Department of Neuroscience and Jefferson Synaptic Biology Center, The Vickie and Jack Farber Institute, Jefferson Hospital for Neuroscience, Thomas Jefferson University, Suite 461, 900 Walnut Street, Philadelphia, PA 19107, USA.
Department of Neuroscience and Jefferson Synaptic Biology Center, The Vickie and Jack Farber Institute, Jefferson Hospital for Neuroscience, Thomas Jefferson University, Suite 461, 900 Walnut Street, Philadelphia, PA 19107, USA; Department of Neurobiology and Behavior, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi City, Gunma 371-8511, Japan.
Neuron. 2018 May 16;98(4):767-782.e8. doi: 10.1016/j.neuron.2018.04.011. Epub 2018 May 3.
Dendritic filopodia select synaptic partner axons by interviewing the cell surface of potential targets, but how filopodia decipher the complex pattern of adhesive and repulsive molecular cues to find appropriate contacts is unknown. Here, we demonstrate in cortical neurons that a single cue is sufficient for dendritic filopodia to reject or select specific axonal contacts for elaboration as synaptic sites. Super-resolution and live-cell imaging reveals that EphB2 is located in the tips of filopodia and at nascent synaptic sites. Surprisingly, a genetically encoded indicator of EphB kinase activity, unbiased classification, and a photoactivatable EphB2 reveal that simple differences in the kinetics of EphB kinase signaling at the tips of filopodia mediate the choice between retraction and synaptogenesis. This may enable individual filopodia to choose targets based on differences in the activation rate of a single tyrosine kinase, greatly simplifying the process of partner selection and suggesting a general principle.
树突状丝状伪足通过“面试”潜在目标细胞表面来选择突触伙伴轴突,但丝状伪足如何解读复杂的黏附和排斥分子线索模式以找到合适的接触点尚不清楚。本文中,我们在皮质神经元中证明,单个线索足以使树突状丝状伪足排斥或选择特定的轴突接触点来进行精细加工作为突触部位。超分辨率和活细胞成像显示 EphB2 位于丝状伪足的尖端和新形成的突触部位。令人惊讶的是,EphB 激酶活性的遗传编码指示剂、无偏分类和光活化 EphB2 揭示了丝状伪足尖端 EphB 激酶信号转导的动力学的简单差异介导了回缩和突触发生之间的选择。这可能使单个丝状伪足能够基于单个酪氨酸激酶的激活率的差异来选择靶标,极大地简化了伙伴选择过程,并提出了一个普遍原则。