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首页> 外文期刊>Molecular and cellular neurosciences >IgSF8: A developmentally and functionally regulated cell adhesion molecule in olfactory sensory neuron axons and synapses
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IgSF8: A developmentally and functionally regulated cell adhesion molecule in olfactory sensory neuron axons and synapses

机译:IgSF8:嗅觉感觉神经元轴突和突触中的发育和功能调节细胞粘附分子。

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摘要

Here, we investigated an Immunoglobulin (Ig) superfamily protein IgSF8 which is abundantly expressed in olfactory sensory neuron (OSN) axons and their developing synapses. We demonstrate that expression of IgSF8 within synaptic neuropil is transitory, limited to the period of glomerular formation. Glomerular expression decreases after synaptic maturation and compartmental glomerular organization is achieved, although expression is maintained at high levels within the olfactory nerve layer (ONL). Immunoprecipitations indicate that IgSF8 interacts with tetraspanin CD9 in the olfactory bulb (OB). CD9 is a component of tetraspanin-enriched microdomains (TEMs), specialized microdomains of the plasma membrane known to regulate cell morphology, motility, invasion, fusion and signaling, in both the nervous and immune systems, as well as in tumors. In vitro, both IgSF8 and CD9 localize to puncta within axons and growth cones of OSNs, consistent with TEM localization. When the olfactory epithelium (OE) was lesioned, forcing OSN regeneration en masse, IgSF8 was once again able to be detected in OSN axon terminals as synapses were reestablished. Finally, we halted synaptic maturation within glomeruli by unilaterally blocking functional activity and found that IgSF8 did not undergo exclusion from this subcellular compartment and instead continued to be detected in adult glomeruli. These data support the hypothesis that IgSF8 facilitates OSN synapse formation.
机译:在这里,我们研究了一种免疫球蛋白(Ig)超家族蛋白IgSF8,该蛋白在嗅觉感觉神经元(OSN)轴突及其发育的突触中大量表达。我们证明突触神经pil中的IgSF8的表达是短暂的,限于肾小球形成的时期。尽管在嗅觉神经层(ONL)中表达保持高水平,但在突触成熟和实现肾小球肾小球组织后,肾小球表达降低。免疫沉淀表明,IgSF8与嗅球(OB)中的四跨膜CD9相互作用。 CD9是富含四跨素的微区(TEM)的组成部分,它是质膜的专门微区,已知在神经和免疫系统以及肿瘤中调节细胞形态,运动性,侵袭,融合和信号传导。在体外,IgSF8和CD9都定位于OSNs的轴突和生长锥内的点状,与TEM定位一致。当嗅觉上皮(OE)受损,迫使OSN再生时,随着突触的重新建立,在OSN轴突末端可以再次检测到IgSF8。最后,我们通过单方面阻断功能活性中止了肾小球内的突触成熟,发现IgSF8并未从该亚细胞区室中排除,而是继续在成年肾小球中被检测到。这些数据支持IgSF8促进OSN突触形成的假说。

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