A novel role for CAMKIIβ in the regulation of cortical neuron migration: implications for neurodevelopmental disorders. Issue 11 (November 2018)

• Record Type: Journal Article
• Authors: Nicole, Olivier; Bell, Donald; Leste-Lasserre, Thierry; Doat, Hélène; Guillemot, François; Pacary, Emilie
• Is Part Of: Molecular psychiatry. Volume 23:Issue 11(2018)
• Page Start: 2209
• Page End: 2226
• Publication Date: 2018-11
• Subjects: Mental illness -- Periodicals; Molecular biology -- Periodicals; Neurosciences -- Periodicals; Maladies mentales -- Périodiques; Biologie moléculaire -- Périodiques; Neurosciences -- Périodiques; Psychiatry; Mental illness; Molecular biology; Neurosciences; Moleculaire biologie; Psychiatrie; Psychische stoornissen; Mental Disorders -- Periodicals; Molecular Biology -- Periodicals; Neurosciences -- Periodicals; Electronic journals; Periodicals; 616.89
• DOI: 10.1038/s41380-018-0046-0
• Languages: English
• ISSNs: 1359-4184

Abstract

Abstract Perturbation ofCaMKIIβ expression has been associated with multiple neuropsychiatric diseases, highlightingCaMKIIβ as a gene of interest. Yet, in contrast to CaMKIIα, the specific functions of CaMKIIβ in the brain remain poorly explored. Here, we reveal a novel function for this CaMKII isoform in vivo during neuronal development. By using in utero electroporation, we show that CaMKIIβ is an important regulator of radial migration of projection neurons during cerebral cortex development. Knockdown ofCaMKIIβ causes accelerated migration of nascent pyramidal neurons, whereas overexpression of CaMKIIβ inhibits migration, demonstrating that precise regulation of CaMKIIβ expression is required for correct neuronal migration. More precisely, CaMKIIβ controls the multipolar–bipolar transition in the intermediate zone and locomotion in the cortical plate through its actin-binding and -bundling activities. In addition, our data indicate that a fine-tuned balance between CaMKIIβ and cofilin activities is necessary to ensure proper migration of cortical neurons. Thus, our findings define a novel isoform-specific function for CaMKIIβ, demonstrating that CaMKIIβ has a major biological function in the developing brain.