Clonal composition of human multipotent mesenchymal stromal cells

被引:13
作者
Bigildeev, Alexey E. [1 ]
Zhironkina, Oxana A. [1 ]
Shipounova, Irina N. [1 ]
Sats, Natalia V. [1 ]
Kotyashova, Svetlana Y. [1 ]
Drize, Nina I. [1 ]
机构
[1] Minist Hlth & Social Dev, FSBI Hematol Res Ctr, Moscow 125167, Russia
关键词
HEMATOPOIETIC STEM-CELLS; HUMAN BONE-MARROW; LENTIVIRAL VECTOR; TRANSFORMATION; CULTURES;
D O I
10.1016/j.exphem.2012.06.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multipotent mesenchymal stromal cells (MMSCs) are a heterogeneous population consisting of cells with a distinct proliferative potential. The aim of this study was to define clonal composition in MMSCs and trace the dynamics of individual clones in MMSC subpopulations with different proliferative potentials during the process of cultivation. The investigation was performed at single-cell level using genetically marked cells. Specifically, human bone marrow MMSCs were infected with a lentiviral vector-bearing marker gene. Integration site analysis was performed for clones at each passage by ligation-mediated polymerase chain reaction and Southern blot hybridization. Sibling connections between clones and clonal composition of MMSC culture at each passage were revealed. The MMSC population contained multiple, different, mainly small, clones. It was found that large long-living clones with a high, but limited proliferative potential could be detected rarely in MMSCs population. These data suggest that the human MMSC population does not fit the "stem cell" criteria, however, MMSCs may contain a subpopulation of large clones with a high proliferative potential. (C) 2012 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc.
引用
收藏
页码:847 / 856
页数:10
相关论文
共 27 条
[1]   Human bone marrow-derived mesenchymal stem cells do not undergo transformation after long-term In vitro culture and do not exhibit telomere maintenance mechanisms [J].
Bernardo, Maria Ester ;
Zaffaroni, Nadia ;
Novara, Francesca ;
Cometa, Angela Maria ;
Avanzini, Maria Antonietta ;
Moretta, Antonia ;
Montagna, Daniela ;
Maccario, Rita ;
Villa, Raffaella ;
Daidone, Maria Grazia ;
Zuffardi, Orsetta ;
Locatelli, Franco .
CANCER RESEARCH, 2007, 67 (19) :9142-9149
[2]   Lentiviral vector common integration sites in preclinical models and a clinical trial reflect a benign integration bias and not oncogenic selection [J].
Biffi, Alessandra ;
Bartholomae, Cynthia C. ;
Cesana, Daniela ;
Cartier, Natalie ;
Aubourg, Patrik ;
Ranzani, Marco ;
Cesani, Martina ;
Benedicenti, Fabrizio ;
Plati, Tiziana ;
Rubagotti, Enrico ;
Merella, Stefania ;
Capotondo, Alessia ;
Sgualdino, Jacopo ;
Zanetti, Gianluigi ;
von Kalle, Christof ;
Schmidt, Manfred ;
Naldini, Luigi ;
Montini, Eugenio .
BLOOD, 2011, 117 (20) :5332-5339
[3]   MESENCHYMAL STEM-CELLS [J].
CAPLAN, AI .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1991, 9 (05) :641-650
[4]   Mesenchymal stem cells: building blocks for molecular medicine in the 21st century [J].
Caplan, AI ;
Bruder, SP .
TRENDS IN MOLECULAR MEDICINE, 2001, 7 (06) :259-264
[5]   Study of oncogenic transformation in ex vivo expanded mesenchymal cells, from paediatric bone marrow [J].
Choumerianou, D. M. ;
Dimitriou, H. ;
Perdikogianni, C. ;
Martimianaki, G. ;
Riminucci, M. ;
Kalmanti, M. .
CELL PROLIFERATION, 2008, 41 (06) :909-922
[6]   Identification of a subpopulation of rapidly self-renewing and multipotential adult stem cells in colonies of human marrow stromal cells [J].
Colter, DC ;
Sekiya, I ;
Prockop, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (14) :7841-7845
[7]   Age-associated loss of bone marrow hematopoietic cells is reversed by GH and accompanies thymic reconstitution [J].
French, RA ;
Broussard, SR ;
Meier, WA ;
Minshall, C ;
Arkins, S ;
Zachary, JF ;
Dantzer, R ;
Kelley, KW .
ENDOCRINOLOGY, 2002, 143 (02) :690-699
[8]   Overexpression in Escherichia coli and purification of human fibroblast growth factor (FGF-2) [J].
Gasparian, M. E. ;
Elistratov, P. A. ;
Drize, N. I. ;
Nifontova, I. N. ;
Dolgikh, D. A. ;
Kirpichnikov, M. P. .
BIOCHEMISTRY-MOSCOW, 2009, 74 (02) :221-225
[9]   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
[10]   Clonal dominance of hematopoietic stem cells triggered by retroviral gene marking [J].
Kustikova, O ;
Fehse, B ;
Modlich, U ;
Yang, M ;
Düllmann, J ;
Kamino, K ;
von Neuhoff, N ;
Schlegelberger, B ;
Li, ZX ;
Baum, C .
SCIENCE, 2005, 308 (5725) :1171-1174