Phenotypic and Functional Characterization of Mesenchymal Stem/Multipotent Stromal Cells From Decidua Parietalis of Human Term Placenta

被引:37
|
作者
Abumaree, Mohamed H. [1 ,2 ]
Abomaray, F. M. [2 ,3 ,4 ]
Alshehri, N. A. [2 ]
Almutairi, A. [5 ]
AlAskar, A. S. [2 ]
Kalionis, B. [6 ,7 ]
Al Jumah, M. A. [2 ]
机构
[1] King Saud Bin Abdulaziz Univ Hlth Sci, Coll Sci & Hlth Profess, Riyadh, Saudi Arabia
[2] King Abdullah Int Med Res Ctr, Riyadh, Saudi Arabia
[3] Karolinska Inst, Div Obstet & Gynecol, Dept Clin Sci Intervent & Technol, Stockholm, Sweden
[4] Karolinska Inst, Ctr Hematol & Regenerat Med, Stockholm, Sweden
[5] King Saud Bin Abdulaziz Univ Hlth Sci, Coll Appl Med Sci, Riyadh, Saudi Arabia
[6] Univ Melbourne, Dept Obstet & Gynaecol, Parkville, Vic, Australia
[7] Royal Womens Hosp, Dept Perinatal Med, Pregnancy Res Ctr, Parkville, Vic, Australia
关键词
placenta; decidua parietalis mesenchymal stem cells; proliferation; migration; HUMAN BONE-MARROW; STEM-CELLS; CHEMOKINE RECEPTORS; ADHESION MOLECULES; AMNIOTIC-FLUID; VASCULAR NICHE; GROWTH-FACTOR; FETAL; DIFFERENTIATION; STIMULATION;
D O I
10.1177/1933719116632924
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Mesenchymal stem/multipotent stromal cells (MSCs) from the human placenta show stem cell-like properties useful for regenerative medicine. Previously, we reported that MSCs isolated from the fetal part of human term placentae have characteristics, which make them a potential candidate for regenerative medicine. In this study, we characterized MSC isolated from the maternal part of human term placenta. The MSCs were isolated from the decidua parietalis (DPMSCs) of human placenta using a digestion method and characterized by colony-forming unit assay and the expression of MSC markers by flow cytometry technique. In addition, DPMSC differentiation into the 3 mesenchymal lineages was also performed. Moreover, the gene and protein expression profiles of DPMSCs were identified by real-time polymerase chain reaction and flow cytometry techniques, respectively. Furthermore, proteins secreted by DPMSCs were detected by sandwich enzyme-linked immunosorbent assays. Finally, the proliferation and migration potentials of DPMSCs were also determined. The DPMSCs were positive for MSC markers and negative for hematopoietic and endothelial markers, as well as costimulatory molecules and HLA-DR. Functionally, DPMSCs formed colonies and differentiated into chondrocytes, osteocytes, and adipocytes. In addition, they proliferated and migrated in response to different stimuli. Finally, they expressed and secreted many biological and immunological factors with multiple functions. Here, we carry out an extensive characterization of DPMSCs of human placenta. We report that these cells express and secrete a wide range of molecules with multiple functions, and therefore, we suggest that these cells could be an attractive candidate for cell-based therapy.
引用
收藏
页码:1193 / 1207
页数:15
相关论文
共 50 条
  • [1] Phenotypic and Functional Characterization of Mesenchymal Stem/Multipotent Stromal Cells From Decidua Parietalis of Human Term Placenta
    Mohamed H. Abumaree
    F. M. Abomaray
    N. A. Alshehri
    A. Almutairi
    A. S. AlAskar
    B. Kalionis
    M. A. Al Jumah
    Reproductive Sciences, 2016, 23 : 1193 - 1207
  • [2] Phenotypic and Functional Characterization of Mesenchymal Stem/Multipotent Stromal Cells from Decidua Basalis of Human Term Placenta
    Abomaray, F. M.
    Al Jumah, M. A.
    Alsaad, K. O.
    Jawdat, D.
    Al Khaldi, A.
    AlAskar, A. S.
    Al Harthy, S.
    Al Subayyil, A. M.
    Khatlani, T.
    Alawad, A. O.
    Alkushi, A.
    Kalionis, B.
    Abumaree, M. H.
    STEM CELLS INTERNATIONAL, 2016, 2016
  • [3] Phenotypic and Functional Characterization of Mesenchymal Stem Cells from Chorionic Villi of Human Term Placenta
    Abumaree, M. H.
    Al Jumah, M. A.
    Kalionis, B.
    Jawdat, D.
    Al Khaldi, A.
    AlTalabani, A. A.
    Knawy, B. A.
    STEM CELL REVIEWS AND REPORTS, 2013, 9 (01) : 16 - 31
  • [4] Cancer Conditioned Medium Modulates Functional and Phenotypic Properties of Human Decidua Parietalis Mesenchymal Stem/Stromal Cells
    Bahattab, E.
    Khatlani, T.
    Abomaray, F. M.
    Messaoudi, S. A.
    Abumaree, M. H.
    TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2019, 16 (06) : 615 - 630
  • [5] Cancer Conditioned Medium Modulates Functional and Phenotypic Properties of Human Decidua Parietalis Mesenchymal Stem/Stromal Cells
    E. Bahattab
    T. Khatlani
    F. M. Abomaray
    S. A. Messaoudi
    M. H. Abumaree
    Tissue Engineering and Regenerative Medicine, 2019, 16 : 615 - 630
  • [6] Mesenchymal Stem/Multipotent Stromal Cells from Human Decidua Basalis Reduce Endothelial Cell Activation
    Alshabibi, Manal A.
    Al Huqail, Al Joharah
    Khatlani, Tanvir
    Abomaray, Fawaz M.
    Alaskar, Ahmed S.
    Alawad, Abdullah O.
    Kalionis, Bill
    Abumaree, Mohamed Hassan
    STEM CELLS AND DEVELOPMENT, 2017, 26 (18) : 1355 - 1373
  • [7] Phenotypic and Functional Responses of Human Decidua Basalis Mesenchymal Stem/Stromal Cells to Lipopolysaccharide of Gram-Negative Bacteria
    Alshareef, Ghofran Hasan
    Mohammed, Afrah E.
    Abumaree, Mohammed
    Basmaeil, Yasser S.
    STEM CELLS AND CLONING-ADVANCES AND APPLICATIONS, 2021, 14 : 51 - 69
  • [8] Phenotypic and Functional Characterization of Mesenchymal Stem Cells from Chorionic Villi of Human Term Placenta
    M. H. Abumaree
    M. A. Al Jumah
    B. Kalionis
    D. Jawdat
    A. Al Khaldi
    A. A. AlTalabani
    B. A. Knawy
    Stem Cell Reviews and Reports, 2013, 9 : 16 - 31
  • [9] Characterization of the interaction between human decidua parietalis mesenchymal stem/stromal cells and natural killer cells
    Abumaree, M. H.
    Bahattab, E.
    Alsadoun, A.
    Al Dosaimani, A.
    Abomaray, F. M.
    Khatlani, T.
    Kalionis, B.
    El-Muzaini, M. F.
    Alawad, A. O.
    AlAskar, A. S.
    STEM CELL RESEARCH & THERAPY, 2018, 9
  • [10] Characteristics of Multipotent Mesenchymal Stromal Cells from Human Terminal Placenta
    Rylova, Yu. V.
    Milovanova, N. V.
    Gordeeva, M. N.
    Savilova, A. M.
    BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE, 2015, 159 (02) : 253 - 257