Failed Cytokinesis of Neural Progenitors in Citron Kinase-Deficient Rats Leads to Multiciliated Neurons

被引:19
作者
Anastas, Sara B. [1 ]
Mueller, Dorit [1 ]
Semple-Rowland, Susan L. [1 ]
Breunig, Joshua J. [2 ]
Sarkisian, Matthew R. [1 ]
机构
[1] Univ Florida, Dept Neurosci, McKnight Brain Inst, Gainesville, FL 32610 USA
[2] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06510 USA
关键词
cortical malformation; forebrain development; pericentrin; primary cilia; neuronal differentiation; PROTEIN-COUPLED-RECEPTORS; BARDET-BIEDL-SYNDROME; PRIMARY CILIA; FLATHEAD MUTANT; BRAIN; DISEASE; ABNORMALITIES; NEUROGENESIS; LOCALIZATION; APOPTOSIS;
D O I
10.1093/cercor/bhq099
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Most, if not all, cortical neurons possess a single primary cilium; however, little is known about the mechanisms that control neuronal ciliogenesis. The Citron kinase-deficient (Citron-K-fh/fh) rat, a model in which failed cytokinesis during development produces cortical neurons containing multiple cellular organelles, provides a unique system in which to examine the relationship between centriole inheritance and neuronal ciliogenesis. In this study, we analyzed the cerebral cortex of these animals using immunohistochemistry, serial confocal, and electron microscopy to determine if the multinucleated neurons present in the cortex of these animals also possess multiple centrioles and cilia. We found that neurons containing multiple nuclei possessed multiple centrioles and cilia whose lengths varied across cortical regions. Despite the presence of multiple cilia, we found that perinatal expression of adenylyl cyclase III, a cilia-specific marker, and somatostatin receptor 3, a receptor enriched in cilia, were preserved in developing Citron-K-fh/fh brain. Together, these results show that multinucleated neurons arising from defective cytokinesis can extend multiple cilia.
引用
收藏
页码:338 / 344
页数:7
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