Graves Joan P, Gruzdev Artiom, Bradbury J Alyce, DeGraff Laura M, Li Huiling, House John S, Hoopes Samantha L, Edin Matthew L, Zeldin Darryl C
Immunity, Inflammation, and Disease Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina.
Immunity, Inflammation, and Disease Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina
Drug Metab Dispos. 2015 Aug;43(8):1169-80. doi: 10.1124/dmd.115.064139. Epub 2015 May 20.
Members of the cytochrome P450 CYP2J subfamily are expressed in multiple tissues in mice and humans. These enzymes are active in the metabolism of fatty acids to generate bioactive compounds. Herein we report new methods and results for quantitative polymerase chain reaction (qPCR) analysis for the seven genes (Cyp2j5, Cyp2j6, Cyp2j8, Cyp2j9, Cyp2j11, Cyp2j12, and Cyp2j13) of the mouse Cyp2j subfamily. SYBR Green primer sets were developed and compared with commercially available TaqMan primer/probe assays for specificity toward mouse Cyp2j cDNA, and analysis of tissue distribution and regulation of Cyp2j genes. Each TaqMan primer/probe set and SYBR Green primer set were shown to be specific for their intended mouse Cyp2j cDNA. Tissue distribution of the mouse Cyp2j isoforms confirmed similar patterns of expression between the two qPCR methods. Cyp2j5 and Cyp2j13 were highly expressed in male kidneys, and Cyp2j11 was highly expressed in both male and female kidneys. Cyp2j6 was expressed in multiple tissues, with the highest expression in the small intestine and duodenum. Cyp2j8 was detected in various tissues, with highest expression found in the skin. Cyp2j9 was highly expressed in the brain, liver, and lung. Cyp2j12 was predominately expressed in the brain. We also determined the Cyp2j isoform expression in Cyp2j5 knockout mice to determine whether there was compensatory regulation of other Cyp2j isoforms, and we assessed Cyp2j isoform regulation during various inflammatory models, including influenza A, bacterial lipopolysaccharide, house dust mite allergen, and corn pollen. Both qPCR methods detected similar suppression of Cyp2j6 and Cyp2j9 during inflammation in the lung.
细胞色素P450 CYP2J亚家族的成员在小鼠和人类的多种组织中表达。这些酶在脂肪酸代谢以生成生物活性化合物的过程中具有活性。在此,我们报告了用于小鼠Cyp2j亚家族七个基因(Cyp2j5、Cyp2j6、Cyp2j8、Cyp2j9、Cyp2j11、Cyp2j12和Cyp2j13)定量聚合酶链反应(qPCR)分析的新方法和结果。开发了SYBR Green引物组,并与市售的TaqMan引物/探针检测法在对小鼠Cyp2j cDNA的特异性、Cyp2j基因的组织分布分析和调控方面进行了比较。每个TaqMan引物/探针组和SYBR Green引物组都显示对其预期的小鼠Cyp2j cDNA具有特异性。小鼠Cyp2j同工型的组织分布证实了两种qPCR方法之间相似的表达模式。Cyp2j5和Cyp2j13在雄性肾脏中高表达,Cyp2j11在雄性和雌性肾脏中均高表达。Cyp2j6在多种组织中表达,在小肠和十二指肠中表达最高。Cyp2j8在各种组织中均有检测到,在皮肤中表达最高。Cyp2j9在脑、肝和肺中高表达。Cyp2j12主要在脑中表达。我们还测定了Cyp2j5基因敲除小鼠中Cyp2j同工型的表达,以确定是否存在其他Cyp2j同工型的代偿性调控,并且我们评估了在包括甲型流感、细菌脂多糖、屋尘螨过敏原和玉米花粉在内的各种炎症模型中Cyp2j同工型的调控。两种qPCR方法均检测到肺炎症期间Cyp2j6和Cyp2j9受到类似抑制。