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Activity-Dependent Gene Expression in the Mammalian Olfactory Epithelium

机译:哺乳动物嗅觉上皮中的活性依赖性基因表达

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Activity-dependent processes are important to olfactory sensory neurons (OSNs) in several ways, such as cell survival and the specificity of axonal convergence. The identification of activity-dependent mRNAs has contributed to our understanding of OSN axon convergence, but has revealed surprisingly little about other processes. Published studies of activity-dependent mRNAs in olfactory mucosae overlap poorly, but by combining these agreements with meta-analysis of existing data we identify 443 mRNAs that respond to methods that alter OSN activity. Three hundred and fifty of them are expressed in mature OSNs, consistent with the expectation that activity-dependent responses are cell autonomous and driven by odor stimulation. Many of these mRNAs encode proteins that function at presynaptic terminals or support electrical activity, consistent with hypotheses linking activity dependence to synaptic plasticity and energy conservation. The lack of agreement between studies is due largely to underpowered experiments. In addition, methods used to alter OSN activity are susceptible to indirect or off-target effects. These effects deserve greater attention, not only to rigorously identify OSN mRNAs that respond to altered OSN activity, but also because these effects are of significant interest in their own right. For example, the mRNAs of some sustentacular cell enzymes believed to function in odorant clearance (Cyp2a4 and Cyp2g1) are sensitive to unilateral naris occlusion used to reduce odorant stimulation of the ipsilateral olfactory epithelium. Also problematic are odorant receptor mRNAs, which show little agreement across studies and are susceptible to differences in frequency of expression that masquerade as activity-dependent changes in mRNA abundance.
机译:活性依赖性过程对嗅觉感觉神经元(OSN)以几种方式(例如细胞存活和轴突收敛的特异性)重要。依赖活动的MRNA的识别有助于我们对OSN Axon收敛的理解,但令人惊讶地揭示了其他过程。发表了对嗅觉粘膜活性依赖的MRNA的研究重叠不良,但通过将这些协议与现有数据的荟萃分析相结合,我们识别443 MRNA,响应OSN活动的方法。其中三百五十个以成熟的OSN表示,符合期望,期望活性依赖性反应是细胞的自主,并且由气味刺激驱动。这些MRNA中的许多编码蛋白质在突触前终端或支持电活动中,与假设连接到突触可塑性和节能的假设。研究缺乏协议主要是由于实验提供了很大的影响。此外,用于改变OSN活性的方法易于间接或偏离目标效果。这些效果值得更加关注,不仅要严格地识别响应改变OSN活动的OSN MRNA,还因为这些效应对自己的权利非常感兴趣。例如,在气味清除(CYP2A4和CYP2G1)中致力于在气味清除(CYP2A4和CYP2G1)的一些缓矿细胞酶的MRNA对单侧NARIS闭塞敏感,用于减少同侧嗅觉上皮的气味刺激。还有问题是气味受体MRNA,其跨研究表现出很少的协议,并且易于频率差异的差异,使得经络作为mRNA丰富的活性依赖性变化。

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