首页> 外文期刊>Otology and neurotology: official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology >In vitro growth of human endolymphatic sac cells: a transmission electron microscopic and immunohistochemical study in patients with vestibular schwannoma and Meniere's disease.
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In vitro growth of human endolymphatic sac cells: a transmission electron microscopic and immunohistochemical study in patients with vestibular schwannoma and Meniere's disease.

机译:人内淋巴囊细胞的体外生长:前庭神经鞘瘤和梅尼埃病患者的透射电镜和免疫组织化学研究。

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摘要

HYPOTHESIS: Human endolymphatic sac cells have been notoriously difficult to maintain in culture. It was hypothesized that an in vitro environment intended for growth of keratinocytes would also be suitable for human endolymph sac cells. BACKGROUND: Studies on cell physiology of human endolymphatic sac cells have been hampered by difficulties in maintaining them in culture. METHODS: Human endolymphatic sac cells were taken from 10 patients during translabyrinthine skull base surgery for vestibular schwannoma, one of whom also had Meniere's disease. Cell lines of proliferating epithelial cells were obtained after trypsinization and growth in a 3:1 mixture of Dulbecco's modified Eagle medium and Ham's F12 medium supplemented with 10% fetal calf serum. Fibroblast overgrowth was counteracted by the use of so-called cloning rings. During various stages, cells were investigated with transmission electron microscopy and/or immunohistochemistry. RESULTS: Proliferation took place after 2 to 3 days of primary cell culture. The cells were cytokeratin-positive and pleomorphic, and they had abundant polarized microvillus-like projections, numerous coated cytoplasmic pits and vesicles, and a well-developed rough endoplasmic reticulum. CONCLUSION: Cell lines of proliferating human endolymphatic sac cells can be produced with the technique described here and may be a valid tool in studies of human endolymph sac physiology.
机译:假设:众所周知,人类内淋巴囊细胞很难在培养中维持。假设用于角质形成细胞生长的体外环境也适用于人内淋巴囊细胞。背景:人类内淋巴囊细胞的细胞生理研究由于难以维持其培养而受到阻碍。方法:在经迷路颅底颅底手术的前庭神经鞘瘤患者中,从10例患者中提取了人类淋巴囊细胞,其中一位也患有美尼尔氏病。胰蛋白酶消化并在补充了10%胎牛血清的Dulbecco改良的Eagle培养基和Ham's F12培养基的3:1混合物中进行胰蛋白酶消化和生长后,获得了增殖的上皮细胞系。成纤维细胞的过度生长被所谓的克隆环所抵消。在各个阶段,用透射电子显微镜和/或免疫组织化学研究细胞。结果:原代细胞培养2至3天后发生增殖。这些细胞是细胞角蛋白阳性和多形性的,它们具有丰富的极化的微绒毛状突起,许多包被的细胞质凹坑和囊泡,以及发达的粗面内质网。结论:可使用此处描述的技术生产增殖性人内淋巴囊细胞系,并且可能是研究人内淋巴囊生理学的有效工具。

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