Effects of apoE genotype on macrophage inflammation and heme oxygenase-1 expression

被引:87
作者
Jofro-Monseny, Laia [1 ]
Loboda, Agnieszka [2 ]
Wagner, Anika E. [1 ]
Huebbe, Patricia [1 ]
Boesch-Saadatmandi, Christine [1 ]
Jozkowicz, Alicja [2 ]
Minihane, Anne-Marie [3 ]
Dulak, Jozef [2 ]
Rimbach, Gerald [1 ]
机构
[1] Univ Kiel, Inst Human Nutr & Food Sci, Hermann Rodewald Str 6, D-24098 Kiel, Germany
[2] Jagiellonian Univ, Fac Biochem Biophys & Biotechnol, Dept Med Biotechnol, PL-30387 Krakow, Poland
[3] Univ Reading, Sch Chem Food Biosci & Pharm, Reading RG6 6AP, Berks, England
基金
英国惠康基金;
关键词
apoE genotype; macrophage; cytokines; nuclear factor kappa B; heme oxygenase-1; tumour necrosis factor alpha; inflammation; oxidative stress; redox signalling;
D O I
10.1016/j.bbrc.2007.03.150
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In order to gain a more comprehensive understanding of the aetiology of apolipoprotein E4 genotype-cardiovascular disease (CVD) associations, the impact of the apoE genotype on the macrophage inflammatory response was examined. The murine monocyte-macrophage cell line (RAW 264.7) stably transfected to produce equal amounts of human apoE3 or apoE4 was used. Following LPS stimulation, apoE4-macrophages showed higher and lower concentrations of tumour necrosis factor alpha (pro-inflammatory) and interleukin 10 (anti-inflammatory), respectively, both at mRNA and protein levels. In addition, increased expression of heme oxygenase-1 (a stress-induced anti-inflammatory protein) was observed in the apoE4-cells. Furthermore, in apoE4-macrophages, an enhanced transactivation of the key redox sensitive transcription factor NF-kappa B was shown. Current data indicate that apoE4 macrophages have an altered inflammatory response, which may contribute to the higher CVD risk observed in apoE4 carriers. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:319 / 324
页数:6
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