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The superior turbinate as a source of functional human olfactory receptor neurons.

机译:上鼻甲是功能性人类嗅觉受体神经元的来源。

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OBJECTIVES: The function of human olfactory receptor neurons (ORNs) remains incompletely understood, in part because of the difficulty of obtaining viable olfactory tissue for study. During endoscopic sphenoidotomy, a portion of the superior turbinate is often removed to achieve wide and safe access to the sphenoid sinus. The purpose of this study was to determine whether functional olfactory mucosa could be obtained from such superior turbinate tissue. STUDY DESIGN/METHODS: Superior turbinate tissue was resected from 4 patients undergoing transnasal endoscopic approaches to the sphenoid sinus. The gross appearance of the turbinate mucosa was normal at the time of surgery. The specimens were placed directly into cold cell culture media and transferred to the laboratory. A portion of the mucosa was fixed and embedded for histology and immunohistochemistry. The remaining tissue was enzymatically dissociated, and the resulting cell suspension was either prepared for immediate calcium imaging or placed into cell culture. Cultured ORNs underwent calcium imaging after several weeks to assess their ability to respond to odorants. RESULTS: Histologic analysis of superior turbinate tissue revealed the presence of patchy olfactory neuroepithelium staining positive for olfactory marker protein. Acutely dissociated ORNs were capable of generating calcium responses to odorant mixtures. ORNs could be maintained in mixed culture and retained their ability to respond to odorants. CONCLUSIONS: Superior turbinate tissue removed during endoscopic sphenoidotomy can provide a valuable source of human olfactory neuroepithelium for functional or histologic study. Superior turbinate tissue yields stem cells and immature neurons capable of differentiating into ORNs that retain many of their functional characteristics even after growth in culture.
机译:目的:人类嗅觉受体神经元(ORNs)的功能仍未完全了解,部分原因是难以获得可行的嗅觉组织进行研究。在内窥镜下进行蝶窦切开术时,通常会切除一部分上鼻甲,以实现广泛而安全地进入蝶窦。这项研究的目的是确定是否可以从这种上鼻甲组织获得功能性嗅觉粘膜。研究设计/方法:从4例经鼻内窥镜检查蝶窦的患者中切除上鼻甲组织。手术时鼻甲粘膜的总体外观正常。将标本直接放入冷细胞培养基中并转移到实验室。固定一部分粘膜并将其包埋,用于组织学和免疫组织化学。剩余的组织被酶解,然后将所得的细胞悬液制备用于立即钙成像或置于细胞培养物中。培养的ORN在数周后接受了钙成像,以评估其对气味的反应能力。结果:上鼻甲组织的组织学分析表明存在嗅觉标记蛋白阳性的片状嗅觉神经上皮染色。急性离解的ORN能够对加味剂混合物产生钙反应。 ORN可以保持在混合培养中,并保留其对气味的反应能力。结论:内窥镜蝶窦切除术中去除的上鼻甲组织可为功能或组织学研究提供有价值的人嗅觉神经上皮来源。优良的鼻甲组织产生干细胞和不成熟的神经元,它们能够分化为即使在培养物中生长后仍保留许多功能特性的ORN。

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