TY - JOUR
T1 - Osteoclastic activity induces osteomodulin expression in osteoblasts
AU - Ninomiya, Ken
AU - Miyamoto, Takeshi
AU - Imai, Jun ichi
AU - Fujita, Nobuyuki
AU - Suzuki, Toru
AU - Iwasaki, Ryotaro
AU - Yagi, Mitsuru
AU - Watanabe, Shinya
AU - Toyama, Yoshiaki
AU - Suda, Toshio
N1 - Funding Information:
We thank Y. Sato and A. Kumakubo for technical support. T. Miyamoto was supported by a Grant-in-Aid for Young Scientists (B), Japan. T. Suda was supported by a Grant-in-Aid from Specially Promoted Research of the Ministry of Education, Science, Sports and Culture, Japan. K. Ninomiya was supported by a Grant-in-Aid from the 21st century COE Program of the Ministry of Education, Culture, Sports, Science and Technology, Japan, to Keio University. The authors have no conflicting financial interests.
PY - 2007/10/19
Y1 - 2007/10/19
N2 - Bone resorption by osteoclasts stimulates bone formation by osteoblasts. To isolate osteoblastic factors coupled with osteoclast activity, we performed microarray and cluster analysis of 8 tissues including bone, and found that among 10,490 genes, osteomodulin (OMD), an extracellular matrix keratan sulfate proteoglycan, was simultaneously induced with osteoclast-specific markers such as MMP9 and Acp5. OMD expression was detected in osteoblasts and upregulated during osteoblast maturation. OMD expression in osteoblasts was also detected immunohistochemically using a specific antibody against OMD. The immunoreactivity against OMD decreased in op/op mice, which lack functional macrophage colony stimulating factor (M-CSF) and are therefore defective in osteoclast formation, when compared to wild-type littermates. OMD expression in op/op mice was upregulated by M-CSF treatment. Since the M-CSF receptor c-Fms was not expressed in osteoblasts, it is likely that OMD is an osteoblast maturation marker that is induced by osteoclast activity.
AB - Bone resorption by osteoclasts stimulates bone formation by osteoblasts. To isolate osteoblastic factors coupled with osteoclast activity, we performed microarray and cluster analysis of 8 tissues including bone, and found that among 10,490 genes, osteomodulin (OMD), an extracellular matrix keratan sulfate proteoglycan, was simultaneously induced with osteoclast-specific markers such as MMP9 and Acp5. OMD expression was detected in osteoblasts and upregulated during osteoblast maturation. OMD expression in osteoblasts was also detected immunohistochemically using a specific antibody against OMD. The immunoreactivity against OMD decreased in op/op mice, which lack functional macrophage colony stimulating factor (M-CSF) and are therefore defective in osteoclast formation, when compared to wild-type littermates. OMD expression in op/op mice was upregulated by M-CSF treatment. Since the M-CSF receptor c-Fms was not expressed in osteoblasts, it is likely that OMD is an osteoblast maturation marker that is induced by osteoclast activity.
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U2 - 10.1016/j.bbrc.2007.07.193
DO - 10.1016/j.bbrc.2007.07.193
M3 - Article
C2 - 17714690
AN - SCOPUS:34548232692
VL - 362
SP - 460
EP - 466
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
SN - 0006-291X
IS - 2
ER -