REGULATION BY PROTEIN-KINASE-C OF TRANSFORMING GROWTH FACTOR-BETA(1) ACTION ON THE PROLIFERATION OF VASCULAR SMOOTH-MUSCLE CELLS FROM SPONTANEOUSLY HYPERTENSIVE RATS
J. Saltis et A. Bobik, REGULATION BY PROTEIN-KINASE-C OF TRANSFORMING GROWTH FACTOR-BETA(1) ACTION ON THE PROLIFERATION OF VASCULAR SMOOTH-MUSCLE CELLS FROM SPONTANEOUSLY HYPERTENSIVE RATS, Clinical and experimental pharmacology and physiology, 23(6-7), 1996, pp. 573-575
I, This study examined the role of protein kinase C (PKC) on the actio
n of transforming growth factor-beta(1) (TGF-beta(1)) to regulate the
proliferation of vascular smooth muscle cells (VSMC) isolated from the
aorta of the spontaneously hypertensive rat (SHR), 2. Down-regulation
of PKC by prolonged exposure to phorbol 12-myristate 13-acetate (PMA)
completely inhibited the ability of TGF-beta(1) to potentiate epiderm
al growth factor-stimulated proliferation of VSMC, 3. In contrast, the
inhibitory effect of TGF-beta 1 on serum-stimulated proliferation of
VSMC was not altered by PMA action. 4. These results suggest that PKC-
dependent signalling pathways involved in the regulation of growth by
TGF-beta(1) may be important in any proliferative component of vascula
r hypertrophy that develops in the SHR.