SEROTONIN PRODUCES BOTH HYPERPLASIA AND HYPERTROPHY OF BOVINE PULMONARY-ARTERY SMOOTH-MUSCLE CELLS IN CULTURE

Citation
Sl. Lee et al., SEROTONIN PRODUCES BOTH HYPERPLASIA AND HYPERTROPHY OF BOVINE PULMONARY-ARTERY SMOOTH-MUSCLE CELLS IN CULTURE, The American journal of physiology, 266(1), 1994, pp. 120000046-120000052
Citations number
30
Categorie Soggetti
Physiology
ISSN journal
00029513
Volume
266
Issue
1
Year of publication
1994
Part
1
Pages
120000046 - 120000052
Database
ISI
SICI code
0002-9513(1994)266:1<120000046:SPBHAH>2.0.ZU;2-6
Abstract
Serotonin [5-hydroxytryptamine (5-HT)] has a dual effect on bovine pul monary artery smooth muscle cells (SMC) in culture (S.-L. Lee, W. W. W ang, B. J. Moore, and B. L. Fanburg. Circ. Res. 68: 1382-1368, 1991.). Cellular internalization of 5-HT stimulates DNA synthesis and cellula r proliferation, whereas the action of 5-HT on a cell surface receptor elevates adenosine 3',5'-cyclic monophosphate and inhibits proliferat ion. The present study shows that 5-HT causes proliferation of both pu lmonary artery and aortic SMC but not of endothelial cells or fibrobla sts. Furthermore, c-myc and alpha- and beta-actin gene expressions of pulmonary artery SMC were elevated after 2-h incubation with 5-HT, bef ore stimulation of [H-3]thymidine incorporation. Actinomycin D (0.05 m u g/ml) but not cycloheximide (1 mu g/ml) inhibited the gene expressio n produced by 5-HT. Growth-arrested SMC progressed from a G(0) quiesce nt state through a normal cell cycle when subjected to 5-HT, 5-HT plus 25 ng/ml insulin-like growth factor, or 5-HT plus 0.5 ng/ml fibroblas t growth factor. Cell number increased by 20-40% at 40 h and 50-140% a t 7 days. Protein content of cells treated with 5-HT was elevated by 2 0-40% at 7 days, whereas the rate of protein synthesis, measured by [S -35]methionine incorporation, increased by 50-70% at 24 h. In the pres ence of 1 mu M 5-HT, cells enlarged by 70 and 100-200% at 40 h and 7 d ays, respectively. Thus internalization of 5-HT by SMC stimulates cell cycle-dependent gene expression, proliferative responses, and hypertr ophy of SMC in culture, and these actions may be important in vascular wall remodeling.