Hypoxia promotes human pulmonary artery smooth muscle cell proliferation through induction of arginase.

Abstract

Vascular remodeling and smooth muscle cell proliferation are hallmark pathogenic features of pulmonary artery hypertension (PAH). Alterations in the metabolism of l-arginine via arginase and nitric oxide synthase play a critical role in the endothelial dysfunction seen in PAH. l-arginine metabolism by arginase produces l-ornithine and urea. l-ornithine is a precursor for polyamine and proline synthesis, ultimately leading to an increase in cellular proliferation. Given the integral role of the smooth muscle layer in the pathogenesis of hypoxia-induced PAH, we hypothesized that hypoxia would increase cellular proliferation via arginase induction in human pulmonary artery smooth muscle cells (hPASMC). We found that arginase II mRNA and protein expression were significantly increased in cultured hPASMC exposed to 1% O(2) for 24 and 48 h, which coincided with an increase in arginase activity at 48 h. There were no hypoxia-induced changes in levels of arginase I mRNA or protein in cultured hPASMC. Exposure to hypoxia resulted in more than one and a half times as many viable cells after 120 h than normoxic exposure. The addition of the arginase inhibitor, S-(2-boronoethyl)-l-cysteine, completely prevented both the hypoxia-induced increase in arginase activity and proliferation in hPASMC. Furthermore, transfection of small interfering RNA (siRNA) targeting arginase II in hPASMC resulted in knockdown of arginase II protein levels and complete prevention of the hypoxia-induced cellular proliferation. These data support our hypothesis that hypoxia increases proliferation of hPASMC through the induction of arginase II.

• Authors: Bernadette Chen, Andrea E Calvert, Hongmei Cui, Leif D Nelin
• Journal: American journal of physiology. Lung cellular and molecular physiology (Am J Physiol Lung Cell Mol Physiol) Vol. 297 Issue 6 Pg. L1151-9 (Dec 2009) ISSN: 1522-1504 [Electronic] United States
• PMID: 19801451 (Publication Type: Journal Article)

Chemical References

• (2-boronoethyl)-cysteine
• Boronic Acids
• RNA, Messenger
• RNA, Small Interfering
• Arginase

Topics

• Arginase (antagonists & inhibitors, biosynthesis, genetics)
• Boronic Acids (pharmacology)
• Cell Proliferation (drug effects)
• Cells, Cultured
• Enzyme Induction (drug effects)
• Humans
• Hypoxia (enzymology, pathology)
• Myocytes, Smooth Muscle (drug effects, enzymology, pathology)
• Pulmonary Artery (cytology, drug effects, enzymology)
• RNA, Messenger (genetics, metabolism)
• RNA, Small Interfering (metabolism)