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Gray, Noah W.

https://orcid.org/0000-0002-4672-7403

Mayo Clinic

Mayo Clinic

Citations 1

A dynamin-3 spliced variant modulates the actin/cortactin-dependent morphogenesis of dendritic spines
Gray, Noah W. , Kruchten, Anne, Chen, Jing , McNiven, Mark A.

Journal of Cell Science | March 2, 2005 | Volume: 118 | Issue: 6 | Pages: 1279-1290

10.1242/jcs.01711 Get It

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.