Regulator of G protein signaling 5 marks peripheral arterial smooth muscle cells and is downregulated in atherosclerotic plaque

被引:55
作者
Li, J
Adams, LD
Wang, X
Pabon, L
Schwartz, SM
Sane, DC
Geary, RL
机构
[1] Wake Forest Univ, Sch Med, Div Surg Sci, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Sch Med, Dept Surg, Winston Salem, NC 27157 USA
[3] Wake Forest Univ, Sch Med, Dept Cardiol, Winston Salem, NC 27157 USA
[4] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
关键词
D O I
10.1016/j.jvs.2004.06.021
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective: Regulator of G protein signaling 5 (RGS5), an inhibitor of Galpha(q) and Galpha(i) activation, was recently identified among genes highly expressed in smooth muscle cells (SMCs) of aorta but not vena cava. This finding prompted the 9 hypothesis that RGS5 provides long-term G protein inhibition specific to normal arterial SMC populations and that loss of expression may in turn contribute to arterial disease. Methods: To test this hypothesis we characterized RGS5 gene expression throughout the vasculature of nonhuman primates to determine whether RGS5 was restricted to arteries in other vascular beds and whether expression was altered in arterial disease. Results: In situ hybridization localized RGS5 message to medial SMCs of peripheral arteries, including carotid, iliac, mammary, and renal arteries, but not accompanying veins. SMCs of many small arteries and arterioles also expressed RGS5, including glomerular afferent arterioles critical to blood pressure regulation. Differential expression persisted in culture, inasmuch as RGS5 message was significantly higher in SMCs derived from arteries than from veins at real-time polymerase chain reaction. It was remarkable that the only major arterial bed lacking RGS5 was the coronary circulation. In atherosclerotic peripheral arteries RGS5 was expressed in medial SMCs, but was sharply downregulated in plaque SMCs. Conclusion: These data identify RGS5 as a new member of a short list of genes uniquely expressed in peripheral arteries but not coronary arteries. Persistence of an arterial pattern of RGS5 expression in culture and lack of expression in coronary arteries support a unique SMC phenotype fixed by distinct lineage or differentiation pathways. The association between loss of expression and arterial wall disease has prompted the new hypothesis that prolonged inhibition by RGS5 of vasoactive or trophic G protein signaling is critical to normal peripheral artery function.
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页码:519 / 528
页数:10
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