Rattazzi Lorenza, Cariboni Anna, Poojara Ridhika, Shoenfeld Yehuda, D'Acquisto Fulvio
William Harvey Research Institute, Barts and The London School of Medicine and Dentistry Queen Mary University of London, UK.
Department of Pharmacological and Biomolecular Sciences, University of Milan Milan, Italy ; Department of Cell Biology, Institute of Ophthalmology, University College London London, UK.
Front Neurosci. 2015 Sep 9;9:318. doi: 10.3389/fnins.2015.00318. eCollection 2015.
Immune deficiencies are often associated with a number of physical manifestations including loss of sense of smell and an increased level of anxiety. We have previously shown that T and B cell-deficient recombinase activating gene (RAG-1)(-∕-) knockout mice have an increased level of anxiety-like behavior and altered gene expression involved in olfaction. In this study, we expanded these findings by testing the structure and functional development of the olfactory system in RAG-1 (-∕-) mice. Our results show that these mice have a reduced engagement in different types of odors and this phenotype is associated with disorganized architecture of glomerular tissue and atrophy of the main olfactory epithelium. Most intriguingly this defect manifests specifically in adult age and is not due to impairment in the patterning of the olfactory neuron staining at the embryo stage. Together these findings provide a formerly unreported biological evidence for an altered function of the olfactory system in RAG-1 (-∕-) mice.
免疫缺陷通常与多种身体表现有关,包括嗅觉丧失和焦虑水平升高。我们之前已经表明,T细胞和B细胞缺陷的重组激活基因(RAG-1)(-/-)敲除小鼠的焦虑样行为水平增加,并且参与嗅觉的基因表达发生改变。在本研究中,我们通过测试RAG-1(-/-)小鼠嗅觉系统的结构和功能发育来扩展这些发现。我们的结果表明,这些小鼠对不同类型气味的反应减少,并且这种表型与肾小球组织结构紊乱和主要嗅觉上皮萎缩有关。最有趣的是,这种缺陷在成年期特异性表现,并非由于胚胎期嗅觉神经元染色模式受损所致。这些发现共同为RAG-1(-/-)小鼠嗅觉系统功能改变提供了以前未报道的生物学证据。