Interdisciplinary Graduate Program in Brain Science, Department of Cell and Developmental Biology, Dental Research Institute, Seoul National University, Seoul 110-740, Republic of Korea.
J Neurosci. 2010 Jun 16;30(24):8138-50. doi: 10.1523/JNEUROSCI.0256-10.2010.
The bone morphogenetic protein (BMP) ligand Glass bottom boat (Gbb) acts as a retrograde growth signal at the Drosophila neuromuscular junction (NMJ). Endocytic regulation of presynaptic BMP receptors has been proposed to attenuate retrograde BMP signaling. However, it remains unknown whether the Gbb signal is also regulated by postsynaptic mechanisms. Here, we provide evidence that Drosophila Cdc42-interacting protein 4 (dCIP4) functions postsynaptically to inhibit synaptic growth. dCIP4 is localized postsynaptically at NMJs. dcip4 mutations lead to synaptic overgrowth and increased presynaptic phosphorylated mothers against decapentaplegic (Mad) levels, and these defects are rescued by muscle-specific expression of dCIP4. Biochemical and genetic analyses demonstrate that dCIP4 acts downstream of Cdc42 to activate the postsynaptic Wsp-Arp2/3 pathway. We also show that BMP signaling is necessary for synaptic overgrowth in larvae lacking postsynaptic dcip4 or wsp. Finally, dCIP4 and Wsp inhibit Gbb secretion. Thus, we propose that dCIP4 restrains synaptic growth by inhibiting postsynaptic Gbb secretion through the Wsp-Arp2/3 pathway.
骨形态发生蛋白(BMP)配体 Glass bottom boat(Gbb)在果蝇神经肌肉接点(NMJ)作为逆行生长信号发挥作用。已经提出了内吞调节突触前 BMP 受体以减弱逆行 BMP 信号的假说。然而,Gbb 信号是否也受到突触后机制的调节仍然未知。在这里,我们提供证据表明果蝇 Cdc42 相互作用蛋白 4(dCIP4)在突触后发挥作用以抑制突触生长。dCIP4 在 NMJs 中定位于突触后。dcip4 突变导致突触过度生长和增加的突触前磷酸化母亲对抗 decapentaplegic(Mad)水平,并且这些缺陷可以通过肌肉特异性表达 dCIP4 得到挽救。生化和遗传分析表明,dCIP4 作为 Cdc42 的下游分子激活突触后 Wsp-Arp2/3 途径。我们还表明,在缺乏突触后 dcip4 或 wsp 的幼虫中,BMP 信号对于突触过度生长是必需的。最后,dCIP4 和 Wsp 抑制 Gbb 的分泌。因此,我们提出 dCIP4 通过 Wsp-Arp2/3 途径抑制突触后 Gbb 的分泌来限制突触生长。