Sumiyoshi Katsuhiko, Mokuno Hiroshi, Iesaki Takafumi, Shimada Kazunori, Miyazaki Tetsuro, Kume Atsumi, Kiyanagi Takashi, Kuremoto Kenichi, Watanabe Yoshiro, Tada Nobuhiro, Daida Hiroyuki
Department of Cardiology, Juntendo University Graduate School of Medicine, 2-1-1, Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.
Cardiovasc Res. 2008 Dec 1;80(3):463-70. doi: 10.1093/cvr/cvn206. Epub 2008 Aug 11.
To clarify the role of Fc receptors (FcR) for immunoglobulin in endothelial dysfunction induced by hypercholesterolaemia, we evaluated the effect of deletion of the FcR gamma chain on endothelium-dependent relaxation and oxidative stress after 10 weeks on a high-fat diet in FcR gamma(-/-) mice compared with that in wild-type mice.
Plasma cholesterol levels of those on the high-fat diet were significantly increased compared with those on the normal chow diet in both groups of mice. Endothelium-dependent relaxation of the aortic ring with acetylcholine in wild-type mice was significantly reduced by the high-fat diet (ED(50): 0.22 vs. 0.43 nM, P < 0.002), whereas the relaxation in FcR gamma(-/-) mice was not inhibited (ED(50): 0.22 vs. 0.23 nM, NS). Furthermore, superoxide detection by dihydroethidium-derived fluorescence and immunohistochemical staining of p22phox expression were significantly increased in wild-type mice fed on the high-fat diet, while these oxidative stresses in FcR gamma(-/-) mice were not enhanced by the high-fat diet. Oil Red O-staining showed no significant lipid accumulation at the aortic sinus in both groups of mice.
This study demonstrates that the deletion of the FcR gamma chain preserves the endothelial function and attenuates oxidative stress affected by hypercholesterolaemia in FcR gamma(-/-) mice. These results indicate that FcR may play the pivotal role in endothelial dysfunction through oxidative stress induced by hypercholesterolaemia.
为阐明免疫球蛋白的Fc受体(FcR)在高胆固醇血症诱导的内皮功能障碍中的作用,我们评估了FcRγ链缺失对FcRγ(-/-)小鼠和野生型小鼠高脂饮食10周后内皮依赖性舒张和氧化应激的影响。
两组小鼠中,高脂饮食组的血浆胆固醇水平均显著高于正常饮食组。高脂饮食使野生型小鼠主动脉环对乙酰胆碱的内皮依赖性舒张显著降低(半数有效剂量:0.22对0.43 nM,P<0.002),而FcRγ(-/-)小鼠的舒张未受抑制(半数有效剂量:0.22对0.23 nM,无显著性差异)。此外,高脂饮食喂养的野生型小鼠中,二氢乙锭衍生荧光法检测超氧化物以及p22phox表达的免疫组化染色均显著增加,而高脂饮食并未增强FcRγ(-/-)小鼠的这些氧化应激。油红O染色显示两组小鼠主动脉窦均无明显脂质蓄积。
本研究表明,FcRγ链缺失可维持FcRγ(-/-)小鼠的内皮功能,并减轻高胆固醇血症所致的氧化应激。这些结果表明,FcR可能在高胆固醇血症诱导的氧化应激所致内皮功能障碍中起关键作用。