Regulation of SFRP-1 Expression in the Rat Dental Follicle

References

• Cahill, D.R., and Marks, Jr., S.C. (1980). Tooth eruption: Evidence for the central role of the dental follicle. J. Oral Pathol. Med. 9:189–200.
   Web of Science ®Google Scholar
• Wise, G.E., and King, G.J. (2008). Mechanisms of tooth eruption and orthodontic tooth movement. J. Dent. Res. 87:414–434.
   PubMed Web of Science ®Google Scholar
• Wise, G.E. (2009). Cellular and molecular basis of tooth eruption. Orthod. Craniofac. Res. 12:67–73.
   PubMed Web of Science ®Google Scholar
• Marks, Jr., S.C., Cahill, D.R., and Wise, G.E. (1983). The cytology of the dental follicle and adjacent alveolar bone during tooth eruption in the dog. Am. J. Anat. 168:277–289.
   PubMedGoogle Scholar
• Wise, G.E., and Fan, W. (1989). Changes in the tartrate-resistant acid phosphatase cell population in dental follicles and bony crypts of rat molars during tooth eruption. J. Dent. Res. 68:150–156.
   PubMed Web of Science ®Google Scholar
• Wise, G.E., Lin, F., and Zhao, L. (1995). Transcription and translation of CSF-1 in the dental follicle. J. Dent. Res. 74:1551–1557.
   PubMed Web of Science ®Google Scholar
• Que, B.G., and Wise, G.E. (1997). Colony-stimulating factor-1 and monocyte chemotactic protein-1 chemotaxis for monocytes in the rat dental follicle. Arch. Oral Biol. 42:855–860.
   PubMed Web of Science ®Google Scholar
• Wise, G.E., Que, B.G., and Huang, H. (1999). Synthesis and secretion of MCP-1 by dental follicle cells—Implications for tooth eruption. J. Dent. Res. 78:1677–1681.
   PubMed Web of Science ®Google Scholar
• Liu, D., and Wise, G.E. (2008). Expression of endothelial monocyte-activating polypeptide II in the rat dental follicle and its potential role in tooth eruption. Eur. J. Oral Sci. 116:334–340.
   PubMed Web of Science ®Google Scholar
• Liu, D., Yao, S., Pan, F., and Wise, G.E. (2005). Chronology and regulation of gene expression of RANKL in the rat dental follicle. Eur. J. Oral Sci. 113:404–409.
   PubMed Web of Science ®Google Scholar
• Wise, G.E., Yao, S., Odgren, P.R., and Pan, F. (2005). CSF-1 regulation of osteoclastogenesis for tooth eruption. J. Dent. Res. 84:837–841.
   PubMed Web of Science ®Google Scholar
• Rattner, A., Hsieh, J., Smallwood, P.M., Gilber, D.J., Copeland, N.G., Jenkins, N.A., and Nathans, J. (1997). A family of secreted proteins contains homology to the cystein-rich ligand-binding domain of frizzled receptors. PNAS 94:2859–2863.
   PubMed Web of Science ®Google Scholar
• Li, C.H., and Amar, S. (2007). Inhibition of SFRP-1 reduces severity of periodontitis. J. Dent. Res. 86:873–877.
   PubMed Web of Science ®Google Scholar
• Hoang, B.H., Thomas, J.T., Abdul-Karim, F.W., Correia, K.M., Conlon, R.A., Luyten, F.P., and Ballock, R.T. (1998). Expression pattern of two frizzled-related genes, Frzb-1 and Sfrp-1, during mouse embryogenesis suggests a role for modulating action of Wnt family members. Dev. Dyn. 212:364–372.
   PubMed Web of Science ®Google Scholar
• Fukui, K., Kondo, M., Ito, G., Maeda, O., Sato, N., Yoshioka, H., Yokoi, K., Ueda, Y., Shimokata, K., and Seiko, Y. (2005). Transcriptional silencing of secreted related protein 1 (SFRP1) by promoter hypermethylation in non-small-cell lung cancer. Oncogene 24:6323–6327.
   PubMed Web of Science ®Google Scholar
• Han, X., and Amar, S. (2004). Secreted frizzled-related protein 1 (SFRP-1) protects fibroblasts from ceramide-induced apoptosis. J. Biol. Chem. 279:2832–2840.
   PubMed Web of Science ®Google Scholar
• Hausler, K.D., Horwood, N.J., Chuman, Y., Fisher, J., Ellis, J., Martin, T.J., Rubin, J.S., and Gillespie, M.T. (2004). Secreted frizzled-related protein-1 inhibits RANKL-dependent osteoclast formation. J. Bone Miner. Res. 19:1873–1881.
   PubMed Web of Science ®Google Scholar
• Bodien, P.V.N., Billiard, J., Moran, R.A., Ponce-de-Leon, H., McLarney, S., Mangine, A., Scrimo, M.J., Bhat, R.A., Stauffer, B., Green, J., Stein, G.S., Lian, J.B., and Komm, B.S. (2005). The Wnt antagonist secreted frizzled-related protein-1 controls osteoblast and osteocyte apoptosis. J. Cell Biochem. 96:1212–1230.
   PubMed Web of Science ®Google Scholar
• Bodine, P.V.N., Zhao, W., Kharode, Y.P., Bex, F.J., Lambert, A., Goad, M.E., Guar, T., Stein, G.S., Lian, J.B., and Komm, B.S. (2004). The Wnt antagonist secreted frizzled-related protein-1 is a negative regulator of trabecular bone formation in adult mice. Mol. Endocrinol. 18:1222–1237.
   PubMed Web of Science ®Google Scholar
• Yao, W., Cheng, Z., Shahnazar, M., Dai, W., Johnson, M.L., and Lane, N.E. (2010). Overexpression of secreted frizzled-related protein 1 inhibits bone formation and attenuates parathyroid hormone bone anabolic effects. J. Bone Miner. Res. 25:190–199.
   PubMed Web of Science ®Google Scholar
• Liu, D., and Wise, G.E. (2007). A DNA microarray analysis of chemokine and receptor genes in the rat dental follicle—Role of secreted frizzled-related protein-1 in osteoclastogenesis. Bone 41:266–272.
   PubMed Web of Science ®Google Scholar
• Cielinski, M.J., Jolie, M., Wise, G.E., Ando, D.G., and Marks, Jr., S.C. (1994). Colony-stimulating factor-1 (CSF-1) is a potent stimulator of tooth eruption in the rat. In The Biological Mechanisms of Tooth Eruption, Resorption and Replacement by Implants, Z. Davidovitch (ed.) pp. 429–436. Birmingham, AL: EBSCO Media.
   Google Scholar
• Wise, G.E., Lin, F., and Fan, W. (1992). Culture and characterization of dental follicle cells from rat molars. Cell Tissue Res. 267:483–492.
   PubMed Web of Science ®Google Scholar
• Wise, G.E., Ren, Y., and Yao, S. (2003). Regulation of osteoclastogenesis gene expression in dental follicle cells. J. Dent. Res. 82:298–302.
   PubMed Web of Science ®Google Scholar
• Wise, G.E., Lin, F., and Zhao, L. (1995). Immunolocalization of interleukin-1α in rat mandibular molars and its enhancement after in vivo injection of epidermal growth factor. Cell Tissue Res. 280:21–26.
   PubMed Web of Science ®Google Scholar
• Wise, G.E., and Yao, S. (2003). Expression of tumor necrosis factor-alpha in the rat dental follicle. Arch. Oral Biol. 48:47–54.
   PubMed Web of Science ®Google Scholar
• Boyle, W.J., Simonet, W.S., and Lacey, D.L. (2003). Osteoclast differentiation and activation. Nature 423:337–342.
   PubMed Web of Science ®Google Scholar
• Yasuda, H., Shima, N., Nakagawa, N., Mochizuki, S., Yano, K., Fujise, N., Sato, Y., Goto, M., Yamaguchi, K., Kuriyama, M., Kanno, T., Murakami, A., Tsuda, E., Morinaga, T., and Higasshio, K. (1998). Identity of osteoclastogenesis inhibitory factor (OCIF) and osteoprotegerin (OPG): A mechanism by which OPG/OCIF inhibits osteoclastogenesis in vitro. Endocrinology 139:1329–1337.
   PubMed Web of Science ®Google Scholar
• Wise, G.E., Lumpkin, S.J., Huang, H., and Zhang, Q. (2000). Osteoprotegerin and osteoclast differentiation factor in tooth eruption. J. Dent. Res. 79:1937–1942.
   PubMed Web of Science ®Google Scholar
• Van Wesenbeeck, L., Odgren, P.R., Mackay, C.A., D’Angelo, M., Safadi, F.F., Popoff, S.N., Hul, W.V., and Marks, S.C. (2002). The osteopetrotic mutation toothless (tl) is a loss-of-function frameshift mutation in the rat Csf1 gene: Evidence of a crucial role for CSF-1 in osteoclastogenesis and endochondral ossification. PNAS 99:14303–14308.
   PubMed Web of Science ®Google Scholar
• Wise, G.E., and Lin, F. (1994). Regulation and localization of colony-stimulating factor-1 mRNA in cultured rat dental follicle cells. Arch. Oral Biol. 39:621–627.
   PubMed Web of Science ®Google Scholar
• Hinterleitner, T.A., Saada, J.I., Berschneider, H.M., Powell, D.W., and Valentich, J.D. IL-1 stimulates intestinal myofibroblast COX gene expression and augments activation of CI-secretion in T84 cells. Am. J. Physio. Cell Physiol. 271:C1262–C1268.
   Google Scholar
• O’Connell, N.A., Kumar, A., Chatzipanteli, K., Mohan, A., Agarwal, R.K., Head, C., Bornstein, S.R., Abou-Samra, A.B., and Gwosdow, A.R. (1994). Interleukin-1 regulates corticosterone secretion from the rat adrenal gland through a catecholaminedependent and prostaglandin E2-independent mechanism. Endocrinology 135:460–467.
   PubMed Web of Science ®Google Scholar
• Azuma, Y., Kaji, K., Katogi, R., Takeshita, S., and Kudo, A. (2000). Tumor necrosis factor-alpha induces differentiation of and bone resorption by osteoclasts. J. Biol. Chem. 275:4858–4864.
   PubMed Web of Science ®Google Scholar