Ex vivo enrichment of mesenchymal cell progenitors by fibroblast growth factor 2

被引:319
作者
Bianchi, G
Banfi, A
Mastrogiacomo, M
Notaro, R
Luzzatto, L
Cancedda, R
Quarto, R
机构
[1] Univ Genoa, Lab Med Rigenerat, Dip Oncol Biol Genet, I-16132 Genoa, Italy
[2] Ctr Biotecnol Avanzate, Genoa, Italy
[3] Ist Nazl Ric Canc, I-16132 Genoa, Italy
关键词
bone marrow stromal cells; osteoprogenitors; telomeres; fibroblast growth factor 2; tissue engineering;
D O I
10.1016/S0014-4827(03)00138-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Bone marrow stromal cells, obtained from postnatal bone marrow, contain progenitors able to differentiate into several mesenchymal lineages. Their use in gene and cell therapy requires their in vitro expansion and calls for the investigation of the culture conditions required to preserve these cells as a stem compartment with high differentiative potential during their life span. Here we report that fibroblast growth factor 2 (FGF-2)-supplemented bone marrow stromal cell primary cultures display an early increase in telomere size followed by a gradual decrease, whereas in control cultures telomere length steadily decreases with increasing population doublings. Together with clonogenic culture conditions, FGF-2 supplementation prolongs the life span of bone marrow stromal cells to more than 70 doublings and maintains their differentiation potential until 50 doublings. These results suggest that FGF-2 in vitro selects for the survival of a particular subset of cells enriched in pluripotent mesenchymal precursors and is useful in obtaining a large number of cells with preserved differentiation potential for mesenchymal tissue repair. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:98 / 105
页数:8
相关论文
共 45 条
  • [1] Proliferation kinetics and differentiation potential of ex vivo expanded human bone marrow stromal cells: Implications for their use in cell therapy
    Banfi, A
    Muraglia, A
    Dozin, B
    Mastrogiacomo, M
    Cancedda, R
    Quarto, R
    [J]. EXPERIMENTAL HEMATOLOGY, 2000, 28 (06) : 707 - 715
  • [2] Replicative aging and gene expression in long-term cultures of human bone marrow stromal cells
    Banfi, A
    Bianchi, G
    Notaro, R
    Luzzatto, L
    Cancedda, R
    Quarto, R
    [J]. TISSUE ENGINEERING, 2002, 8 (06): : 901 - 910
  • [3] Bone marrow stromal stem cells: Nature, biology, and potential applications
    Bianco, P
    Riminucci, M
    Gronthos, S
    Robey, PG
    [J]. STEM CELLS, 2001, 19 (03) : 180 - 192
  • [4] Marrow stromal stem cells
    Bianco, P
    Robey, PG
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (12) : 1663 - 1668
  • [5] Bruder SP, 1997, J CELL BIOCHEM, V64, P278, DOI 10.1002/(SICI)1097-4644(199702)64:2<278::AID-JCB11>3.0.CO
  • [6] 2-F
  • [7] CASTROMALASPINA H, 1980, BLOOD, V56, P289
  • [8] Differential expression of telomerase activity in hematopoietic progenitors from adult human bone marrow
    Chiu, CP
    Dragowska, W
    Kim, NW
    Vaziri, H
    Yui, J
    Thomas, TE
    Harley, CB
    Lansdorp, PM
    [J]. STEM CELLS, 1996, 14 (02) : 239 - 248
  • [9] Rapid expansion of recycling stem cells in cultures of plastic-adherent cells from human bone marrow
    Colter, DC
    Class, R
    DiGirolamo, CM
    Prockop, DJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) : 3213 - 3218
  • [10] Identification of a subpopulation of rapidly self-renewing and multipotential adult stem cells in colonies of human marrow stromal cells
    Colter, DC
    Sekiya, I
    Prockop, DJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (14) : 7841 - 7845