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PMID: 8119989 Published · ppublish English Journal Article

Immediate-early gene expression in response to hypertrophic and proliferative stimuli in pulmonary arterial smooth muscle cells.

The Journal of biological chemistry ·Vol. 269 ·No. 9 ·1994-03-04 ·Pages 6399-404

Rothman A, Wolner B, Button D, Taylor P

Abstract

Remodeling of the pulmonary vascular tree in pulmonary hypertension is associated with hypertrophy and proliferation of smooth muscle cells. Since the stimuli and signaling pathways for these processes are not well understood, we used a rat pulmonary arterial smooth muscle cell line (PAC1) to examine the effects of thrombin and platelet-derived growth factor (PDGF) on cellular growth and immediate-early gene expression. Over 72 h, thrombin (1 unit/ml) caused hypertrophy as reflected by a 102 +/- 12% increase in protein synthesis and a 49 +/- 11% increase in protein content per cell, but no change in cell number. PDGF (2.5 ng/ml) stimulated proliferation as evidenced by an increase in cell number (doubling in 5 days), but no significant change in protein content per cell. Immediate-early gene expression was examined by Northern blotting: both thrombin and PDGF induced egr-1, c-fos, c-jun, junB, and fra-1 mRNAs within 15 min; the response was maximal at 30-60 min (increases ranging from 2.9- to 9.3-fold over control serum-deprived cells) and returned to base-line levels within 2-4 h. Neither agent affected junD mRNA levels. However, thrombin but not PDGF, caused an increase in fosB mRNA levels (7.7 +/- 4.0-fold higher than control, n = 12, p < 0.0005). The immediate-early gene response to both agonists was generally dependent on extracellular Ca2+, Na2+/H+ exchange, and protein kinase C activation, but not on cAMP. The exception was c-jun mRNA, the levels of which were not affected by inhibition of protein kinase C, but decreased significantly by prevention of cAMP formation. Thapsigargin-sensitive intracellular Ca2+ stores were necessary for the response to thrombin, but not to PDGF. These results demonstrate that thrombin is a hypertrophic agent and that PDGF is a proliferative agent in PAC1 cells. These two agonists stimulate increases in a variety of immediate-early gene mRNAs, but only thrombin induces fosB mRNA.

Related Genes
MeSH Terms
Animals Calcium/metabolism Cell Division/drug effects Cell Line Egtazic Acid/pharmacology Gene Expression/drug effects Genes, Immediate-Early Genes, fos/drug effects Genes, jun/drug effects Hypertrophy Kinetics Muscle, Smooth, Vascular/cytology,drug effects,metabolism Platelet-Derived Growth Factor/pharmacology Protein Biosynthesis Protein Kinase C/metabolism Pulmonary Artery/cytology,drug effects,metabolism RNA, Messenger/biosynthesis Rats Sodium/pharmacology Sodium-Hydrogen Exchangers/metabolism Thrombin/pharmacology Transcription, Genetic/drug effects
Chemicals
Platelet-Derived Growth Factor RNA, Messenger Sodium-Hydrogen Exchangers Egtazic Acid Sodium Protein Kinase C Thrombin Calcium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Rothman A
Department of Pediatrics, University of California at San Diego, La Jolla 92093.
Wolner B
Button D
Taylor P
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1994-03-04
Pages
6399-404
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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