scholarly journals Transforming growth factor-β receptor and fibronectin expressions in aortic smooth muscle cells in diabetic rats

Diabetologia ◽  
1997 ◽  
Vol 40 (4) ◽  
pp. 383-391 ◽  
Author(s):  
T. Kanzaki ◽  
R. Shiina ◽  
Y. Saito ◽  
L. Zardi ◽  
N. Morisaki
2001 ◽  
Vol 20 (3) ◽  
pp. 171-181 ◽  
Author(s):  
Patricia Mestries ◽  
Catherine Alexakis ◽  
Dulce Papy-Garcia ◽  
Arlette Duchesnay ◽  
Denis Barritault ◽  
...  

1986 ◽  
Vol 102 (4) ◽  
pp. 1217-1223 ◽  
Author(s):  
R K Assoian ◽  
M B Sporn

A specific radioimmunoassay for type beta transforming growth factor (TGF-beta) was developed and used to show that human platelets treated with thrombin release TGF-beta as a consequence of degranulation. The thrombin concentrations required to induce release of TGF-beta parallel those concentrations that release the alpha-granule marker, beta-thromboglobulin. Related studies showed that TGF-beta acts on early passage, explant cultures of bovine aortic smooth muscle cells by inhibiting the effect of mitogens on proliferation of subconfluent cell monolayers yet synergizing with mitogens to stimulate growth of the same cells when cultured in soft agar. The results show that primary cultures of bovine aortic smooth muscle cells and established normal rat kidney cells behave similarly with regard to TGF-beta action. Moreover, the data suggest that platelet-mediated proliferation of aortic smooth muscle cells in vivo may not result solely from the stimulatory effect of platelet-derived growth factor (PDGF), but rather from an interaction of platelet factors which has the intrinsic ability to limit as well as stimulate mitosis.


Sign in / Sign up

Export Citation Format

Share Document