Boukhtouche Fatiha, Janmaat Sonja, Vodjdani Guilan, Gautheron Vanessa, Mallet Jacques, Dusart Isabelle, Mariani Jean
Université Pierre et Marie Curie-Paris6, Unité Mixte de Recherche 7102-Neurobiologie des Processus Adaptatifs, Centre National de la Recherche Scientifique, UMR 7102-NPA, Paris, F-75005, France.
J Neurosci. 2006 Feb 1;26(5):1531-8. doi: 10.1523/JNEUROSCI.4636-05.2006.
Dendritic differentiation involves both regressive and growth events. The mechanisms controlling the regressive events are poorly understood. This study is aimed at determining the role of the nuclear receptor retinoid-related orphan receptor alpha (RORalpha) in Purkinje cell (PC) dendritic differentiation in organotypic cultures. As observed in vivo, in these cultures, fusiform PCs with embryonic bipolar shape undergo regression before the outgrowth of the ultimate dendritic tree. We show that lentiviral-mediated hRORalpha1 overexpression in fusiform PCs leads to a cell-autonomous accelerated progression of dendritic differentiation. In addition, RORalpha is necessary for the PC regressive events: whereas staggerer RORalpha-deficient PCs remain in the embryonic fusiform stage, replacement of hRORalpha1 restores normal dendritogenesis. These results demonstrate that RORalpha expression in fusiform PCs is crucial for the dendritic regression and progression of the following step of extension of dendritic processes. However, it does not seem to participate to the last stage of dendritic growth. This study identifies RORalpha as a nuclear receptor crucial for the control of dendritic remodeling during development.
树突分化涉及退行性和生长性事件。控制退行性事件的机制目前尚不清楚。本研究旨在确定核受体视黄酸相关孤儿受体α(RORα)在器官型培养物中浦肯野细胞(PC)树突分化中的作用。正如在体内观察到的那样,在这些培养物中,具有胚胎双极形状的梭形PC在最终树突的生长之前会经历退化。我们表明,慢病毒介导的hRORα1在梭形PC中的过表达导致树突分化的细胞自主性加速进展。此外,RORα对于PC的退行性事件是必需的:而 staggerer RORα缺陷型PC停留在胚胎梭形阶段,hRORα1的替代可恢复正常的树突发生。这些结果表明,梭形PC中RORα的表达对于树突的退化以及随后树突延伸步骤的进展至关重要。然而,它似乎并不参与树突生长的最后阶段。本研究确定RORα是在发育过程中控制树突重塑的关键核受体。