Comparison of Immunological Characteristics of Mesenchymal Stem Cells from the Periodontal Ligament, Umbilical Cord, an t Adipose Tissue

被引:97
作者
Kim, Jin-Hee [1 ]
Jo, Chris H. [2 ]
Kim, Hang-Rae [3 ]
Hwang, Young-il [3 ]
机构
[1] Cheongju Univ, Coll Hlth Sci, Dept Biomed Lab Sci, Chengju, South Korea
[2] Seoul Natl Univ, Coll Med, SMG SNU Boramae Med Ctr, Dept Orthoped Surg, Seoul, South Korea
[3] Seoul Natl Univ, Coll Med, Dept Anat & Cell Biol, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
MARROW STROMAL CELLS; HUMAN BONE-MARROW; IN-VITRO; IMMUNE; DIFFERENTIATION; PROLIFERATION; RESPONSES; IMMUNOGENICITY; SUPPRESSION; LYMPHOCYTE;
D O I
10.1155/2018/8429042
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal stem cells (MSCs) are of therapeutic importance in the fields of regenerative medicine and immunological diseases. Accordingly, studies evaluating MSCs for clinical applications are increasing. In this study, we characterized MSCs from the periodontal ligament, umbilical cord (UC-MSCs), and adipose tissue, which were relatively easy to obtain with limited ethical concerns regarding their acquisition, and compared their immunological characteristics. Among MSCs isolated from the three different tissues, UC-MSCs grew the fastest in vitro. The three types of MSCs were shown to inhibit proliferation of activated peripheral blood mononuclear cells (PBMCs) to a similar degree, via the indoleamine 2,3-dioxygenase and cyclooxygenase-2 pathways. They were also shown to inhibit the proliferation of PBMCs using HLA-G, which was most prominent in UC-MSCs. Unlike the other two types of MSCs, UC-MSCs showed minimal expression of HLA-DR after activation, suggesting that they pose minimal risk of initiating an allogeneic immune response when administered in vivo. These characteristics, the ease of collection, and the minimal ethical concerns regarding their use suggest UC-MSCs to be suitable MSC therapeutic candidates.
引用
收藏
页数:12
相关论文
共 54 条
[1]   Human mesenchymal stem cells modulate allogeneic immune cell responses [J].
Aggarwal, S ;
Pittenger, MF .
BLOOD, 2005, 105 (04) :1815-1822
[2]   Protein synthesis and secretion in human mesenchymal cells derived from bone marrow, adipose tissue and Wharton's jelly [J].
Amable, Paola Romina ;
Telles Teixeira, Marcus Vinicius ;
Vieira Carias, Rosana Bizon ;
Granjeiro, Jose Mauro ;
Borojevic, Radovan .
STEM CELL RESEARCH & THERAPY, 2014, 5
[3]   Murine bone marrow stromal progenitor cells elicit an in vivo cellular and humoral alloimmune response [J].
Badillo, Andrea T. ;
Beggs, Kirstin J. ;
Javazon, Elisabeth H. ;
Tebbets, Jessica C. ;
Flake, Alan W. .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2007, 13 (04) :412-422
[4]   Studying the immunosuppressive role of indoleamine 2,3-dioxygenase:: tryptophan metabolites suppress rat allogeneic T-cell responses in vitro and in vivo [J].
Bauer, TM ;
Jiga, LP ;
Chuang, JJ ;
Randazzo, M ;
Opelz, G ;
Terness, P .
TRANSPLANT INTERNATIONAL, 2005, 18 (01) :95-100
[5]   HLA-G molecules: from maternal-fetal tolerance to tissue acceptance [J].
Carosella, Edgardo D. ;
Moreau, Philippe ;
Le Maoult, Joel ;
Le Discorde, Magali ;
Dausset, Jean ;
Rouas-Freiss, Nathalie .
ADVANCES IN IMMUNOLOGY, VOL 81, 2003, 81 :199-+
[6]  
Consentius C, 2015, REGEN MED, V10, P305, DOI [10.2217/RME.15.14, 10.2217/rme.15.14]
[7]   Age-related osteogenic potential of mesenchymal stromal stem cells from human vertebral bone marrow [J].
D'Ippolito, G ;
Schiller, PC ;
Ricordi, C ;
Roos, BA ;
Howard, GA .
JOURNAL OF BONE AND MINERAL RESEARCH, 1999, 14 (07) :1115-1122
[8]  
De Miguel MP, 2012, CURR MOL MED, V12, P574
[9]   Human bone marrow stromal cells suppress T-lymphocyte proliferation induced by cellular or nonspecific mitogenic stimuli [J].
Di Nicola, M ;
Carlo-Stella, C ;
Magni, M ;
Milanesi, M ;
Longoni, PD ;
Matteucci, P ;
Grisanti, S ;
Gianni, AM .
BLOOD, 2002, 99 (10) :3838-3843
[10]   Characterization of HLA-G and Related Immunosuppressive Effects in Human Umbilical Cord Stroma-Derived Stem Cells [J].
Ding, Dah-Ching ;
Chou, Hsiang-Lan ;
Chang, Yu-Hsun ;
Hung, Wei-Ting ;
Liu, Hwan-Wun ;
Che, Tang-Yuan .
CELL TRANSPLANTATION, 2016, 25 (02) :217-228