Key result
Pertussis toxin totally abolishes serotonin-induced DNA synthesis in aortic smooth muscle cells without affecting PDGF.
Why the study?
The signaling pathway by which serotonin induces DNA synthesis in vascular smooth muscle cells was not fully understood, particularly regarding pertussis toxin sensitivity.
Serotonin-induced DNA synthesis in vascular smooth muscle cells requires a novel pertussis toxin-sensitive pathway independent of cAMP, phosphoinositide hydrolysis, or calcium mobilization.
Should not change clinical practice; hypothesis-generating for pertussis toxin-sensitive G-protein pathways in vascular proliferation.
Serotonin-induced DNA synthesis in bovine aortic smooth muscle cells was totally abolished by pretreatment of cultures with 5 ng/ml pertussis toxin. The half maximally effective concentration of toxin was approximately 10 pg/ml. Pertussis toxin did not affect platelet-derived growth factor (PDGF)-stimulated DNA synthesis and actually enhanced the mitogenic effect of the phorbol ester, phorbol 12-myristate 13-acetate. Pertussis toxin did not inhibit serotonin-stimulated inositol phosphate accumulation or increases in intracellular calcium or cAMP concentrations under conditions sufficient to completely inhibit serotonin-induced (3H)thymidine incorporation. These results demonstrate that a novel, pertussis-sensitive pathway is required for serotonin-, but not platelet-derived growth factor-induced DNA synthesis in vascular smooth muscle cells. The pertussis-sensitive step does not involve cAMP, phosphoinositide hydrolysis, mobilization of intracellular calcium, or phorbol ester-sensitive protein kinase C activity.
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Kavanaugh et al. (1988) studied this question. Pertussis toxin was evaluated on Serotonin-induced DNA synthesis. Pretreatment with pertussis toxin totally abolished serotonin-induced DNA synthesis in bovine aortic smooth muscle cells without affecting PDGF-stimulated DNA synthesis.
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