Comparative evaluation of mesenchymal stromal cells from umbilical cord and amniotic membrane in xeno-free conditions

被引:9
作者
Mu, Yongxu [1 ,2 ]
Wu, Xiaoyun [3 ,4 ]
Hao, Zhiming [1 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Rheumatol, Xian, Shaanxi, Peoples R China
[2] Inner Mongolia Univ Sci & Technol, Affiliated Hosp 1, Baotou Med Coll, Dept Intervent Treatment, Baotou, Inner Mongolia, Peoples R China
[3] Stem Cell Med Engn & Technol Res Ctr Inner Mongol, Dept Technol, Hohhot, Inner Mongolia, Peoples R China
[4] Beijing Jingmeng Stem Cell Technol Co Ltd, Dept Res & Dev, Beijing, Peoples R China
来源
BMC CELL BIOLOGY | 2018年 / 19卷
基金
中国国家自然科学基金;
关键词
Mesenchymal stromal cells; Amnion; Umbilical cord; Platelet lysate; Characteristics; Immunomodulatory; PLATELET-RICH PLASMA; CLINICAL-GRADE PRODUCTION; STEM-CELLS; BONE-MARROW; INTERNATIONAL-SOCIETY; BLOOD; EXPANSION; GROWTH; LYSATE; DIFFERENTIATION;
D O I
10.1186/s12860-018-0178-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
BackgroundWithin the past years, umbilical cord (UC) and amniotic membrane (AM) expanded in human platelet lysate (PL) have been found to become increasingly candidate of mesenchymal stromal cells (MSCs) in preclinical and clinical studies. Different sources of MSCs have different properties, and lead to different therapeutic applications. However, the similarity and differences between the AMMSCs and UCMSCs in PL remain unclear.ResultsIn this study, we conduct a direct head-to-head comparison with regard to biological characteristics (morphology, immunophenotype, self-renewal capacity, and trilineage differentiation potential) and immunosuppression effects of AMMSCs and UCMSCs expanded in PL. Our results indicated that AMMSCs showed similar morphology, immunophenotype, proliferative capacity and colony efficiency with UCMSCs. Moreover, no significantly differences in osteogenic, chondrogenic and adipogenic differentiation potential were observed between the two types of cells. However, AMMSCs exhibited higher PGE(2) expression and IDO activity compared with UCMSCs when primed by IFN- and (or) TNF- induction, and AMMSCs showed a higher inhibitory effect on PBMCs proliferation than UCMSCs.ConclusionThe results suggest that AMMSCs expanded in PL showed similar morphology, immunophenotype, self-renewal capacity, and trilineage differentiation potential with UCMSCs. However, AMMSCs possessed superior immunosuppression effects in comparison with UCMSCs. These results suggest that AMMSCs in PL might be more suitable than UCMSCs for treatment of immune diseases. This work provides a novel insight into choosing the appropriate source of MSCs for treatment of immune diseases.
引用
收藏
页数:10
相关论文
共 41 条
[1]   Comparison of human mesenchymal stromal cells from four neonatal tissues: Amniotic membrane, chorionic membrane, placental decidua and umbilical cord [J].
Araujo, Anelise Bergmann ;
Salton, Gabrielle Dias ;
Furlan, Juliana Monteiro ;
Schneider, Natalia ;
Angeli, Melissa Helena ;
Laureano, Alvaro Macedo ;
Silla, Lucia ;
Passos, Eduardo Pandolfi ;
Paz, Ana Helena .
CYTOTHERAPY, 2017, 19 (05) :577-585
[2]   What Makes Umbilical Cord Tissue-Derived Mesenchymal Stromal Cells Superior Immunomodulators When Compared to Bone Marrow Derived Mesenchymal Stromal Cells? [J].
Barcia, R. N. ;
Santos, J. M. ;
Filipe, M. ;
Teixeira, M. ;
Martins, J. P. ;
Almeida, J. ;
Agua-Doce, A. ;
Almeida, S. C. P. ;
Varela, A. ;
Pohl, S. ;
Dittmar, K. E. J. ;
Calado, S. ;
Simoes, S. I. ;
Gaspar, M. M. ;
Cruz, M. E. M. ;
Lindenmaier, W. ;
Graca, L. ;
Cruz, H. ;
Cruz, P. E. .
STEM CELLS INTERNATIONAL, 2015, 2015
[3]   Risk of tumorigenicity in mesenchymal stromal cell-based therapies-Bridging scientific observations and regulatory viewpoints [J].
Barkholt, Lisbeth ;
Flory, Egbert ;
Jekerle, Veronika ;
Lucas-Samuel, Sophie ;
Ahnert, Peter ;
Bisset, Louise ;
Buescher, Dirk ;
Fibbe, Willem ;
Foussat, Arnaud ;
Kwa, Marcel ;
Lantz, Olivier ;
Maciulaitis, Romaldas ;
Palomaki, Tiina ;
Schneider, Christian K. ;
Sensebe, Lug ;
Tachdjian, Gerard ;
Tarte, Karin ;
Tosca, Lucie ;
Salmikangas, Paula .
CYTOTHERAPY, 2013, 15 (07) :753-759
[4]   In Vivo Therapeutic Potential of Mesenchymal Stromal Cells Depends on the Source and the Isolation Procedure [J].
Bortolotti, Francesca ;
Ukovich, Laura ;
Razban, Vahid ;
Martinelli, Valentina ;
Ruozi, Giulia ;
Pelos, Barbara ;
Dore, Franca ;
Giacca, Mauro ;
Zacchigna, Serena .
STEM CELL REPORTS, 2015, 4 (03) :332-339
[5]   Human platelet lysate allows expansion and clinical grade production of mesenchymal stromal cells from small samples of bone marrow aspirates or marrow filter washouts [J].
Capelli, C. ;
Domenghini, M. ;
Borleri, G. ;
Bellavita, P. ;
Poma, R. ;
Carobbio, A. ;
Mico, C. ;
Rambaldi, A. ;
Golay, J. ;
Introna, M. .
BONE MARROW TRANSPLANTATION, 2007, 40 (08) :785-791
[6]   Comparison of biological characteristics of mesenchymal stem cells derived from maternal-origin placenta and Wharton's jelly [J].
Chen, Gecai ;
Yue, Aihuan ;
Ruan, Zhongbao ;
Yin, Yigang ;
Wang, Ruzhu ;
Ren, Yin ;
Zhu, Li .
STEM CELL RESEARCH & THERAPY, 2015, 6
[7]   Isolation method and xeno-free culture conditions influence multipotent differentiation capacity of human Wharton's jelly-derived mesenchymal stem cells [J].
Corotchi, Maria Cristina ;
Popa, Mirel Adrian ;
Remes, Anca ;
Sima, Livia Elena ;
Gussi, Ilinca ;
Plesu, Marilena Lupu .
STEM CELL RESEARCH & THERAPY, 2013, 4
[8]   Comparison of the paracrine activity of mesenchymal stem cells derived from human umbilical cord, amniotic membrane and adipose tissue [J].
Dabrowski, Filip A. ;
Burdzinska, Anna ;
Kulesza, Agnieszka ;
Sladowska, Anna ;
Zolocinska, Aleksandra ;
Gala, Kamila ;
Paczek, Leszek ;
Wielgos, Miroslaw .
JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH, 2017, 43 (11) :1758-1768
[9]   Concise Review: Wharton's Jelly: The Rich, but Enigmatic, Source of Mesenchymal Stromal Cells [J].
Davies, John E. ;
Walker, John T. ;
Keating, Armand .
STEM CELLS TRANSLATIONAL MEDICINE, 2017, 6 (07) :1620-1630
[10]   Regulatory perspective on in vitro potency assays for human mesenchymal stromal cells used in immunotherapy [J].
De Wolf, Charlotte ;
Van De Bovenkamp, Marja ;
Hoefnagel, Marcel .
CYTOTHERAPY, 2017, 19 (07) :784-797