Hakki Sema S, Turaç Gizem, Bozkurt S Buket, Kayis Seyit Ali, Hakki Erdogan E, Şahin Eren, Subaşı Cansu, Karaoz Erdal
Department of Periodontology, Faculty of Dentistry, Selcuk University, Konya, Turkey.
Cells Tissues Organs. 2017;204(5-6):228-240. doi: 10.1159/000478998. Epub 2017 Aug 26.
The purpose of this study was to compare the proliferation and differentiation potential of mesenchymal stem cells (MSCs) derived from palatal adipose tissue (PAT) and lipoaspirated adipose tissue (LAT).
PATs were obtained from 2 healthy female patients undergoing surgery for gingival recession, and LATs were obtained from 2 healthy female patients undergoing plastic surgery. LAT- and PAT-derived MSCs were confirmed by flow cytometry using MSC-specific surface markers. The multilineage differentiation capacity of the MSCs was analyzed. The expression of immunophenotyping, embryonic, and differentiation markers was compared between both MSC lines. The proliferation of PAT- and LAT-MSCs was evaluated using a real-time cell analyzer, and telomerase activity was determined using an ELISA-based TRAP assay. Stem cells isolated from PAT and LAT were analyzed by real-time PCR and whole genome array analysis.
The cells isolated from PAT had MSC characteristics. In addition, PAT-MSCs had significantly higher alkaline phosphatase activity and osteogenic potential than LAT-MSCs. Although the proliferation and telomerase activities of LAT-MSCs were higher than those of PAT-MSCs, the difference was not statistically significant. The level of embryonic stem cell markers (Oct4 and Nanog) was higher in LAT-MSCs than in PAT-MSCs. The whole genome array analysis demonstrated that 255 gene sequences were differentially expressed, with more than a twofold change in expression.
This is the first comparative analysis of the isolation and characterization of MSCs from PAT and LAT. PAT is an accessible source of MSCs, which could be used in periodontal and craniofacial tissue engineering.
本研究旨在比较腭部脂肪组织(PAT)和抽脂脂肪组织(LAT)来源的间充质干细胞(MSC)的增殖和分化潜能。
从2例接受牙龈退缩手术的健康女性患者获取PAT,从2例接受整形手术的健康女性患者获取LAT。使用MSC特异性表面标志物通过流式细胞术确认LAT和PAT来源的MSC。分析MSC的多向分化能力。比较两种MSC系之间免疫表型、胚胎和分化标志物的表达。使用实时细胞分析仪评估PAT和LAT-MSC的增殖,并使用基于ELISA的端粒酶重复扩增法(TRAP)测定端粒酶活性。通过实时PCR和全基因组芯片分析对从PAT和LAT分离的干细胞进行分析。
从PAT分离的细胞具有MSC特征。此外,PAT-MSC的碱性磷酸酶活性和成骨潜能明显高于LAT-MSC。虽然LAT-MSC的增殖和端粒酶活性高于PAT-MSC,但差异无统计学意义。LAT-MSC中胚胎干细胞标志物(Oct4和Nanog)的水平高于PAT-MSC。全基因组芯片分析表明,有255个基因序列差异表达,表达变化超过两倍。
这是首次对从PAT和LAT分离和鉴定MSC进行的比较分析。PAT是一种可获取的MSC来源,可用于牙周和颅面组织工程。