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Journal of Dental Research, Vol. 82, No. 4,
298-302 (2003)
DOI: 10.1177/154405910308200411
Regulation of Osteoprotegerin Gene Expression in Dental Follicle Cells
G.E. Wise*,
Y. Ren and
S. Yao
Department of Comparative Biomedical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803;

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Figure 1. (A) Ethidium-bromide-stained gels of RT-PCR products for OPG, PTHrP-R, and CSF-1 after incubation of DFC with different concentrations of PMA. Note that PMA up-regulates OPG gene expression but down-regulates PTHrP-R and CSF-1 expression. In these and all subsequent graphs, the bars labeled with the same letters are not significantly different according to a LSD t test (P 0.05). (B) RT-PCR products for OPG, PTHrP-R, and CSF-1 after incubation of DFC with 50 ng/mL PMA over different time periods. Again, PMA enhances OPG expression (six-hour maximal effect) and decreases PTHrP-R and CSF-1 (six-hour maximum effect).
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Figure 2. (A) RT-PCR products for OPG, PTHrP, and CSF-1 after incubation of DFC with different concentrations of dbcAMP. Note that dbcAMP down-regulates OPG gene expression but conversely up-regulates PTHrP-R and CSF-1. (B) RT-PCR products for OPG, PTHrP-R, and CSF-1 after incubation of DFC with 5 µg/mL of dbcAMP over different time periods. Again, dbcAMP reduces OPG expression (six-hour maximum effect) and increases PTHrP-R (24-hour maximum) and CSF-1 (12-hour maximum) expression.
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Figure 4. Immunostaining of DFC for OPG in the absence of PMA (panel A) and after incubation with PMA at a concentration of 100 ng/mL for 12 hrs (panel B). Note the enhanced brown immunostain in the cells incubated with PMA in panel B.
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