TY - JOUR
T1 - Promotion of Ccn2 expression and osteoblastic differentiation by actin polymerization, which is induced by laminar fluid flow stress
AU - Honjo, Tadashi
AU - Kubota, Satoshi
AU - Kamioka, Hiroshi
AU - Sugawara, Yasuyo
AU - Ishihara, Yoshihito
AU - Yamashiro, Takashi
AU - Takigawa, Masaharu
AU - Takano-Yamamoto, Teruko
PY - 2012/12
Y1 - 2012/12
N2 - Fluid flow stress (FSS) is a major mechanical stress that induces bone remodeling upon orthodontic tooth movement, whereas CCN family protein 2 (CCN2) is a potent regenerator of bone defects. In this study, we initially evaluated the effect of laminar FSS on Ccn2 expression and investigated its mechanism in osteoblastic MC3T3-E1 cells. The Ccn2 expression was drastically induced by uniform FSS in an intensity dependent manner. Of note, the observed effect was inhibited by a Rho kinase inhibitor Y27632. Moreover, the inhibition of actin polymerization blocked the FSS-induced activation of Ccn2, whereas inducing Factin formation using cytochalasin D and jasplakinolide enhanced Ccn2 expression in the same cells. Finally, Factin formation was found to induce osteoblastic differentiation. In addition, activation of cyclic AMP-dependent kinase, which inhibits Rho signaling, abolished the effect of FSS. Collectively, these findings indicate the critical role of actin polymerization and Rho signaling in CCN2 induction and bone remodeling provoked by FSS.
AB - Fluid flow stress (FSS) is a major mechanical stress that induces bone remodeling upon orthodontic tooth movement, whereas CCN family protein 2 (CCN2) is a potent regenerator of bone defects. In this study, we initially evaluated the effect of laminar FSS on Ccn2 expression and investigated its mechanism in osteoblastic MC3T3-E1 cells. The Ccn2 expression was drastically induced by uniform FSS in an intensity dependent manner. Of note, the observed effect was inhibited by a Rho kinase inhibitor Y27632. Moreover, the inhibition of actin polymerization blocked the FSS-induced activation of Ccn2, whereas inducing Factin formation using cytochalasin D and jasplakinolide enhanced Ccn2 expression in the same cells. Finally, Factin formation was found to induce osteoblastic differentiation. In addition, activation of cyclic AMP-dependent kinase, which inhibits Rho signaling, abolished the effect of FSS. Collectively, these findings indicate the critical role of actin polymerization and Rho signaling in CCN2 induction and bone remodeling provoked by FSS.
KW - Actin polymerization
KW - CCN2
KW - CTGF
KW - Connective tissue growth factor
KW - Fluid shear stress
KW - Osteoblasts
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U2 - 10.1007/s12079-012-0177-z
DO - 10.1007/s12079-012-0177-z
M3 - Article
C2 - 22956334
AN - SCOPUS:84874105864
SN - 1873-9601
VL - 6
SP - 225
EP - 232
JO - Journal of Cell Communication and Signaling
JF - Journal of Cell Communication and Signaling
IS - 4
ER -