Comparison of human dental pulp and bone marrow stromal stem cells by cDNA microarray analysis

被引:304
作者
Shi, S [1 ]
Robey, PG [1 ]
Gronthos, S [1 ]
机构
[1] NIDCR, Craniofacial & Skeletal Dis Branch, NIH, Bethesda, MD 20892 USA
关键词
dental pulp stem cells (DPSCs); bone marrow stromal stem cells (BMSSCs) cDNA microarray; osteohlast; odontoblast;
D O I
10.1016/S8756-3282(01)00612-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We compared the gene expression profiles of human dental pulp stern cells (DPSCs) and bone marrow stromal stern cells (BMSSCs) as representative populations of odontoprogenitor and osteoprogenitor cells, respectively. Total RNA from primary cultures was reverse-transcribed to generate cDNA probes and then hybridized with the Research Genetics human gene microarray filter GF211. The microarrays were analyzed using the PATHWAYS software package. Human DPSCs and BMSSCs were found to have a similar level of gene expression for more than 4000 known human genes. A few differentially expressed genes, including collagen type XVIII alpha1, insulin-like growth factor-2 (IGF-2), discordin domain tyrosine kinase 2, NAD(P)H menadione oxidoreductase, homolog 2 of Drosophila large disk, and cyclin-dependent kinase 6 were highly expressed in DPSCs, whereas insulin-like growth factor binding protein-7 (IGFBP-7), and collagen type I alpha2 were more highly expressed in BMSSCs. Furthermore, we confirmed the differential expression of these genes by semiquantitative polymerase chain reaction (PCR) and northern blot hybridization. The protein expression patterns for both IGF-2 and IGFBP-7 correlated with the differential mRNA levels seen between DPSCs and BMSSCs. This report describes the gene expression patterns of two distinct precursor populations associated with mineralized tissue, and provides a basis for further characterization of the functional roles for many of these genes in the development of dentin and bone. (C) 2001 by Elsevier Science Inc. All rights reserved.
引用
收藏
页码:532 / 539
页数:8
相关论文
共 73 条
[1]  
ALVES F, 1995, ONCOGENE, V10, P609
[2]   Zinc-binding of endostatin is essential for its antiangiogenic activity [J].
Boehm, T ;
O'Reilly, MS ;
Keough, K ;
Shiloach, J ;
Shapiro, R ;
Folkman, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 252 (01) :190-194
[3]   Matrix proteins and mineralization: An overview [J].
Boskey, AL .
CONNECTIVE TISSUE RESEARCH, 1996, 35 (1-4) :357-363
[4]   Options available - from start to finish - for obtaining expression data by microarray [J].
Bowtell, DDL .
NATURE GENETICS, 1999, 21 (Suppl 1) :25-32
[5]   Exploring the new world of the genome with DNA microarrays [J].
Brown, PO ;
Botstein, D .
NATURE GENETICS, 1999, 21 (Suppl 1) :33-37
[6]  
Butler WT, 1997, CIBA F SYMP, V205, P107
[7]  
BUTLER WT, 1995, INT J DEV BIOL, V39, P169
[8]   EXPRESSION OF THE C-FOS PROTO ONCOGENE IN BONE, CARTILAGE AND TOOTH FORMING TISSUES DURING MOUSE DEVELOPMENT [J].
CAUBET, JF ;
BERNAUDIN, JF .
BIOLOGY OF THE CELL, 1988, 64 (01) :101-104
[9]  
Chen YP, 1996, DEVELOPMENT, V122, P3035
[10]  
D'Souza RN, 1999, DEVELOPMENT, V126, P2911