Journal of Dental Research

 

Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Click here to sign up for SAGE Journal Email Alerts today!

Sign In to gain access to subscriptions and/or personal tools.
This Article
Right arrow Abstract Freely available
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Wise, G.E.
Right arrow Articles by Yao, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
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;


Figure 1
View larger version (46K):
[in this window]
[in a new window]

 
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).

 

Figure 2
View larger version (50K):
[in this window]
[in a new window]

 
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.

 

Figure 3
View larger version (29K):
[in this window]
[in a new window]

 
Figure 3. (A) RT-PCR products for PKC-{alpha} after incubation of DFC with PMA in either a concentration-dependent or time-dependent study. Note that PMA up-regulates PKC-{alpha} expression. (B) RT-PCR products for PKC-{alpha} after incubation of DFC with PTHrP in either a concentration-dependent or time-dependent study. PTHrP down-regulates PKC-{alpha} expression. (C) RT-PCR products for PKC-{alpha} after incubation of DFC with CSF-1 in either a concentration-dependent or time-dependent study. CSF-1 down-regulates PKC-{alpha} expression.

 

Figure 4
View larger version (36K):
[in this window]
[in a new window]

 
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.

 

Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?