Comparison of human stem cells derived from various mesenchymal tissues - Superiority of synovium as a cell source

被引:1119
作者
Sakaguchi, Y [1 ]
Sekiya, I [1 ]
Yagishita, K [1 ]
Muneta, T [1 ]
机构
[1] Tokyo Med & Dent Univ, Grad Sch, Sect Orthoped Surg, Div Matrix,Bunkyo Ku, Tokyo 1138519, Japan
来源
ARTHRITIS AND RHEUMATISM | 2005年 / 52卷 / 08期
关键词
D O I
10.1002/art.21212
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To compare the properties of human mesenchymal stem cells (MSCs) isolated from bone marrow, synovium, periosteum, skeletal muscle, and adipose tissue. Methods. Human mesenchymal tissues were obtained from 8 donors during knee surgery for ligament injury. After collagenase digestion or gradient-density separation, nucleated cells were plated at an appropriate density for expansion at the maximum rate without colony-to-colony contact. Yield, expandability, differentiation potential, and epitope profile were compared among MSCs from the 5 different tissue sources. Results. Colony number per 10(3) nucleated cells was lower, and cell number per colony was higher, in bone marrow than in other mesenchymal tissues. When the cells were replated at low density every 14 days, bone marrow-, synovium-, and periosteum-derived cells retained their proliferation ability even at passage 10. In chondrogenesis studies in which the cells were pelleted and cultured in vitro, pellets from bone marrow-, synovium-, and periosteum-derived cells were shown to be larger and stained more extensively for cartilage matrix. Synovium-derived cells, in particular, had the greatest ability for chondrogenesis. In adipogenesis experiments, the frequency of oil red O-positive colonies was highest in synovium- and adipose tissue-derived cells. In studies of osteogenesis, the rate of alizarin red-positive colonies was highest in bone marrow-, synovium-, and periosteum-derived cells. For epitope profiling, 15 surface antigens were measured. Most appeared to have similar epitope profiles irrespective of cell source. Conclusion. Our findings indicate that there are significant differences in MSC properties according to tissue source, beyond donor and experimental variation. Superiority of synovium as a potential source of MSCs for clinical applications was demonstrated.
引用
收藏
页码:2521 / 2529
页数:9
相关论文
共 42 条
[1]   Adult mesenchymal stem cells: characterization, differentiation, and application in cell and gene therapy [J].
Baksh, D ;
Song, L ;
Tuan, RS .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2004, 8 (03) :301-316
[2]   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
[3]   SYNOVIAL REGENERATION AND ARTICULAR-CARTILAGE CHANGES AFTER SYNOVECTOMY IN NORMAL AND STEROID-TREATED RABBITS [J].
BENTLEY, G ;
KREUTNER, A ;
FERGUSON, AB .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1975, 57 (04) :454-462
[4]  
CAMPBELL WG, 1971, LAB INVEST, V24, P404
[5]   Muscle stem cells differentiate into haematopoietic lineages but retain myogenic potential [J].
Cao, BH ;
Zheng, B ;
Jankowski, RJ ;
Kimura, S ;
Ikezawa, M ;
Deasy, B ;
Cummins, J ;
Epperly, M ;
Qu-Petersen, Z ;
Huard, J .
NATURE CELL BIOLOGY, 2003, 5 (07) :640-646
[6]   Rapid expansion of recycling stem cells in cultures of plastic-adherent cells from human bone marrow [J].
Colter, DC ;
Class, R ;
DiGirolamo, CM ;
Prockop, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3213-3218
[7]   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
[8]   Skeletal muscle repair by adult human mesenchymal stem cells from synovial membrane [J].
De Bari, C ;
Dell'Accio, F ;
Vandenabeele, F ;
Vermeesch, JR ;
Raymackcrs, JM ;
Luyten, FP .
JOURNAL OF CELL BIOLOGY, 2003, 160 (06) :909-918
[9]  
De Bari C, 2001, ARTHRITIS RHEUM-US, V44, P1928, DOI 10.1002/1529-0131(200108)44:8<1928::AID-ART331>3.0.CO
[10]  
2-P