Gray Noah W, Kruchten Anne E, Chen Jing, McNiven Mark A
Molecular Neuroscience Program and Graduate School, Mayo Clinic, Rochester, MN 55905, USA.
J Cell Sci. 2005 Mar 15;118(Pt 6):1279-90. doi: 10.1242/jcs.01711. Epub 2005 Mar 1.
Immature dendrites extend many actin-rich filopodial structures that can be replaced by synapse-containing dendritic spines as the neuron matures. The large GTPase dynamin-3 (Dyn3) is a component of the postsynapse in hippocampal neurons but its function is undefined. Here, we demonstrate that a specific Dyn3 variant (Dyn3baa) promotes the formation of immature dendritic filopodia in cultured neurons. This effect is dependent upon Dyn3 GTPase activity and a direct interaction with the F-actin-binding protein cortactin. Consistent with these findings, Dyn3baa binds to cortactin with a 200% higher affinity than Dyn3aaa, a near identical isoform that does not induce dendritic filopodia when expressed in cultured neurons. Finally, levels of Dyn3baa-encoding mRNA are tightly regulated during neuronal maturation and are markedly upregulated during synaptogenesis. Together, these findings provide the first evidence that an enhanced interaction between a specific Dyn3 splice variant and cortactin modulate actin-membrane dynamics in developing neurons to regulate the morphogenesis of dendritic spines.
未成熟的树突会延伸出许多富含肌动蛋白的丝状伪足结构,随着神经元成熟,这些结构可被含有突触的树突棘所取代。大型GTP酶动力蛋白3(Dyn3)是海马神经元突触后成分,但其功能尚不清楚。在此,我们证明一种特定的Dyn3变体(Dyn3baa)可促进培养神经元中未成熟树突丝状伪足的形成。这种效应依赖于Dyn3 GTP酶活性以及与F-肌动蛋白结合蛋白皮层肌动蛋白的直接相互作用。与这些发现一致,Dyn3baa与皮层肌动蛋白的结合亲和力比Dyn3aaa高200%,Dyn3aaa是一种几乎相同的异构体,在培养神经元中表达时不会诱导树突丝状伪足形成。最后,编码Dyn3baa的mRNA水平在神经元成熟过程中受到严格调控,在突触形成过程中显著上调。总之,这些发现首次证明特定的Dyn3剪接变体与皮层肌动蛋白之间增强的相互作用可调节发育中神经元的肌动蛋白-膜动力学,从而调控树突棘的形态发生。