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Medical Research Centre, Prince Henrys Hospital Melbourne, Victoria 3004, Australia
Address requests for reprints to: Dr. John W. Funder, Medical Research Centre, Prince Henrys Hospital, St. Kilda Road, Melbourne, Victoria 3004, Australia.
Abstract
To examine the direct effects of steroids on vascular smooth muscle, we have incubated rat aortic vascular smooth muscle cells in culture either steroid-free, or with natural and synthetic corticosteroids (RU26988, dexamethasone, corticosterone, 9
-fluorocortisol, aldosterone, deoxycorticosterone) or sex steroids (estradiol, 5
a-dihydrotestos,terone). At the end of 24 h, cultures were pulsed with [36S]ethionine for 2 h, the cells lysed, and patterns of incorporation of isotope into protein determined by two-dimensional gel electrophoresis and autoradiography. Neither estradiol nor 5
-dihydrotestosterone altered protein synthetic profiles compared with control (steroid-free) incubations. In contrast, cultures exposed to the six corticosteroids at 10–7 M showed an identical pattern of response (6 proteins increased, 6 proteins decreased). This response appears to be glucocorticoid specific, since the mineralocorticoids (9
fluorocortisol, aldosterone, and deoxycorticosterone) did not have any effects over and above those seen with the pure glucocorticoid RU26988. We interpret these data as evidence for a putative glucocorticoid domain of at least 12 proteins in rat vascular smooth muscle cells. In contrast, there appear to be no comparable estrogen-, androgen-, or mineralocorticoid-specific changes in these cells. (Endocrinology 113: 1096, 1983)
Footnotes
* This work was supported by the National Health and Medical Research Council of Australia and presented in part at the Joint Annual Meeting of The Endocrine Society of Australia and the New Zealand Society of Endocrinology, Christchurch, New Zealand, 1981.
Supported by a Jeane B. Kempner Fellowship from the University of Texas Medical Branch, Galveston, TX.
Received November 8, 1982.
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