Richard Marion, Sacquet Joëlle, Jourdan François, Pellier-Monnin Véronique
Laboratoire Neurosciences Sensorielles, Comportement, Cognition, CNRS-UMR 5020, Université de Lyon, Lyon 1, F-69366, France.
Brain Res. 2009 Feb 3;1252:52-65. doi: 10.1016/j.brainres.2008.11.049. Epub 2008 Nov 27.
The myelin-associated inhibitory proteins (Nogo-A, MAG and OMgp) that prevent axon regeneration in adult CNS, mediate their effects via a receptor referred as NgR1. Beside their inhibitory role in the adult CNS, Nogo-A and NgR1 might also be functionally involved in the developing nervous system. At the present time, no detailed study is available regarding either the onset of NgR1 expression during development or its spatio-temporal pattern of expression relative to the presence of Nogo-A. Two homologs of NgR1, NgR2 and NgR3, have been recently identified, but their function in the nervous system is still unknown in adult as well as during development. We have examined the spatio-temporal expression pattern of both NgR1, NgR2 and NgR3 mRNAs and corresponding proteins in the developing rat olfactory system using in situ hybridization and immunohistochemistry. From E15-E16 onwards, NgR1 mRNA was expressed by differentiating neurons in both the olfactory epithelium and the olfactory bulb. At all developmental stages, including adult animals, NgR1 protein was preferentially targeted to olfactory axons emerging from the olfactory epithelium. Using double-immunostainings in the postnatal olfactory mucosa, we confirm the neuronal localization of NgR1 and its preferential distribution along the olfactory axons. The NgR2 and NgR3 transcripts and their proteins display similar expression profiles in the olfactory system. Together, our data suggest that, in non-pathological conditions, NgR1 and its homologs may play a role in axon outgrowth in the rat olfactory system and may be relevant for the confinement of neural projections within the developing olfactory bulb.
髓鞘相关抑制蛋白(Nogo-A、MAG和OMgp)可阻止成体中枢神经系统中的轴突再生,它们通过一种名为NgR1的受体发挥作用。除了在成体中枢神经系统中的抑制作用外,Nogo-A和NgR1在发育中的神经系统中可能也具有功能作用。目前,关于发育过程中NgR1表达的起始时间或其相对于Nogo-A存在的时空表达模式,尚无详细研究。最近已鉴定出NgR1的两个同源物NgR2和NgR3,但它们在成体以及发育过程中的神经系统功能仍不清楚。我们使用原位杂交和免疫组织化学方法,研究了发育中的大鼠嗅觉系统中NgR1、NgR2和NgR3 mRNA及相应蛋白的时空表达模式。从胚胎第15-16天起,嗅觉上皮和嗅球中正在分化的神经元表达NgR1 mRNA。在包括成年动物在内的所有发育阶段,NgR1蛋白优先定位于从嗅觉上皮发出的嗅觉轴突。通过对出生后嗅觉黏膜进行双重免疫染色,我们证实了NgR1的神经元定位及其沿嗅觉轴突的优先分布。NgR2和NgR3转录本及其蛋白在嗅觉系统中显示出相似的表达谱。总之,我们的数据表明,在非病理条件下,NgR1及其同源物可能在大鼠嗅觉系统的轴突生长中发挥作用,并且可能与发育中的嗅球内神经投射的限制有关。