Rm. Locklin et al., Assessment of gene regulation by bone morphogenetic protein 2 in human marrow stromal cells using gene array technology, J BONE MIN, 16(12), 2001, pp. 2192-2204
Marrow stromal cells can differentiate into osteoblasts, adipocytes, myobla
sts, and chondrocytes. Bone morphogenetic protein 2 (BMP-2) is a potent sti
mulator of osteoblastic differentiation, and identification of the genes re
gulated by BMP-2 in these cells should provide insight into the mechanism(s
) of osteoblastic differentiation. Thus, we used a conditionally immortaliz
ed human marrow stromal cell line (hMS) and a gene expression microarray co
ntaining probes for a total of 6800 genes to compare gene expression in con
trol and BMP-2-treated cultures. A total of 51 genes showed a consistent ch
ange in messenger RNA (mRNA) frequency between two repeat experiments. Seve
nteen of these genes showed a change in expression of at least 3-fold in BM
P-2-treated cultures over control cultures. These included nuclear binding
factors (10 genes), signal transduction pathway genes (2 genes), molecular
transport (1 gene), cell surface proteins (2 genes) and growth factors (2 g
enes). Of particular interest were four of the nuclear binding factor genes
ID-1, ID-2, ID-3, and ID-4. These encode dominant negative helix-loop-heli
x (dnHLH) proteins that lack the nuclear binding domain of the basic HLH pr
oteins and thus have no transcriptional activity. They have been implicated
in blocking both myogenesis and adipogenesis. Other transcription factors
up-regulated at least 3-fold by BMP-2 included Dlx-2, HES-1, STAT1, and Jun
B. The changes in these nuclear binding factor mRNA levels were confirmed b
y real-time reverse-transcriptase-polymerase chain reaction (RT-PCR). A fur
ther three transcription factors, core binding factor beta (CBF beta), AREB
6, and SOX4, showed changes in expression of between 2- and 3-fold with BMP
-2 treatment. In summary, we have used a gene chip microarray to identify a
number of BMP-2 responsive genes in hMS cells. Thus, these studies provide
potential candidate genes that may induce osteoblastic differentiation or,
in the case of the ID proteins, block differentiation along alternate path
ways.