Comparison of Different Sources of Mesenchymal Stem Cells: Palatal versus Lipoaspirated Adipose Tissue

被引:13
|
作者
Hakki, Sema S. [1 ,2 ]
Turac, Gizem
Bozkurt, S. Buket [2 ]
Kayis, Seyit Ali [4 ]
Hakki, Erdogan E. [3 ]
Sahin, Eren [5 ]
Subasi, Cansu [5 ]
Karaoz, Erdal [5 ,6 ]
机构
[1] Selcuk Univ, Dept Periodontol, Konya, Turkey
[2] Selcuk Univ, Res Ctr, Fac Dent, Konya, Turkey
[3] Selcuk Univ, Mol Genet & Biotechnol Labs, Dept Soil Sci & Plant Nutr, Fac Agr, Konya, Turkey
[4] Karabuk Univ, Fac Med, Dept Biostat, Karabuk, Turkey
[5] Istinye Univ, Liv Hosp, Ctr Regenerat Med & Stem Cell Res & Mfg LivMedCel, Istanbul, Turkey
[6] Istinye Univ, Fac Med, Dept Histol & Embryol, Istanbul, Turkey
关键词
Adipose tissue; Mesenchymal stem cells; Palatal adipose tissue; Lipoaspiration; Regenerative therapies; OSTEOGENIC DIFFERENTIATION; BONE-MARROW; STROMAL CELLS; IN-VITRO; TRANSLATIONAL RESEARCH; PERIODONTAL-LIGAMENT; DENTAL FOLLICLE; EXPRESSION; REGENERATION; PULP;
D O I
10.1159/000478998
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Objectives: 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). Materials and Methods: 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. Results: 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. Conclusions: 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. (C) 2017 S. Karger AG, Basel
引用
收藏
页码:228 / 240
页数:13
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