Title: Gender-Specific Modulation of the Response to Arterial Injury by Soluble Guanylate Cyclase alpha1
Authors: Vermeersch, Pieter ×
Buys, Emmanuel
Sips, Patrick
Pokreisz, Peter
Marsboom, Glenn
Gillijns, Hilde
Pellens, Marijke
Dewerchin, Mieke
Bloch, Kenneth D
Brouckaert, Peter
Janssens, Stefan #
Issue Date: 2009
Publisher: Bentham Open
Series Title: The Open Cardiovascular Medicine Journal vol:3 pages:98-104
Abstract: OBJECTIVE: Soluble guanylate cyclase (sGC), a heterodimer composed of alpha and beta subunits, synthesizes cGMP in response to nitric oxide (NO). NO modulates vascular tone and structure but the relative contributions of cGMP-dependent versus cGMP-independent mechanisms remain uncertain. We studied the response to vascular injury in male (M) and female (F) mice with targeted deletion of exon 6 of the sGCalpha1 subunit (sGCalpha1(-/-)), resulting in a non-functional heterodimer. METHODS: We measured aortic cGMP levels and mRNA transcripts encoding sGC alpha1, alpha2, and beta1 subunits in wild type (WT) and sGCa1(-/-) mice. To study the response to vascular injury, BrdU-incorporation and neointima formation (maximum intima to media (I/M) ratio) were determined 5 and 28 days after carotid artery ligation, respectively. RESULTS: Aortic cGMP levels were 4-fold higher in F than in M mice in both genotypes, and, within each gender, 4-fold higher in WT than in sGCa1(-/-). In contrast, sGCalpha1, sGCalpha2, and sGCbeta1 mRNA expression did not differ between groups. (3)H-thymidine incorporation in cultured sGCa1(-/-) smooth muscle cells (SMC) was 27%+/-12% lower than in WT SMC and BrdU-incorporation in carotid arteries 5 days after ligation was significantly less in sGCa1(-/-) M than in WT M. Neointima area and I/M 28 days after ligation were 65% and 62% lower in sGCa1(-/-) M than in WT M mice (p<0,05 for both) but were not different in F mice. CONCLUSION: Functional deletion of sGCa1 resulted in reduced cGMP levels in male sGCa1(-/-) mice and a gender-specific effect on the adaptive response to vascular injury.
ISSN: 1874-1924
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Molecular and Vascular Biology
Laboratory of Clinical Bacteriology and Mycology
Vesalius Research Centre (-)
Laboratory of Angiogenesis and Vascular Metabolism (Vesalius Research Center) (+)
× corresponding author
# (joint) last author

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