Effect of stretch on growth and collagen synthesis in cultured rat and lamb pulmonary arterial smooth muscle cells
- 1 December 1993
- journal article
- research article
- Published by Wiley in Journal of Cellular Physiology
- Vol. 157 (3) , 615-624
- https://doi.org/10.1002/jcp.1041570322
Abstract
There are no studies of the effect of stretch in cultured pulmonary vascular smooth muscle, and some data suggest that a stretch‐mediated increase in connective tissue synthesis in pulmonary arteries is mediated by the endothelium. To investigate whether stretch can serve as a growth stimulus in this smooth muscle, we studied two types of cultured pulmonary arterial smooth muscle cells (a multiply passaged clonal line of rat cells [PAC1], and early passage lamb cells [EPTC]). Cells were grown on a collagen‐coated silicone surface and subjected to repetitive stretch (0.33–0.5 Hz; 10–20% strain). The relative rates of total RNA, DNA, protein, and soluble collagen synthesis were determined using 3H precursors, and c‐fos and collagen mRNAs by Northern blot analysis. Stretch caused no significant change in the rate of RNA synthesis in either PAC1 cells (+9%) or EPTC (—3%). The relative rate of total protein synthesis was decreased by stretch (6% in PAC1 cells and 36% in EPTC [both NS]) as was the rate of collagen synthesis (−24% in EPTC [NS]). In EPTC, the percentage of 3H‐thymidine labeled cells was modestly increased with 24 h stretch (17 ± 5.7%; P ≤.001), but trichloroacetic acid (TCA) precipitated 3H‐thymidine was unaltered by stretch, and the number of cells not significantly changed with stretch. c‐fos mRNA expression was only inconsistently induced by stretch x30 min in EPTC, and not at all in PAC1 cells. Expression of mRNA for α1 (I) and α1 (III) collagen was not changed significantly by 24 h or 48 h of stretch. We conclude that stretch does not serve as a significant growth stimulus in cultured pulmonary vascular smooth muscle cells in this system. These findings do not rule out the possibility that stretch is a growth stimulus for these cells under different conditions, but do suggest that other models will be needed to determine if and how mechanical stimuli affect growth of pulmonary vascular smooth muscle.Keywords
This publication has 38 references indexed in Scilit:
- Stretch increases inositol trisphosphate and inositol tetrakisphosphate in cultured pulmonary vascular smooth muscle cellsBiochemical and Biophysical Research Communications, 1991
- Myosin heavy chain isoform diversity in smooth muscle is produced by differential RNA processingJournal of Molecular Biology, 1989
- Effect of normolipemic and hyperlipemic serum on biosynthetic response to cyclic stretching of aortic smooth muscle cells.Arteriosclerosis: An Official Journal of the American Heart Association, Inc., 1989
- Periodic organization of the contractile apparatus in smooth muscle revealed by the motion of dense bodies in single cells.The Journal of cell biology, 1989
- Heparin inhibits proliferation of fetal vascular smooth muscle cells in the absence of platelet‐derived growth factorJournal of Cellular Physiology, 1986
- Cloning of Type III Collagen and Expression in Aortic Smooth Muscle CellsAnnals of the New York Academy of Sciences, 1985
- Functional angiotensin II receptors in cultured vascular smooth muscle cells.The Journal of cell biology, 1982
- Pulmonary vascular disease with congenital heart lesions: pathologic features and causes.Circulation, 1981
- Proline and thymidine uptake in rabbit ear artery segments in vitro increased by chronic tangential load.Hypertension, 1980
- Use of a mixture of proteinase-free collagenases for the specific assay of radioactive collagen in the presence of other proteinsBiochemistry, 1971