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首页> 外文期刊>Journal of Oral and Maxillofacial Pathology >Characterization of oral fibroblasts: An in vitro model for oral fibrosis
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Characterization of oral fibroblasts: An in vitro model for oral fibrosis

机译:口腔成纤维细胞的表征:口腔纤维化的体外模型

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Background: Oral submucous fibrosis (OSMF) is a chronic debilitating condition of the oral mucosa that has been classified as a potentially malignant disorder with a malignant transformation rate of 2%–8%. Several in vitro and in vivo experiments have been performed to formulate a treatment modality for OSMF, yet no ideal in vitro primary oral fibroblast model has been developed. Aim: To establish an in vitro primary oral fibroblast model. Setting and Design: In vitro laboratory setting. Materials and Methodology: Primary cell culture protocol was performed after obtaining normal oral tissue. Karyotyping was performed to rule out chromosomal abnormalities. Immunofluorescence staining was carried with a panel of fibroblast-specific markers (vimentin, phalloidin, transforming growth factor-β receptor 1 [TGFβR1] and s100a4) and Masson trichrome staining (MTS) to demonstrate the presence of extracellular matrix (ECM) qualitatively. Results: A monolayer of oral fibroblasts was observed on the 9supth/sup-day postseeding. No chromosomal abnormality was observed in the patient samples. Positive staining was observed with vimentin, phalloidin, TGFβR1 and s100a4, thereby confirming the cell type. MTS revealed fibroblasts with spindle morphology and scanty ECM. Conclusion: The present study lays down a protocol to design and characterize primary buccal fibroblast cell culture model that would aid researchers in performing in vitro preliminary experiments in areas concerning fibrosis.
机译:背景:口腔粘膜下纤维化(OSMF)是口腔粘膜的一种慢性衰弱性疾病,已被分类为潜在的恶性疾病,其恶性转化率为2%–8%。已经进行了若干体外和体内实验以制定OSMF的治疗方式,但尚未开发出理想的体外初级口腔成纤维细胞模型。目的:建立体外原发性口腔成纤维细胞模型。设置和设计:体外实验室设置。材料和方法:获得正常口腔组织后进行原代细胞培养方案。进行核型分析以排除染色体异常。用一组成纤维细胞特异性标志物(波形蛋白,鬼笔环肽,转化生长因子-β受体1 [TGFβR1]和s100a4)和Masson三色染色(MTS)进行免疫荧光染色,以定性证明细胞外基质(ECM)的存在。结果:接种后第9天观察到单层口腔成纤维细胞。在患者样品中未观察到染色体异常。用波形蛋白,鬼笔环肽,TGFβR1和s100a4观察到阳性染色,从而确认了细胞类型。 MTS显示成纤维细胞具有纺锤体形态和很少的ECM。结论:本研究提出了设计和表征原发性颊成纤维细胞培养模型的协议,该协议将有助于研究人员在涉及纤维化的领域进行体外初步实验。

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