RESUMEN
Subsequently to the publication of the above article, the authors have realized that the secondlisted author, The Mon La, had not been properly credited as one of the cowriters of the paper. Therefore, the Authors' Contributions of the Declarations section of the article should have read as follows: Authors' contributions HY, KTa and TML designed the research and wrote the paper. HY, TA, YM, EO and TT performed mutant protein construction, protein purification and actin bundling experiments. TA and YM performed electron microscopy. EO, TML, KS and KF performed immunofluorescent microscopy, cell migration assay and analyzed data. FYW and KTo identified phosphorylation sites by MALDIMS. All authors read and approved the final manuscript. The authors apologize to the readership of the Journal for the misinformation in this regard, and for any inconvenience caused. [the original article was published in International Journal of Oncology 54: 550558, 2019; DOI: 10.3892/ijo.2018.4663].
RESUMEN
Dynamin copolymerizes with cortactin to form a ringlike complex that bundles and stabilizes actin filaments. Actin bundle formation is crucial for generation of filopodia and lamellipodia, which guide migration, invasion, and metastasis of cancer cells. However, it is unknown how the dynamincortactin complex regulates actin bundle formation. The present study investigated phosphorylation of cortactin by cyclindependent kinase 5 (CDK5) and its effect on actin bundle formation by the dynamincortactin complex. CDK5 directly phosphorylated cortactin at T145/T219 in vitro. Phosphomimetic mutants in which one or both of these threonine residues was substituted by aspartate were used. The three phosphomimetic mutants (T145D, T219D and T145DT219D) had a decreased affinity for Factin. Furthermore, electron microscopy demonstrated that these phosphomimetic mutants could not form a ringlike complex with dynamin 1. Consistently, the dynamin 1phosphomimetic cortactin complexes exhibited decreased actinbundling activity. Expression of the phosphomimetic mutants resulted in not only aberrant lamellipodia and short filopodia but also cell migration in NG10815 gliomaderived cells. These results indicate that phosphorylation of cortactin by CDK5 regulates formation of lamellipodia and filopodia by modulating dynamin 1/cortactindependent actin bundling. Taken together, these findings suggest that CDK5 is a potential molecular target for anticancer therapy.