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首页> 外文期刊>BMC Oral Health >Evaluation of oral keratinocyte progenitor and T-lymphocite cells response during early healing after augmentation of keratinized gingiva with a 3D collagen matrix - a pilot study
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Evaluation of oral keratinocyte progenitor and T-lymphocite cells response during early healing after augmentation of keratinized gingiva with a 3D collagen matrix - a pilot study

机译:在用3D胶原蛋白基质增强角化牙龈后早期愈合期间评估口腔角质形成细胞祖细胞和T淋巴细胞的反应-一项初步研究

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Background The aim of the present study is to analyze the behavior of selected populations of oral keratinocytes and T-lymphocytes, responsible for re-constructing and maintaining the oral epithelial tissue architecture, following augmentation of the keratinized oral mucosa using a 3D-collagen matrix. Methods Different groups of oral keratinocytes were isolated from biopsies harvested from 3 patients before the surgical procedure, as well as 7 and 14 days after the augmentation procedure. T-lymphocytes were isolated from peripheral blood at same timepoints. Keratinocytes were characterized for stem and differentiation markers, such as p63, cytokeratin 10 and 14, and in vitro parameters, such as cell viability, cell size and colony-forming efficiency. T-lymphocytes were analyzed for viability and the expression of various cluster of differentiation markers. The methods included magnetic separation of cell populations, immunofluorescence, flow cytometry, and histology of oral biopsies. Results Both at 7 and 14 days, the majority of cells that repopulate the matrix were actively proliferating/progenitor oral keratinocytes with the phenotype integrin alfa6beta4?+?CD71+. These cells display in vitro characteristics similar to the progenitor cells analyzed before the matrix placement. T-lymphocytes expressed CD8 and CD69 markers, while CD25 was absent. Conclusion The study shows that two weeks after the collagen membrane placement, the healing process appeared to be histologically complete, with no abnormal immune response induced by the matrix, however, with a higher than usual content of active proliferating cells, the majority of keratinocytes being characterized as transit amplifying cells.
机译:背景技术本研究的目的是分析使用3D胶原蛋白基质增强角化口腔粘膜后,口腔角质形成细胞和T淋巴细胞的选定群体的行为,这些行为负责重建和维持口腔上皮组织结构。方法从3例患者在手术前以及增强手术后第7和14天收集的活检样本中分离出不同种类的口腔角质形成细胞。在相同的时间点从外周血中分离出T淋巴细胞。表征角质形成细胞的干和分化标记,例如p63,细胞角蛋白10和14,以及体外参数,例如细胞生存力,细胞大小和集落形成效率。分析T淋巴细胞的活力和各种分化标记簇的表达。这些方法包括细胞群体的磁分离,免疫荧光,流式细胞术和口腔活检组织学。结果在第7天和第14天,重新填充基质的大多数细胞是具有表型整联蛋白α6β4β+βCD71+的活跃增殖/祖细胞口腔角质形成细胞。这些细胞显示出与基质放置之前分析的祖细胞相似的体外特征。 T淋巴细胞表达CD8和CD69标记,而CD25不存在。结论研究表明,胶原蛋白膜放置后两周,愈合过程在组织学上似乎完成,没有由基质诱导的异常免疫反应,但是,活性增生细胞的含量高于正常水平,大多数角质形成细胞是特征为转运放大细胞。

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