Beta-adrenergic receptors in hamster smooth muscle cells are transcriptionally regulated by glucocorticoids.

TLDR

Steroid hormones modulate adrenergic receptor responsiveness and receptor number. The study aimed to investigate how glucocorticoids regulate the beta‑2 adrenergic receptor gene. The authors examined the effects of triamcinolone acetonide on beta‑2 adrenergic receptor expression in DDT1MF‑2 hamster smooth muscle cells. Glucocorticoid treatment increased beta‑2 adrenergic receptor mRNA, receptor number, and adenylate cyclase activity, with transcription rates rising 3.1‑fold, demonstrating that glucocorticoids upregulate the receptor gene and enhance catecholamine responsiveness.

Abstract

Steroid hormones modulate adrenergic receptor responsiveness and receptor number. To investigate the regulation of the beta 2-adrenergic receptor gene by glucocorticoids we examined the effects of the synthetic glucocorticoid agonist triamcinolone acetonide on the expression of beta 2-adrenergic receptors in DDT1MF-2 hamster smooth muscle cells. Glucocorticoid treatment (1 X 10(-7) M) produced a 2.2 +/- 0.4-fold (n = 8) increase in beta 2-adrenergic receptor number (maximum) between 6 and 12 h) as determined by radioligand binding and a similar increase in catecholamine-stimulated adenylate cyclase activity. Steady-state levels of beta 2-adrenergic receptor mRNA, analyzed by Northern blot hybridization, were increased 2.4 +/- 0.4-fold (n = 6) within 1 h, while actin mRNA levels were unchanged throughout the experiment. These steroid-induced increases in beta 2-adrenergic receptor mRNA returned to control levels by 24 h and were followed by a much slower decline in beta 2-adrenergic receptor in plasma membranes. The rate of beta 2-adrenergic receptor gene transcription, assessed by nuclear run-off transcription assays, increased 3.1 +/- 0.1-fold (n = 2) in cells treated for 30 min with 1 X 10(-7) M triamcinolone acetonide. These studies indicate that glucocorticoids regulate the beta 2-adrenergic receptor-adenylate cyclase system by controlling the rate of transcription of the beta 2-adrenergic receptor gene and hence the responsiveness of the enzyme to catecholamine stimulation.