Abstract

To investigate the effect of Malassez epithelial surplus in inflammatory periodontal tissues on the number and differentiation ability of periodontal stem cells. 30 patients with periodontitis admitted to the hospital from November 2014 to April 2017 were selected as the observation group. A total of 30 healthy oral examination patients were selected as control group. Periodontal tissue in the 2 groups were taken and the periodontal ligament cells, the complete inflammatory periodontal ligament stem cells by using the low density screening, purification, and periodontal tissue were obtained by using differential digestion method of Malassez epithelial remaining, were observed under inverted microscope in the periodontal tissue Malassez epithelial residual form, will be in the periodontal tissue Malassez epithelial surplus together with inflammatory periodontal ligament stem cells, RT-PCR technique has been applied to the determination of ALP and Runx-2 mRNA expression level to observe the differentiation ability. Flow cytometry showed that the cell markers CD29 and CD90 in the cultured periodontal stem cells were positive (88.9% and 99.7%, respectively). A hematopoietic stem cell marker CD45 was negative (0.3%). The inverted microscope results showed that the residual epithelial cells of Malassez, isolated and cultured, had a large nuclear to cytoplasmic ratio, and the different cells were arranged relatively closely, with the overall cell structure of paving stone. The expression levels of ALP and runx-2 mRNA in the observation group were higher than those in the control group (P<0.05). Malassez epithelial surplus in inflammatory periodontal tissues can promote the proliferation of periodontal stem cells and improve the ability of osteogenic differentiation.

Highlights

  • 参考文献 [1] Andreas N, Carl-Peter C, Michael R, et al The Comprehensive AOCMF Classification System: Condylar Process Fractures-Level 3 Tutorial [J]

  • 30 patients with periodontitis admitted to the hospital from November 2014

  • to April 2017 were selected as the observation group

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Summary

Introduction

参考文献 [1] Andreas N, Carl-Peter C, Michael R, et al The Comprehensive AOCMF Classification System: Condylar Process Fractures-Level 3 Tutorial [J]. 织并获得牙周膜细胞,利用低密度法完成炎症牙周膜干细胞的筛选、纯化,利用差速消化法获得牙周组织中Malassez 上皮剩余,倒置显微镜下观察牙周组织中Malassez上皮剩余形态,将牙周组织中Malassez上皮剩余与炎症牙周膜干细 胞进行共同培养,利用RT-PCR技术测定ALP及Runx-2 mRNA表达水平观察其分化能力。结果:流式细胞仪测定结果 显示:体外分离培养的牙周干细胞中细胞标志物CD29、CD90呈阳性,分别为88.9%与99.7%;而造血干细胞相关标 记物CD45为阴性,为0.3%;倒置显微镜结果显示:分离培养的Malassez上皮剩余细胞细胞有较大的核质比,并且不 同的细胞之间排列相对紧密,细胞整体呈“铺路石”样结构;观察组牙周组织共同培养后ALP及Runx-2 mRNA表达水 平,均高于对照组(P

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