Department of Basic Biomedical Science, College of Medicine, Florida Atlantic University, Boca Raton, FL 33431, USA.
Exp Neurol. 2013 Mar;241:125-37. doi: 10.1016/j.expneurol.2012.12.010. Epub 2012 Dec 21.
The olfactory system continuously incorporates new neurons into functional circuits throughout life. Axons from olfactory sensory neurons (OSNs) in the nasal cavity synapse on mitral, tufted and periglomerular (PG) cells in the main olfactory bulb, and low levels of turnover within the OSN population results in ingrowth of new axons under normal physiological conditions. Subpopulations of bulb interneurons are continually eliminated by apoptosis, and are replaced by new neurons derived from progenitors in the adult forebrain subventricular zone. Integration of new neurons, including PG cells that are contacted by sensory axons, leads to ongoing reorganization of adult olfactory bulb circuits. The mechanisms regulating this adaptive structural plasticity are not all known, but the process is reminiscent of early nervous system development. Neurotrophic factors have well-established roles in controlling neuronal survival and connectivity during development, leading to speculation that trophic interactions between OSNs and their target bulb neurons may mediate some of these same processes in adults. A number of different trophic factors and their cognate receptors are expressed in the adult olfactory pathway. Neurotrophin-3 (NT3) is among these, as reflected by beta-galactosidase expression in transgenic reporter mice expressing lacZ under the NT3 promoter. Using a combination of approaches, including immunocytochemistry, real-time PCR of laser-captured RNA, and adenovirus-mediated gene transfer of NT3 fusion peptides in vivo, we demonstrate that OSNs express and anterogradely transport NT3 to the olfactory bulb. We additionally observe that in mice treated with adenovirus encoding NT3 tagged with hemagglutinin (HA), a subset of bulb neurons expressing the TrkC neurotrophin receptor are immunoreactive for HA, suggesting their acquisition of the fusion peptide from infected sensory neurons. Our results therefore provide evidence that OSNs may serve as an afferent source of trophic signals for the adult mouse olfactory bulb.
嗅觉系统在整个生命过程中不断将新神经元纳入功能性回路。鼻腔中的嗅觉感觉神经元(OSN)的轴突与嗅球中的主嗅球中的僧帽细胞、丛状细胞和旁嗅小球(PG)细胞形成突触,而 OSN 群体中的低水平更替导致在正常生理条件下新轴突的向内生长。嗅球中间神经元的亚群不断通过细胞凋亡被消除,并被来自成年前脑侧脑室下区祖细胞的新神经元所取代。新神经元的整合,包括与感觉轴突接触的 PG 细胞,导致成年嗅球回路的持续重组。调节这种适应性结构可塑性的机制并非全部已知,但该过程让人联想到早期神经系统发育。神经营养因子在控制发育过程中的神经元存活和连接方面具有明确的作用,这导致人们推测 OSN 与其靶标嗅球神经元之间的营养相互作用可能介导成年个体中的一些相同过程。许多不同的神经营养因子及其同源受体在成年嗅觉通路中表达。神经营养因子-3(NT3)就是其中之一,这反映在表达 lacZ 的转基因报告小鼠中,其 NT3 启动子下的β-半乳糖苷酶表达。我们使用多种方法,包括免疫细胞化学、激光捕获 RNA 的实时 PCR 和体内 NT3 融合肽的腺病毒介导基因转移,证明 OSN 表达并顺行转运 NT3 到嗅球。我们还观察到,在接受编码 NT3 标记有血凝素(HA)的腺病毒处理的小鼠中,表达 TrkC 神经营养因子受体的嗅球神经元亚群对 HA 呈免疫反应性,表明它们从感染的感觉神经元获得融合肽。因此,我们的结果提供了证据表明 OSN 可能作为成年小鼠嗅球的传入营养信号源。