Wadsworth Center, New York State Department of Health, and School of Public Health, State University of New York, Albany, New York 12201-0509.
Wadsworth Center, New York State Department of Health, and School of Public Health, State University of New York, Albany, New York 12201-0509.
J Biol Chem. 2012 May 18;287(21):17777-17788. doi: 10.1074/jbc.M112.354274. Epub 2012 Mar 27.
NADPH-cytochrome P450 reductase (POR) is essential for the functioning of microsomal cytochrome P450 (P450) monooxygenases and heme oxygenases. The biological roles of the POR-dependent enzymes in the intestine have not been defined, despite the wealth of knowledge on the biochemical properties of the various oxygenases. In this study, cDNA microarray analysis revealed significant changes in gene expression in enterocytes isolated from the small intestine of intestinal epithelium-specific Por knock-out (named IE-Cpr-null) mice compared with that observed in wild-type (WT) littermates. Gene ontology analyses revealed significant changes in terms related to P450s, transporters, cholesterol biosynthesis, and, unexpectedly, antigen presentation/processing. The genomic changes were confirmed at either mRNA or protein level for selected genes, including those of the major histocompatibility complex class II (MHC II). Cholesterol biosynthetic activity was greatly reduced in the enterocytes of the IE-Cpr-null mice, as evidenced by the accumulation of the lanosterol metabolite, 24-dihydrolanosterol. However, no differences in either circulating or enterocyte cholesterol levels were observed between IE-Cpr-null and WT mice. Interestingly, the levels of the cholesterol precursor farnesyl pyrophosphate and its derivative geranylgeranyl pyrophosphate were also increased in the enterocytes of the IE-Cpr-null mice. Furthermore, the expression of STAT1 (signal transducer and activator of transcription 1), a downstream target of geranylgeranyl pyrophosphate signaling, was enhanced. STAT1 is an activator of CIITA, the class II transactivator for MHC II expression; CIITA expression was concomitantly increased in IE-Cpr-null mice. Overall, these findings provide a novel and mechanistic link between POR-dependent enzymes and the expression of MHC II genes in the small intestine.
NADPH-细胞色素 P450 还原酶 (POR) 对于微粒体细胞色素 P450 (P450) 单加氧酶和血红素加氧酶的功能至关重要。尽管对各种加氧酶的生化特性有丰富的了解,但 POR 依赖性酶在肠道中的生物学作用尚未确定。在这项研究中,与野生型 (WT) 同窝仔相比,从小肠上皮细胞特异性 Por 敲除 (命名为 IE-Cpr-null) 小鼠分离的肠细胞中的基因表达的 cDNA 微阵列分析显示出显著变化。基因本体论分析显示,与 P450、转运蛋白、胆固醇生物合成以及出乎意料的抗原呈递/加工相关的术语发生了显著变化。选择基因(包括主要组织相容性复合体 II (MHC II) 基因)的基因组变化在 mRNA 或蛋白质水平上得到了证实。胆固醇生物合成活性在 IE-Cpr-null 小鼠的肠细胞中大大降低,这表现为羊毛甾醇代谢物 24-二氢羊毛甾醇的积累。然而,IE-Cpr-null 和 WT 小鼠之间循环或肠细胞胆固醇水平没有差异。有趣的是,胆固醇前体法呢基焦磷酸及其衍生物香叶基焦磷酸的水平在 IE-Cpr-null 小鼠的肠细胞中也增加了。此外,STAT1(信号转导和转录激活因子 1)的表达增强,STAT1 是 geranylgeranyl pyrophosphate 信号的下游靶标。STAT1 是 MHC II 表达的 II 类转录激活物 CIITA 的激活剂;IE-Cpr-null 小鼠中 CIITA 表达同时增加。总体而言,这些发现为 POR 依赖性酶与小肠中 MHC II 基因的表达之间提供了一种新的机制联系。