Oxidative species increase arginase activity in endothelial cells through the RhoA/Rho kinase pathway

S. Chandra, M. J. Romero, A. Shatanawi, A. M. Alkilany, R. B. Caldwell, R. William Caldwell

Research output: Contribution to journalArticle

93 Citations (Scopus)

Abstract

Background and Purpose NO produced by endothelial NOS is needed for normal vascular function. During diabetes, aging and hypertension, elevated levels of arginase can compete with NOS for available l-arginine, reducing NO and increasing superoxide (O 2 .-) production via NOS uncoupling. Elevated O 2 .- combines with NO to form peroxynitrite (ONOO -), further reducing NO. Oxidative species increase arginase activity, but the mechanism(s) involved are not known. Our study determined the mechanism involved in peroxynitrite and hydrogen peroxide-induced enhancement in endothelial arginase activity. We hypothesized that oxidative species increase arginase activity through PKC-activated RhoA/Rho kinase (ROCK) pathway. Experimental approach Arginase activity/expression was analysed in bovine aortic endothelial cells (BAEC) treated with an ONOO - generator (SIN-1) or H 2O 2. Pretreatment with inhibitors of Rho kinase (Y-27632) or PKC (Gö6976) was used to investigate the mechanism involved in arginase activation. Key Results Exposure to SIN-1 (25 μM, 24 h) or H 2O 2 (25 μM, 8 h) increased arginase I expression and arginase activity (35% and 50%, respectively), which was prevented by ROCK inhibitor, Y-27632, PKC inhibitor, Gö6976 or siRNA to p115-Rho GEF. There was an early activation of p115-Rho GEF (SIN-1, 2 h; H 2O 2, 1 h) and Rho A (SIN-1, 4 h; H 2O 2, 1 h) that was prevented by using the PKC inhibitor. Exposure to SIN-1 and H 2O 2also reduced NOS activity, which was blocked by pretreatment with p115-RhoGEF siRNA. Conclusions and Implications Our data indicate that the oxidative species ONOO - and H 2O 2 increase arginase activity/expression through PKC-mediated activation of RhoA/Rho kinase pathway.

Original languageEnglish (US)
Pages (from-to)506-519
Number of pages14
JournalBritish Journal of Pharmacology
Volume165
Issue number2
DOIs
StatePublished - Jan 1 2012

Fingerprint

Arginase
rho-Associated Kinases
Endothelial Cells
Peroxynitrous Acid
Small Interfering RNA
Rho Guanine Nucleotide Exchange Factors
Superoxides
Hydrogen Peroxide
Blood Vessels
Arginine
Hypertension

Keywords

  • RhoA
  • arginase
  • hydrogen peroxide
  • peroxynitrite
  • protein kinase C

ASJC Scopus subject areas

  • Pharmacology

Cite this

Oxidative species increase arginase activity in endothelial cells through the RhoA/Rho kinase pathway. / Chandra, S.; Romero, M. J.; Shatanawi, A.; Alkilany, A. M.; Caldwell, R. B.; Caldwell, R. William.

In: British Journal of Pharmacology, Vol. 165, No. 2, 01.01.2012, p. 506-519.

Research output: Contribution to journalArticle

Chandra, S. ; Romero, M. J. ; Shatanawi, A. ; Alkilany, A. M. ; Caldwell, R. B. ; Caldwell, R. William. / Oxidative species increase arginase activity in endothelial cells through the RhoA/Rho kinase pathway. In: British Journal of Pharmacology. 2012 ; Vol. 165, No. 2. pp. 506-519.
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abstract = "Background and Purpose NO produced by endothelial NOS is needed for normal vascular function. During diabetes, aging and hypertension, elevated levels of arginase can compete with NOS for available l-arginine, reducing NO and increasing superoxide (O 2 .-) production via NOS uncoupling. Elevated O 2 .- combines with NO to form peroxynitrite (ONOO -), further reducing NO. Oxidative species increase arginase activity, but the mechanism(s) involved are not known. Our study determined the mechanism involved in peroxynitrite and hydrogen peroxide-induced enhancement in endothelial arginase activity. We hypothesized that oxidative species increase arginase activity through PKC-activated RhoA/Rho kinase (ROCK) pathway. Experimental approach Arginase activity/expression was analysed in bovine aortic endothelial cells (BAEC) treated with an ONOO - generator (SIN-1) or H 2O 2. Pretreatment with inhibitors of Rho kinase (Y-27632) or PKC (G{\"o}6976) was used to investigate the mechanism involved in arginase activation. Key Results Exposure to SIN-1 (25 μM, 24 h) or H 2O 2 (25 μM, 8 h) increased arginase I expression and arginase activity (35{\%} and 50{\%}, respectively), which was prevented by ROCK inhibitor, Y-27632, PKC inhibitor, G{\"o}6976 or siRNA to p115-Rho GEF. There was an early activation of p115-Rho GEF (SIN-1, 2 h; H 2O 2, 1 h) and Rho A (SIN-1, 4 h; H 2O 2, 1 h) that was prevented by using the PKC inhibitor. Exposure to SIN-1 and H 2O 2also reduced NOS activity, which was blocked by pretreatment with p115-RhoGEF siRNA. Conclusions and Implications Our data indicate that the oxidative species ONOO - and H 2O 2 increase arginase activity/expression through PKC-mediated activation of RhoA/Rho kinase pathway.",
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AU - Chandra, S.

AU - Romero, M. J.

AU - Shatanawi, A.

AU - Alkilany, A. M.

AU - Caldwell, R. B.

AU - Caldwell, R. William

PY - 2012/1/1

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N2 - Background and Purpose NO produced by endothelial NOS is needed for normal vascular function. During diabetes, aging and hypertension, elevated levels of arginase can compete with NOS for available l-arginine, reducing NO and increasing superoxide (O 2 .-) production via NOS uncoupling. Elevated O 2 .- combines with NO to form peroxynitrite (ONOO -), further reducing NO. Oxidative species increase arginase activity, but the mechanism(s) involved are not known. Our study determined the mechanism involved in peroxynitrite and hydrogen peroxide-induced enhancement in endothelial arginase activity. We hypothesized that oxidative species increase arginase activity through PKC-activated RhoA/Rho kinase (ROCK) pathway. Experimental approach Arginase activity/expression was analysed in bovine aortic endothelial cells (BAEC) treated with an ONOO - generator (SIN-1) or H 2O 2. Pretreatment with inhibitors of Rho kinase (Y-27632) or PKC (Gö6976) was used to investigate the mechanism involved in arginase activation. Key Results Exposure to SIN-1 (25 μM, 24 h) or H 2O 2 (25 μM, 8 h) increased arginase I expression and arginase activity (35% and 50%, respectively), which was prevented by ROCK inhibitor, Y-27632, PKC inhibitor, Gö6976 or siRNA to p115-Rho GEF. There was an early activation of p115-Rho GEF (SIN-1, 2 h; H 2O 2, 1 h) and Rho A (SIN-1, 4 h; H 2O 2, 1 h) that was prevented by using the PKC inhibitor. Exposure to SIN-1 and H 2O 2also reduced NOS activity, which was blocked by pretreatment with p115-RhoGEF siRNA. Conclusions and Implications Our data indicate that the oxidative species ONOO - and H 2O 2 increase arginase activity/expression through PKC-mediated activation of RhoA/Rho kinase pathway.

AB - Background and Purpose NO produced by endothelial NOS is needed for normal vascular function. During diabetes, aging and hypertension, elevated levels of arginase can compete with NOS for available l-arginine, reducing NO and increasing superoxide (O 2 .-) production via NOS uncoupling. Elevated O 2 .- combines with NO to form peroxynitrite (ONOO -), further reducing NO. Oxidative species increase arginase activity, but the mechanism(s) involved are not known. Our study determined the mechanism involved in peroxynitrite and hydrogen peroxide-induced enhancement in endothelial arginase activity. We hypothesized that oxidative species increase arginase activity through PKC-activated RhoA/Rho kinase (ROCK) pathway. Experimental approach Arginase activity/expression was analysed in bovine aortic endothelial cells (BAEC) treated with an ONOO - generator (SIN-1) or H 2O 2. Pretreatment with inhibitors of Rho kinase (Y-27632) or PKC (Gö6976) was used to investigate the mechanism involved in arginase activation. Key Results Exposure to SIN-1 (25 μM, 24 h) or H 2O 2 (25 μM, 8 h) increased arginase I expression and arginase activity (35% and 50%, respectively), which was prevented by ROCK inhibitor, Y-27632, PKC inhibitor, Gö6976 or siRNA to p115-Rho GEF. There was an early activation of p115-Rho GEF (SIN-1, 2 h; H 2O 2, 1 h) and Rho A (SIN-1, 4 h; H 2O 2, 1 h) that was prevented by using the PKC inhibitor. Exposure to SIN-1 and H 2O 2also reduced NOS activity, which was blocked by pretreatment with p115-RhoGEF siRNA. Conclusions and Implications Our data indicate that the oxidative species ONOO - and H 2O 2 increase arginase activity/expression through PKC-mediated activation of RhoA/Rho kinase pathway.

KW - RhoA

KW - arginase

KW - hydrogen peroxide

KW - peroxynitrite

KW - protein kinase C

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