Abstract:
:Treatment of human vascular smooth muscle cells (SMC) with human alpha-thrombin greatly increased DNA synthesis and cell proliferation. Both the integrity of the catalytic site and that of the anion binding exosite were required for expression of this activity. Experiments employing Northerns indicated induction of c-fos expression as well as a time-dependent induction of platelet-derived growth factor-A (PDGF-A) gene by thrombin. The thrombin mitogenic activity was potentiated by PDGF-BB, insulin and the vasoconstrictor peptide endothelin-1 suggesting synergism by convergence of intracellular growth-promoting signals. SMC treatment with pertussis toxin and forskolin indicated that the mitogenic activity of thrombin may be induced via signal transduction mechanism(s) involving changes in cAMP levels and activation of a Gi-like protein. These results suggest that thrombin may play a functional role in the regulation of human vascular SMC proliferation.
journal_name
FEBS Lettjournal_title
FEBS lettersauthors
Kanthou C,Parry G,Wijelath E,Kakkar VV,Demoliou-Mason Cdoi
10.1016/0014-5793(92)80961-fkeywords:
subject
Has Abstractpub_date
1992-12-14 00:00:00pages
143-8issue
2eissn
0014-5793issn
1873-3468pii
0014-5793(92)80961-Fjournal_volume
314pub_type
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