Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

CiteULike is a free service for managing and discovering scholarly references - click here to get started.

Sign In to gain access to subscriptions and/or personal tools.
Critical Reviews in Oral Biology & Medicine
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
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
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 HighWire
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Prime, S.S.
Right arrow Articles by Paterson, I.C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

TGF-β SIGNAL TRANSDUCTION IN ORO-FACIAL HEALTH AND NON-MALIGNANT DISEASE (PART I)

S.S. Prime*, M. Pring, M. Davies and I.C. Paterson

Department of Oral and Dental Science, Division of Oral Medicine, Pathology and Microbiology, Bristol Dental Hospital and School, University of Bristol, Lower Maudlin Street, Bristol BS1 2LY, UK;


Figure 1
View larger version (61K):
[in this window]
[in a new window]

 
Figure 1. TGF-β receptor activation. TGF-β initiates signaling by the assembly of receptor complexes involving two transmembrane serine-threonine kinase receptors (TβR-I and TβR-II). Following binding of TGF-β to TβR-II, TβR-I is recruited to form a heterotetrameric complex and is phosphorylated at serine residues within its GS domain by the constitutively active TβR-II. The activated TβR-I then activates a cascade of downstream signaling events that ultimately regulates gene transcription.

 

Figure 2
View larger version (30K):
[in this window]
[in a new window]

 
Figure 2. Structure of Smad proteins. The R and Co-Smads show considerable homology within both the MH1 and MH2 domains. The MH domains are separated by a variable proline-rich linker region, which, in the case of Smad4, contains a Smad activation domain (SAD). **Smad2 is unable to bind directly to DNA, due to a 30-amino-acid insertion within exon3 of the MH1 domain. I-Smads have C-terminal domains structurally similar to R and Co-Smads. The N-terminus, however, fails to show significant homology.

 

Figure 3
View larger version (49K):
[in this window]
[in a new window]

 
Figure 3. Smad signaling. The activated TβR-I kinase phosphorylates the R-Smads, Smad2 and Smad3, which then form heterodimers with the Co-Smad, Smad4. The complex translates to the nucleus and regulates gene transcription by binding directly to DNA via interactions with DNA-binding proteins and/or transcriptional co-activators and co-repressors. The transcription of the I-Smad, Smad7, is induced, and Smad7 exits the nucleus to control the intensity and duration of signaling via a negative feedback mechanism.

 

Figure 4
View larger version (43K):
[in this window]
[in a new window]

 
Figure 4. Cellular effects of TGF-β. TGF-β is a multi-functional cytokine that inhibits epithelial cell growth, induces apoptosis in a variety of cell types, stimulates new vessel growth, and is a potent immunosuppressant. In addition, TGF-β functions to elaborate the extracellular matrix.

 

Critical Reviews in Oral Biology & Medicine, Vol. 15, No. 6, 324-336 (2004)
DOI: 10.1177/154411130401500602


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