Characterization and expression analysis of mesenchymal stem cells from human bone marrow and adipose tissue

被引:732
作者
Lee, RH
Kim, B
Choi, I
Kim, H
Choi, HS
Suh, K
Bae, YC
Jung, JS
机构
[1] Pusan Natl Univ, Coll Med, Dept Physiol, Pusan 602739, South Korea
[2] Pohang Univ Sci & Technol, Div Mol & Life Sci, Pohang, South Korea
[3] Pusan Natl Univ, Coll Med, Dept Orthopaed Surg, Pusan 602739, South Korea
[4] Pusan Natl Univ, Coll Med, Dept Plast Surg, Pusan 602739, South Korea
[5] Pusan Natl Univ, Inst Med Res, Pusan 602739, South Korea
关键词
mesenchymal stem cells; bone marrow stromal cells; adipose tissue-derived stromal cells; tissue engineering; microarray analysis;
D O I
10.1159/000080341
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human mesenchymal stem cells (MSC), that have been reported to be present in bone marrow, adipose tissues, dermis, muscles and peripheral blood, have the potential to differentiate along different lineages including those forming bone, cartilage, fat, muscle and neuron. This differentiation potential makes MSC excellent candidates for cell-based tissue engineering. In this study, we have examined phenotypes and gene expression profile of the human adipose tissue-derived stromal cells (ATSC) in the undifferentiated states, and compared with that of bone marrow stromal cells (BMSC). ATSC were enzymatically released from adipose tissues from adult human donors and were expanded in monolayer with serial passages at confluence. BMSC were harvested from the metaphysis of adult human femur. Flowcytometric analysis showed that ATSC have a marker expression that is similar to that of BMSC. ATSC expressed CD29, CD44, CD90, CD105 and were absent for HLA-DR and c-kit expression. Under appropriate culture conditions, MSC were induced to differentiate to the osteoblast, adipocyte, and chondrogenic lineages. ATSC were superior to BMSC in respect to maintenance of proliferating ability, and microarray analysis of gene expression revealed differentially expressed genes between ATSC and BMSC. The proliferating ability and differentiation potential of ATSC were variable according to the culture condition. The similarities of the phenotypes and the gene expression profiles between ATSC and BMSC could have broad implications for human tissue engineering. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:311 / 324
页数:14
相关论文
共 46 条
[31]  
Preece A, 1972, MANUAL HISTOLOGIC TE
[32]  
Prockop DJ, 1998, J CELL BIOCHEM, P284, DOI 10.1002/(SICI)1097-4644(1998)72:30/31+<284::AID-JCB34>3.0.CO
[33]  
2-I
[34]   Use of real-time quantitative PCR to validate the results of cDNA array and differential display PCR technologies [J].
Rajeevan, MS ;
Ranamukhaarachchi, DG ;
Vernon, SD ;
Unger, ER .
METHODS, 2001, 25 (04) :443-451
[35]   Neurogenic differentiation of murine and human adipose-derived stromal cells [J].
Safford, KM ;
Hicok, KC ;
Safford, SD ;
Halvorsen, YDC ;
Wilkison, WO ;
Gimble, JM ;
Rice, HE .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 294 (02) :371-379
[36]   Expansion of human adult stem cells from bone marrow stroma: Conditions that maximize the yields of early progenitors and evaluate their quality [J].
Sekiya, I ;
Larson, BL ;
Smith, JR ;
Pochampally, R ;
Cui, JG ;
Prockop, DJ .
STEM CELLS, 2002, 20 (06) :530-541
[37]   CELL CONDENSATION IN CHONDROGENIC DIFFERENTIATION [J].
TACCHETTI, C ;
TAVELLA, S ;
DOZIN, B ;
QUARTO, R ;
ROBINO, G ;
CANCEDDA, R .
EXPERIMENTAL CELL RESEARCH, 1992, 200 (01) :26-33
[38]   The coronary delivery of marrow stromal cells for myocardial regeneration: Pathophysiologic and therapeutic implications [J].
Wang, JS ;
Shum-Tim, D ;
Chedrawy, E ;
Chiu, RCJ .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2001, 122 (04) :699-705
[39]   Gene expression profile of mouse bone marrow stromal cells determined by cDNA microarray analysis [J].
Wieczorek, G ;
Steinhoff, C ;
Schulz, R ;
Scheller, M ;
Vingron, M ;
Ropers, HH ;
Nuber, UA .
CELL AND TISSUE RESEARCH, 2003, 311 (02) :227-237
[40]  
Woodbury D, 2000, J NEUROSCI RES, V61, P364, DOI 10.1002/1097-4547(20000815)61:4<364::AID-JNR2>3.3.CO