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ATF-2 cooperates with Smad3 to mediate TGF-β effects on chondrocyte maturation
- Source :
-
Experimental Cell Research . Aug2003, Vol. 288 Issue 1, p198. 10p. - Publication Year :
- 2003
-
Abstract
- This study demonstrates that ATF-2 cooperates with Smad3 to regulate the rate of chondrocyte maturation in response to TGF-β. ATF-2 was rapidly phosphorylated in chick embryonic cephalic sternal chondrocytes following treatment with TGF-β, and the effect was dependent upon p38 kinase activity. Transient transfection of both wild-type ATF-2 or Smad3 activated the TGF-β-responsive reporter, p3TP-Lux, and synergistic effects were observed with ATF-2 and Smad3 coexpression. The effect of Smad3 and ATF-2 alone and in combination on chondrocyte maturation was examined in cultures simultaneously infected with RCAS viruses expressing different viral envelope proteins. When expressed alone, wild-type ATF-2 or Smad3 both inhibit colX expression and partially mimic the effects of exogenous TGF-β. However, in combination the effects were additive and similar to the inhibitory effects of TGF-β on colX expression. Loss of function experiments using dominant negative ATF-2 or Smad3 partially blocked the inhibitory effect of TGF-β on colX, while together the blockade was complete. Similar effects were observed with another TGF-β-responsive gene, PTHrP. However, the induction of colX by BMP-2 was not affected by overexpression of either wild-type or dominant negative ATF-2, indicating specificity for TGF-β signaling. In contrast, although TGF-β does not activate CRE/CREB signaling, dominant negative CREB enhanced colX expression in control and in TGF-β and BMP-2-treated cultures. Thus, ATF-2 regulates chondrocyte maturation as a direct target of TGF-β signaling while CREB regulates differentiation by targeting genes independent of the individual signaling effects of TGF-β or BMP-2. [Copyright &y& Elsevier]
- Subjects :
- *CARTILAGE cells
*ENZYMES
*VIRUS diseases
Subjects
Details
- Language :
- English
- ISSN :
- 00144827
- Volume :
- 288
- Issue :
- 1
- Database :
- Academic Search Index
- Journal :
- Experimental Cell Research
- Publication Type :
- Academic Journal
- Accession number :
- 10318474
- Full Text :
- https://doi.org/10.1016/S0014-4827(03)00181-2