Characterization of Adult Stem/Progenitor Cell Populations From Bone Marrow in a Three-Dimensional Collagen Gel Culture System

被引:16
作者
Claros, Silvia [1 ]
Rodriguez-Losada, Noela [2 ]
Cruz, Encarnacion [3 ]
Guerado, Enrique [3 ]
Becerra, Jose [1 ,4 ]
Andrades, Jose A. [1 ]
机构
[1] Univ Malaga, Fac Sci, Dept Cell Biol Genet & Physiol, Networking Biomed Res Ctr Bioengn Biomat & Nanome, E-29071 Malaga, Spain
[2] Virgen Victoria Univ Hosp, Heart Unit, Res Lab, Malaga, Spain
[3] Hosp Costa Sol, Div Orthopaed Surg & Traumatol, Marbella, Spain
[4] Univ Malaga, BIONAND, E-29071 Malaga, Spain
关键词
Stem/progenitor cells; Three-dimensional (3D) culture; Transforming growth factor-beta 1 (TGF-beta 1); Osteogenesis; Demineralized bone matrix; MESENCHYMAL STEM-CELLS; STROMAL CELLS; ENDOTHELIAL-CELLS; PROGENITOR CELLS; FUSION PROTEIN; IN-VITRO; DIFFERENTIATION; PLURIPOTENCY; EXPRESSION; BIOLOGY;
D O I
10.3727/096368912X636939
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Stem cell transplantation therapy using mesenchymal stem cells (MSCs) is considered a useful strategy. Although MSCs are commonly isolated by exploiting their plastic adherence, several studies have suggested that there are other populations of stem and/or osteoprogenitor cells that are removed from primary culture during media replacement. Therefore, we developed a three-dimensional (3D) culture system in which adherent and nonadherent stem cells are selected and expanded. Here, we described the characterization of 3D culture-derived cell populations in vitro and the capacity of these cells to differentiate into hone and/or cartilage tissue when placed inside of demineralized bone matrix (DBM) cylinders, implanted subcutaneously into the backs of rat for 2, 4, and 8 weeks. Our results demonstrates that 3D culture cells were a heterogeneous population of uncommitted cells that express pluripotent-, hematopoietic-, mesenchymal-, and endothelial-specific markers in vitro and can undergo osteogenic differentiation in vivo.
引用
收藏
页码:2021 / 2032
页数:12
相关论文
共 57 条
[31]   Individual fates of mesenchymal stem cells in vitro [J].
Krinner, Axel ;
Hoffmann, Martin ;
Loeffler, Markus ;
Drasdo, Dirk ;
Galle, Joerg .
BMC SYSTEMS BIOLOGY, 2010, 4
[32]   A population of very small embryonic-like (VSEL) CXCR4+SSEA-1+Oct-4+ stem cells identified in adult bone marrow [J].
Kucia, M ;
Reca, R ;
Campbell, FR ;
Zuba-Surma, E ;
Majka, M ;
Ratajczak, J ;
Ratajczak, MZ .
LEUKEMIA, 2006, 20 (05) :857-869
[33]   Effect of Cell-Based VEGF Gene Therapy on Healing of a Segmental Bone Defect [J].
Li, Ru ;
Stewart, Duncan J. ;
von Schroeder, Herbert P. ;
Mackinnon, Erin S. ;
Schemitsch, Emil H. .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2009, 27 (01) :8-14
[34]   Circulating endothelial/skeletal progenitor cells for bone regeneration and healing [J].
Matsumoto, Tomoyuki ;
Kuroda, Ryosuke ;
Mifune, Yutaka ;
Kawamoto, Atsuhiko ;
Shoji, Taro ;
Miwa, Masahiko ;
Asahara, Takayuki ;
Kurosaka, Masahiro .
BONE, 2008, 43 (03) :434-439
[35]   Nonstimulated human uncommitted mesenchymal stem cells express cell markers of mesenchymal and neural lineages [J].
Minguell, JJ ;
Fierro, FA ;
Epuñan, MJ ;
Erices, AA ;
Sierralta, WD .
STEM CELLS AND DEVELOPMENT, 2005, 14 (04) :408-414
[36]   The homeoprotein Nanog is required for maintenance of pluripotency in mouse epiblast and ES cells [J].
Mitsui, K ;
Tokuzawa, Y ;
Itoh, H ;
Segawa, K ;
Murakami, M ;
Takahashi, K ;
Maruyama, M ;
Maeda, M ;
Yamanaka, S .
CELL, 2003, 113 (05) :631-642
[37]  
Nimni M.E., 1988, CLIN ORTHOP RELAT R, V234, P255
[38]   Expression of VEGFR-2 and AC133 by circulating human CD34+ cells identifies a population of functional endothelial precursors [J].
Peichev, M ;
Naiyer, AJ ;
Pereira, D ;
Zhu, ZP ;
Lane, WJ ;
Williams, M ;
Oz, MC ;
Hicklin, DJ ;
Witte, L ;
Moore, MAS ;
Rafii, S .
BLOOD, 2000, 95 (03) :952-958
[39]   Multilineage potential of adult human mesenchymal stem cells [J].
Pittenger, MF ;
Mackay, AM ;
Beck, SC ;
Jaiswal, RK ;
Douglas, R ;
Mosca, JD ;
Moorman, MA ;
Simonetti, DW ;
Craig, S ;
Marshak, DR .
SCIENCE, 1999, 284 (5411) :143-147
[40]   Vascular and haematopoietic stem cells:: Novel targets for anti-angiogenesis therapy? [J].
Rafii, S ;
Lyden, D ;
Benezra, R ;
Hattorï, K ;
Heissig, B .
NATURE REVIEWS CANCER, 2002, 2 (11) :826-835