Synergistic stimulation of parathyroid hormone-related peptide gene expression by mechanical stretch and angiotensin II in rat aortic smooth muscle cells

• Published in: The Journal of biological chemistry 1994-07, Vol.269 (27), p.17911-17917
• Main Authors: NODA, M, KATOH, T, TAKUWA, N, KUMADA, M, KUROKAWA, K, TAKUWA, Y
• Format: Article
• Language: English
• Subjects: Alkaloids - pharmacology; Aminoacids, peptides. Hormones. Neuropeptides; Analytical, structural and metabolic biochemistry; Angiotensin II - pharmacology; Animals; Aorta; Biological and medical sciences; Biomechanical Phenomena; Calcium - metabolism; Calcium Channel Blockers - pharmacology; Cells, Cultured; Cyclic AMP - metabolism; Down-Regulation; Enzyme Activation; Fundamental and applied biological sciences. Psychology; Molecular and cellular biology; Molecular genetics; Muscle, Smooth, Vascular - cytology; Muscle, Smooth, Vascular - metabolism; Nitrendipine - pharmacology; Parathyroid Hormone - genetics; Parathyroid Hormone-Related Protein; Protein Kinase C - antagonists & inhibitors; Protein-Tyrosine Kinases - antagonists & inhibitors; Proteins; Proteins - genetics; Rats; RNA, Messenger - metabolism; Staurosporine; Transcription. Transcription factor. Splicing. Rna processing
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(17)32396-7

Repetitive cyclic stretch (60 cycles/min) of rat aortic smooth muscle cells dramatically enhances the effect of angiotensin II (AII) on mRNA expression of the vasorelaxant, parathyroid hormone-related peptide (PTHrP). Thus, combined stimulation of rat aortic smooth muscle cells by cyclic stretch and low concentrations of AII, but not either alone, induces a synergistic, marked increase in the PTHrP mRNA level, in a manner dependent on the strength of stretch. This response is accompanied by a synergistic increase in secretion of PTHrP from smooth muscle cells. Removal of extracellular Ca2+ or addition of Ca2+ channel blockers, including Gd3+ and nitrendipine, does not considerably reduce the combined effects of stretch and AII, indicating that this response is not dependent on stretch-induced Ca2+ influx across the plasma membrane. The combined effect of stretch and AII on PTHrP mRNA expression is strongly attenuated by the protein kinase C (PKC) inhibitor staurosporine or by down-regulation of PKC, suggesting that PKC plays an important role in the synergistic response. However, stretch neither elicits activation of phospholipase C or PKC by itself, nor does it enhance AII-induced activation of these enzymes. These results indicate that in vascular smooth muscle cells mechanical stretch acts together with the vasoconstrictor AII to regulate the expression of the vasodilator PTHrP and suggest the role of PTHrP as a local modulator of myogenic tone.