Human gingival fibroblasts: Isolation, characterization, and evaluation of CD146 expression

被引:19
|
作者
Diar-Bakirly, Samira [1 ]
El-Bialy, Tarek [2 ]
机构
[1] Mohammed Bin Rashid Univ Med & Hlth Sci, Fac Med & Dent, Univ Alberta, Dubai, U Arab Emirates
[2] Univ Alberta, Fac Med & Dent, Katz Grp Ctr Pharm & Hlth Res 020D 7, Edmonton, AB, Canada
关键词
Gingival fibroblasts; CD146; Mesenchymal stem cells; MESENCHYMAL STEM-CELLS; HETEROGENEITY;
D O I
10.1016/j.sjbs.2021.01.053
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gingival fibroblasts (GFs) that exhibit adult stem cell-like characteristics are known as gingival mesenchymal stem cells (GMSCs). Specific mesenchymal stem cell (MSC) markers have not been identified to distinguish GMSCs from GFs. Recently, the cell surface molecule known as cluster of differentiation (CD) 146 has been identified as a potential MSC surface marker. In the present study, we investigated the differentiation potential of GMSCs based on CD146 expression. GFs were isolated by two techniques: tissue explants or enzymatic digestion. GFs were cultured and expanded then magnetically sorted according to CD146 expression. CD146(low) and CD146(high) cells were collected, expanded, and then tested for stem cell markers by flow cytometry as well as osteogenic and chondrogenic differentiation potential. The differentiation of these cells was analyzed after 21 days using histology, immunofluorescence, real-time quantitative PCR (qPCR), and glycosaminoglycan (GAG) to DNA ratio (GAG/DNA) assays. Positive histological staining indicated osteogenic differentiation of all groups regardless of the isolation techniques utilized. However, none of the groups demonstrated chondrogenic differentiation, confirmed by the lack of collagen type II in the extracellular matrix (ECM) of GF aggregates. Our data suggest that identification of gingival stem cells based solely on CD146 is not sufficient to properly carry out translational research using gingival fibroblasts for novel therapeutic methods of treating oral disease. (C) 2021 The Author(s). Published by Elsevier B.V.
引用
收藏
页码:2518 / 2526
页数:9
相关论文
共 50 条
  • [1] CD146 expression in human preimplantation blastocyst.
    Wang, H
    Wen, Y
    Mooney, S
    Behr, B
    Polan, ML
    FERTILITY AND STERILITY, 2001, 76 (03) : S203 - S203
  • [2] Differential expression of drug resistance genes in CD146 positive dental pulp derived stem cells and CD146 negative fibroblasts
    Tavangar, Maryam S.
    Attar, Armin
    Razmkhah, Mahboobeh
    Hosseini, Seyed-Mojtaba
    Hosseini, Ahmad
    Monabati, Ahmad
    Shafiei, Fereshteh
    CLINICAL AND EXPERIMENTAL DENTAL RESEARCH, 2020, 6 (04): : 448 - 456
  • [3] Characterization of CD146 expression on peripheral blood lymphocytes.
    Elshal, M
    Khan, S
    Solomon, M
    McCoy, JP
    CYTOMETRY PART B-CLINICAL CYTOMETRY, 2004, 62B (01): : 62 - 63
  • [5] Expression of MUC18 (CD146) in human choroidal melanomas
    Madigan, M. C.
    Sharma, V.
    Lai, K.
    Jager, M. J.
    Conway, R. M.
    EJC SUPPLEMENTS, 2006, 4 (06): : 31 - 31
  • [6] Different expression of CD146 in human normal and osteosarcoma cell lines
    Schiano, Concetta
    Grimaldi, Vincenzo
    Casamassimi, Amelia
    Infante, Teresa
    Esposito, Alessandra
    Giovane, Alfonso
    Napoli, Claudio
    MEDICAL ONCOLOGY, 2012, 29 (04) : 2998 - 3002
  • [7] Different expression of CD146 in human normal and osteosarcoma cell lines
    Concetta Schiano
    Vincenzo Grimaldi
    Amelia Casamassimi
    Teresa Infante
    Alessandra Esposito
    Alfonso Giovane
    Claudio Napoli
    Medical Oncology, 2012, 29 : 2998 - 3002
  • [8] CD146 Expression in Pleural and Peritoneal Mesothelioma
    Lagana, S. M.
    Taub, R. N.
    Borczuk, A. C.
    MODERN PATHOLOGY, 2012, 25 : 481A - 481A
  • [9] CD146 Expression in Pleural and Peritoneal Mesothelioma
    Lagana, S. M.
    Taub, R. N.
    Borczuk, A. C.
    LABORATORY INVESTIGATION, 2012, 92 : 481A - 481A
  • [10] PTEN and CD146 expression in endometrioid adenocarcinoma
    Huang, Q.
    He, Y.
    Cao, X.
    Yi, C.
    EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY, 2020, 41 (03) : 439 - 443