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Exfoliated Human Olfactory Neuroepithelium: A Source of Neural Progenitor Cells

机译:灭绝的人嗅神经脑膜炎:神经祖细胞的源

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Abstract Neural progenitor cells (NPC) contained in the human adult olfactory neuroepithelium (ONE) possess an undifferentiated state, the capability of self-renewal, the ability to generate neural and glial cells as well as being kept as neurospheres in cell culture conditions. Recently, NPC have been isolated from human or animal models using high-risk surgical methods. Therefore, it was necessary to improve methodologies to obtain and maintain human NPC as well as to achieve better knowledge of brain disorders. In this study, we propose the establishment and characterization of NPC cultures derived from the human olfactory neuroepithelium, using non-invasive procedures. Twenty-two healthy individuals (29.7?±?4.5 years of age) were subjected to nasal exfoliation. Cells were recovered and kept as neurospheres under serum-free conditions. The neural progenitor origin of these neurospheres was determined by immunocytochemistry and qPCR. Their ability for self-renewal and multipotency was analyzed by clonogenic and differentiation assays, respectively. In the cultures, the ONE cells preserved the phenotype of the neurospheres. The expression levels of Nestin, Musashi, Sox2, and βIII-tubulin demonstrated the neural origin of the neurospheres; 48% of the cells separated could generate neurospheres, determining that they retained their self-renewal capacity. Neurospheres were differentiated in the absence of growth factors (EGF and FGF), and their multipotency ability was maintained as well. We were also able to isolate and grow human neural progenitor cells (neurospheres) through nasal exfoliates (non-invasive method) of the ONE from healthy adults, which is an extremely important contribution for the study of brain disorders and for the development of new therapies.
机译:摘要人成人嗅觉神经早期(一)中含有的神经祖细胞(NPC)具有未分化的状态,自我更新的能力,产生神经和胶质细胞的能力,以及作为细胞培养条件的神经球体。最近,NPC使用高风险手术方法从人或动物模型中分离出来。因此,有必要改进方法,以获得和维持人NPC,并达到更好地了解脑疾病。在这项研究中,我们提出了使用非侵入性程序的衍生自人嗅觉神经早期的NPC培养物的建立和表征。二十二个健康个体(29.7?±4.5岁)患有鼻腔去角质。回收细胞并保持在无血清条件下的神经球。通过免疫细胞化学和QPCR测定这些神经球的神经祖的起源。它们分别通过克隆语和分化测定分析了自我更新和多因素的能力。在培养物中,一种细胞保留了神经球的表型。 Nestin,Musashi,Sox2和βIII-小管蛋白的表达水平证明了神经球的神经来源; 48%分离的细胞可以产生神经球,确定它们保留了它们的自我更新能力。在没有生长因子(EGF和FGF)的情况下,神经球分化,并且它们也保持了它们的多能力。我们还能够通过来自健康成人的鼻去角质(非侵入性方法)孤立和生长人类神经祖细胞(神经球),这对于脑疾病和新疗法的发展是一种极为重要的贡献。

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