First Author | Winkler SC | Year | 2020 |
Journal | Mol Neurobiol | Volume | 57 |
Issue | 12 | Pages | 5150-5166 |
PubMed ID | 32860158 | Mgi Jnum | J:336786 |
Mgi Id | MGI:6757594 | Doi | 10.1007/s12035-020-02038-6 |
Citation | Winkler SC, et al. (2020) PKCgamma-Mediated Phosphorylation of CRMP2 Regulates Dendritic Outgrowth in Cerebellar Purkinje Cells. Mol Neurobiol 57(12):5150-5166 |
abstractText | The signalling protein PKCgamma is a major regulator of Purkinje cell development and synaptic function. We have shown previously that increased PKCgamma activity impairs dendritic development of cerebellar Purkinje cells. Mutations in the protein kinase Cgamma gene (PRKCG) cause spinocerebellar ataxia type 14 (SCA14). In a transgenic mouse model of SCA14 expressing the human S361G mutation, Purkinje cell dendritic development is impaired in cerebellar slice cultures similar to pharmacological activation of PKC. The mechanisms of PKCgamma-driven inhibition of dendritic growth are still unclear. Using immunoprecipitation-coupled mass spectrometry analysis, we have identified collapsin response mediator protein 2 (CRMP2) as a protein interacting with constitutive active PKCgamma(S361G) and confirmed the interaction with the Duolink proximity ligation assay. We show that in cerebellar slice cultures from PKCgamma(S361G)-mice, phosphorylation of CRMP2 at the known PKC target site Thr555 is increased in Purkinje cells confirming phosphorylation of CRMP2 by PKCgamma. miRNA-mediated CRMP2 knockdown decreased Purkinje cell dendritic outgrowth in dissociated cerebellar cultures as did the transfection of CRMP2 mutants with a modified Thr555 site. In contrast, dendritic development was normal after wild-type CRMP2 overexpression. In a novel knock-in mouse expressing only the phospho-defective T555A-mutant CRMP2, Purkinje cell dendritic development was reduced in dissociated cultures. This reduction could be rescued by transfecting wild-type CRMP2 but only partially by the phospho-mimetic T555D-mutant. Our findings establish CRMP2 as an important target of PKCgamma phosphorylation in Purkinje cells mediating its control of dendritic development. Dynamic regulation of CRMP2 phosphorylation via PKCgamma is required for its correct function. |