Characterization of mesenchymal stromal cells derived from full-term umbilical cord blood

被引:66
作者
Manca, M. F. [1 ]
Zwart, I. [2 ]
Beo, J. [1 ]
Palasingham, R. [1 ]
Jen, L-S [2 ]
Navarrete, R. [2 ]
Girdlestone, J. [1 ]
Navarrete, C. V. [1 ]
机构
[1] Natl Hlth Serv Blood & Transplant Histocompatibil, Colindale Ctr, London, England
[2] Univ London Imperial Coll Sci Technol & Med, DEpt Cellular & Mol Neurosci, London, England
关键词
differentiation; karyotype; mesenchymal stromal cells; umbilical cord blood;
D O I
10.1080/14653240701732763
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background Multipotent mesenchymal stromal cells (MSC) are of interest for their potential to repair bone and cartilage, and also their immunosuppressive properties. Umbilical cord blood (UCB) is reported to contain MSC, and therefore may be a useful source of these cells for clinical applications. Methods We evaluated protocols for isolating MSC from UCB and characterized the surface phenotype, differentiation potential and immunoregulatory properties of the cells obtained. Results Ten of 25 UCB units processed yielded MSC-like colonies, with depletion of lineage+ cells providing a higher efficiency. Only two of the cultures could be expanded satisfactorily; the remainder failed to proliferate. One culture generated transformed lines that were grossly aneuploid, had up-regulated TERT transcripts and had lost CD90 expression and the capacity to differentiate. The two propagated UCB-MSC lines were similar to those from bone marrow but were not identical to each other, with differences seen in expression of surface markers and cytoskeletal proteins. Both underwent osteogenesis, but at different rates and to different degrees, while neither generated adipocytes. When added as a third party to a mixed lymphocyte culture, both suppressed proliferation. Discussion MSC-like cells can be isolated from UCB, but at low efficiencies, and they exhibit a variety of morphologies, growth rates and differentiation potentials and can transform in culture.
引用
收藏
页码:54 / 68
页数:15
相关论文
共 50 条
[21]   The Notch pathway in ovarian carcinomas and adenomas [J].
Hopfer, O ;
Zwahlen, D ;
Fey, MF ;
Aebi, S .
BRITISH JOURNAL OF CANCER, 2005, 93 (06) :709-718
[22]   Transplantability and therapeutic effects of bone marrow-derived mesenchymal cells in children with osteogenesis imperfecta [J].
Horwitz, EM ;
Prockop, DJ ;
Fitzpatrick, LA ;
Koo, WWK ;
Gordon, PL ;
Neel, M ;
Sussman, M ;
Orchard, P ;
Marx, JC ;
Pyeritz, RE ;
Brenner, MK .
NATURE MEDICINE, 1999, 5 (03) :309-313
[23]   Clarification of the nomenclature for MSC: The international society for cellular therapy position statement [J].
Horwitz, EM ;
Le Blanc, K ;
Dominici, M ;
Mueller, I ;
Slaper-Cortenbach, I ;
Marini, FC ;
Deans, RJ ;
Krause, DS ;
Keating, A .
CYTOTHERAPY, 2005, 7 (05) :393-395
[24]   Biologic properties of mesenchymal stem cells derived from bone marrow and adipose tissue [J].
Izadpanah, Reza ;
Trygg, Cynthia ;
Patel, Bindiya ;
Kriedt, Christopher ;
Dufour, Jason ;
Gimble, Jeffery M. ;
Bunnell, Bruce A. .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2006, 99 (05) :1285-1297
[25]   Pluripotency of mesenchymal stem cells derived from adult marrow [J].
Jiang, Yuehua ;
Jahagirdar, Balkrishna N. ;
Reinhardt, R. Lee ;
Schwartz, Robert E. ;
Keene, C. Dirk ;
Ortiz-Gonzalez, Xilma R. ;
Reyes, Morayma ;
Lenvik, Todd ;
Lund, Troy ;
Blackstad, Mark ;
Du, Jingbo ;
Aldrich, Sara ;
Lisberg, Aaron ;
Low, Walter C. ;
Lergaespada, David A. ;
Verfaillie, Catherine M. .
Nature, 2002, 418 (6893) :41-49
[26]   Jagged2-expressing hematopoietic progenitors promote regulatory T cell expansion in the periphery through notch signaling [J].
Kared, Hassen ;
Adle-Biassette, Homa ;
Fois, Elena ;
Masson, Annie ;
Bach, Jean-Francois ;
Chatenoud, Lucienne ;
Schneider, Elke ;
Zavala, Flora .
IMMUNITY, 2006, 25 (05) :823-834
[27]   Isolation of mesenchymal stem cells from G-CSF-mobilized human peripheral blood using fibrin microbeads [J].
Kassis, I ;
Zangi, L ;
Rivkin, R ;
Levdansky, L ;
Samuel, S ;
Marx, G ;
Gorodetsky, R .
BONE MARROW TRANSPLANTATION, 2006, 37 (10) :967-976
[28]   Comparative analysis of mesenchymal stem cells from bone marrow, umbilical cord blood, or adipose tissue [J].
Kern, Susanne ;
Eichler, Hermann ;
Stoeve, Johannes ;
Klueter, Harald ;
Bieback, Karen .
STEM CELLS, 2006, 24 (05) :1294-1301
[29]   Fetal mesenchymal stem-cell engraftment in bone after in utero transplantation in a patient with severe osteogenesis imperfecta [J].
Le Blanc, K ;
Götherström, C ;
Ringdén, O ;
Hassan, M ;
McMahon, R ;
Horwitz, E ;
Anneren, G ;
Axelsson, O ;
Nunn, J ;
Ewald, U ;
Nordén-Lindeberg, S ;
Jansson, M ;
Dalton, A ;
Åström, E ;
Westgren, M .
TRANSPLANTATION, 2005, 79 (11) :1607-1614
[30]   Treatment of severe acute graft-versus-host disease with third party haploidentical mesenchymal stem cells [J].
Le Blanc, K ;
Rasmusson, I ;
Sundberg, B ;
Götherström, C ;
Hassan, M ;
Uzunel, M ;
Ringdén, O .
LANCET, 2004, 363 (9419) :1439-1441