Abstract | BACKGROUND: METHODS AND RESULTS: We studied BMP/ TGF-beta signaling in 2 rat models of PAH due to chronic hypoxia and monocrotaline. In both models, there was a significant reduction in lung BMP type IA receptor and BMP type II receptor mRNA expression, although these changes were more pronounced in the monocrotaline model. This was accompanied by a reduction in lung levels of phospho-Smad1/5 and Id (inhibitor of DNA binding) gene expression in the monocrotaline model. In contrast, we observed increased TGF-beta activity, again more marked in the monocrotaline model, as evidenced by increased phospho-Smad2/3 and increased expression of TGF-beta-regulated genes. Immunohistochemistry revealed increased TGF-beta(1) expression in pulmonary artery smooth muscle cells and macrophages surrounding remodeled pulmonary arteries in monocrotaline rats. Inhibition of activin receptor-like kinase-5 signaling in vivo with the selective small-molecule inhibitor IN-1233 prevented PAH, right ventricular hypertrophy, and vascular remodeling after monocrotaline injection and inhibited the progression of established PAH in this model. No significant effect was observed in hypoxic PAH. In vitro studies confirmed that TGF-beta stimulated migration of distal rat pulmonary artery smooth muscle cells and that this effect was inhibited by IN-1233. CONCLUSIONS: Disruption of BMP/ TGF-beta signaling is more pronounced in the monocrotaline model of PAH than in the chronic hypoxia model. Increased TGF-beta activity is associated with greater macrophage recruitment with monocrotaline treatment. Inhibition of TGF-beta signaling via activin receptor-like kinase-5 prevents development and progression of PAH in the monocrotaline model and may involve inhibition of pulmonary artery smooth muscle cell migration.
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Authors | Lu Long, Alexi Crosby, Xudong Yang, Mark Southwood, Paul D Upton, Dae-Kee Kim, Nicholas W Morrell |
Journal | Circulation
(Circulation)
Vol. 119
Issue 4
Pg. 566-76
(Feb 03 2009)
ISSN: 1524-4539 [Electronic] United States |
PMID | 19153267
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- 3-((4-(6-methylpyridin-2-yl)-5-(quinolin-6-yl)-1H-imidazol-2-yl)methyl)benzamide
- Benzamides
- Bone Morphogenetic Proteins
- Quinolines
- RNA, Messenger
- Receptors, Transforming Growth Factor beta
- Transforming Growth Factor beta
- Monocrotaline
- Protein Serine-Threonine Kinases
- Bone Morphogenetic Protein Receptors, Type II
- Receptor, Transforming Growth Factor-beta Type I
- Tgfbr1 protein, rat
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Topics |
- Animals
- Benzamides
(pharmacology)
- Bone Morphogenetic Protein Receptors, Type II
(genetics, metabolism)
- Bone Morphogenetic Proteins
(metabolism)
- Cell Movement
(drug effects, physiology)
- Chronic Disease
- Disease Models, Animal
- Disease Progression
- Hypertension, Pulmonary
(chemically induced, drug therapy, metabolism)
- Hypoxia
(metabolism, pathology)
- Male
- Monocrotaline
- Muscle, Smooth, Vascular
(enzymology, pathology)
- Protein Serine-Threonine Kinases
(antagonists & inhibitors, metabolism)
- Quinolines
(pharmacology)
- RNA, Messenger
(metabolism)
- Rats
- Rats, Sprague-Dawley
- Receptor, Transforming Growth Factor-beta Type I
- Receptors, Transforming Growth Factor beta
(antagonists & inhibitors, metabolism)
- Signal Transduction
(physiology)
- Transforming Growth Factor beta
(metabolism)
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