Comparative study of stemness characteristics of mesenchymal cells from bone marrow of children and adults

被引:80
作者
Choumerianou, Despoina M. [1 ]
Martimianaki, Georgia [1 ]
Stiakaki, Eftichia [1 ]
Kalmanti, Lida [1 ]
Kalmanti, Maria [1 ]
Dimitriou, Helen [1 ]
机构
[1] Univ Crete, Sch Med, Univ Hosp Heraklion, Dept Pediat Hematol Oncol, GR-71003 Iraklion, Crete, Greece
关键词
adults; bone marrow; children; mesenchymal stromal cells; Nanog; Oct-4; telomeres; STROMAL CELLS; GENE-EXPRESSION; IN-VITRO; AGE; PLURIPOTENCY; MAINTENANCE; EXPANSION; MEDICINE;
D O I
10.3109/14653249.2010.501790
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background aims. Age-related changes that could affect the biologic features of mesenchymal stromal cells (MSC), such as a decrease in proliferation and osteoblast differentiation capacity and an increase of senescence markers and apoptosis, have been reported recently. The aim of this study was the evaluation of age-related characteristics and the correlation of age with the functional properties of MSC. Methods. The doubling time (DT), colony-forming unit-fibroblast (CFU-F) colonies and surface antigen expression of MSC isolated from bone marrow (BM) of children (C-MSC) were compared with those from adults (A-MSC). The expression of Oct-4 and Nanog transcripts and the relative telomere length were evaluated in both groups. Results. DT values were lower in C-MSC compared with A-MSC, and a higher CFU-F count was observed in children. However, the expression of Oct-4 and Nanog did not differ between C-MSC and A-MSC and was not correlated with the proliferative capacity. The telomere length was significantly higher in C-MSC compared with A-MSC. Conclusions. These data suggest that children's BM-derived MSC could be a more advantageous source of these cells for tissue engineering and cell therapy.
引用
收藏
页码:881 / 887
页数:7
相关论文
共 32 条
[1]  
Anker PSI, 2003, HAEMATOLOGICA, V88, P845
[2]   Replicative aging and gene expression in long-term cultures of human bone marrow stromal cells [J].
Banfi, A ;
Bianchi, G ;
Notaro, R ;
Luzzatto, L ;
Cancedda, R ;
Quarto, R .
TISSUE ENGINEERING, 2002, 8 (06) :901-910
[3]   Study of telomere length reveals rapid aging of human marrow stromal cells following in vitro expansion [J].
Baxter, MA ;
Wynn, RF ;
Jowitt, SN ;
Wraith, JE ;
Fairbairn, LJ ;
Bellantuono, I .
STEM CELLS, 2004, 22 (05) :675-682
[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]  
d'Adda diFagagna F., 2003, Nature, V426, P194, DOI DOI 10.1038/NATURE02118
[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 la Fuente J, 2002, BLOOD, V100, p526A
[9]   Properties and potential of bone marrow mesenchymal stromal cells from children with hematologic diseases [J].
Dimitriou, H. ;
Linardakis, E. ;
Martimianaki, G. ;
Stiakaki, E. ;
Perdikogianni, C. H. ;
Charbord, P. ;
Kalmanti, M. .
CYTOTHERAPY, 2008, 10 (02) :125-133
[10]   Are mesenchymal stromal cells from children resistant to apoptosis? [J].
Dimitriou, H. ;
Perdikogianni, Ch. ;
Martimianaki, G. ;
Choumerianou, D. M. ;
Pelagiadis, J. ;
Kalmanti, M. .
CELL PROLIFERATION, 2009, 42 (03) :276-283