体与树突 NGL-3 相互作用,形成局部高亲和力蛋白-蛋白相互作用网络,导致突触前和突触后分化的对准。其他分泌的靶源性因子,如成纤维细胞生长因子和神经胶质衍生的因子,如血小板反应蛋白,结合特定的轴突或树突受体,刺激信号转导机制,促进突触发育的选择性方面。这些突触形成黏附复合物和分泌因子与经典黏附分子一起,受转录级联调控,组织中枢突触的分子组成,从而调节其功能特性。