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Influence of olfactory bulb on dendritic knob density of rat olfactory receptor neurons in vitro.嗅球对体外培养的大鼠嗅觉受体神经元树突棘密度的影响。
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Olfactory ensheathing cells abutting the embryonic olfactory bulb express Frzb, whose deletion disrupts olfactory axon targeting.嗅鞘细胞贴附在胚胎嗅球上表达 Frzb,其缺失会破坏嗅神经轴突的靶向性。
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Global expression profiling of globose basal cells and neurogenic progression within the olfactory epithelium.嗅上皮内球形基底细胞的全局表达谱和神经发生进展。
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Coculture of the vomeronasal organ and olfactory bulb of the fetal rat.
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Mitral cell differentiation and synaptogenesis of rat presumptive olfactory bulb in organ culture.大鼠嗅球原基在器官培养中的二尖瓣细胞分化与突触形成
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Molecular cloning and sequencing of a cDNA for olfactory marker protein.嗅觉标记蛋白cDNA的分子克隆与测序
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Electron-microscopic demonstration of olfactory-marker protein with protein G-gold in freeze-substituted, Lowicryl K11M-embedded rat olfactory-receptor cells.在经冷冻置换、用Lowicryl K11M包埋的大鼠嗅觉受体细胞中,用蛋白G-金对嗅觉标记蛋白进行电子显微镜显示。
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嗅球增加嗅觉受体细胞中的标记蛋白。

Olfactory bulb increases marker protein in olfactory receptor cells.

作者信息

Chuah M I, Farbman A I

出版信息

J Neurosci. 1983 Nov;3(11):2197-205. doi: 10.1523/JNEUROSCI.03-11-02197.1983.

DOI:10.1523/JNEUROSCI.03-11-02197.1983
PMID:6355401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6564630/
Abstract

Olfactory mucosa was excised from the heads of embryonic day 15 (E15) rat fetuses, prior to the appearance of olfactory marker protein (OMP), and cultured with or without the presumptive olfactory bulb. Specific immunohistochemical staining for the OMP was detected in both groups of explants 6 days after explantation. At no time do the supporting cells and basal cells show positive OMP staining. Results of radioimmunoassay on the two groups of cultures showed that about twice as much OMP was present in organ cultures grown with presumptive olfactory bulb. Estimates of the area of olfactory mucosa in the explants revealed no significant differences between those cultured with or without the bulb. Cell counts revealed that the increased amount of OMP in explants with the bulb was due to a higher number of OMP-positive receptor neurons. Explants of olfactory mucosa cultured with other tissues (cerebrum, cerebellum, cervical spinal cord, and heart) contained approximately the same amount of OMP as explants of mucosa alone; i.e., these other tissues did not enhance OMP levels. Similarly, there was no enhancement of OMP level when the olfactory mucosa was separated from the bulb by a Millipore filter of 0.45 micron pore size. Thus the results of the study indicate that the presumptive olfactory bulb specifically increases OMP level by a mechanism that requires direct contact between the receptor cells and bulb.

摘要

在嗅标记蛋白(OMP)出现之前,从胚胎第15天(E15)大鼠胎儿的头部切除嗅黏膜,并在有或没有假定嗅球的情况下进行培养。移植6天后,在两组外植体中均检测到OMP的特异性免疫组织化学染色。支持细胞和基底细胞在任何时候都未显示OMP染色阳性。两组培养物的放射免疫分析结果表明,在有假定嗅球生长的器官培养物中,OMP的含量约为前者的两倍。对外植体中嗅黏膜面积的估计显示,有或没有嗅球培养的外植体之间没有显著差异。细胞计数显示,有嗅球的外植体中OMP含量增加是由于OMP阳性受体神经元数量增加。与其他组织(大脑、小脑、颈脊髓和心脏)一起培养的嗅黏膜外植体中OMP的含量与单独的黏膜外植体大致相同;即,这些其他组织并未提高OMP水平。同样,当用孔径为0.45微米的微孔滤膜将嗅黏膜与嗅球分离时,OMP水平也没有提高。因此,该研究结果表明,假定的嗅球通过一种需要受体细胞与嗅球直接接触的机制特异性地提高OMP水平。