Biederer Thomas
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, USA.
Sci STKE. 2005 Mar 8;2005(274):pe9. doi: 10.1126/stke.2742005pe9.
The signals mediating synaptic differentiation are critical for our understanding of synapse formation and nervous system development. Recent progress highlights the roles of membrane-bound and soluble signaling pathways in this process. The postsynaptic adhesion molecules neuroligin-1, neuroligin-2, and SynCAM1 provide target-derived signals leading to the assembly of presynaptic terminals. In the reverse direction, neuroligins also relay signals into postsynaptic sites through interactions with their presynaptic partners, the beta-neurexins. This adhesion-based system helps to determine the neurotransmitter specificity of postsynaptic specializations. In addition, soluble molecules are released from target neurons and initiate presynaptic differentiation, as demonstrated for the fibroblast growth factor FGF-22. This Perspective summarizes new insights into early synaptic differentiation signals and discusses underlying principles.
介导突触分化的信号对于我们理解突触形成和神经系统发育至关重要。最近的进展突出了膜结合和可溶性信号通路在这一过程中的作用。突触后粘附分子神经连接蛋白-1、神经连接蛋白-2和突触细胞粘附分子1提供源自靶标的信号,导致突触前终末的组装。在相反方向上,神经连接蛋白也通过与其突触前伴侣β-神经突触素相互作用将信号传递到突触后位点。这种基于粘附的系统有助于确定突触后特化的神经递质特异性。此外,可溶性分子从靶神经元释放并启动突触前分化,成纤维细胞生长因子FGF-22的情况就是如此。本综述总结了对早期突触分化信号的新见解,并讨论了潜在原理。