首页> 美国卫生研究院文献>Cancer Science >Proline Is Required for Transcriptional Control of the Aromatic Hydrocarbon‐inducible P1450 Gene in C57BL/6 Mouse Monolayer‐cultured Hepatocytes
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Proline Is Required for Transcriptional Control of the Aromatic Hydrocarbon‐inducible P1450 Gene in C57BL/6 Mouse Monolayer‐cultured Hepatocytes

机译:脯氨酸是转录控制C57BL / 6小鼠单层培养的肝细胞中可诱导芳香烃诱导的P1450基因所必需的。

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摘要

Expression of aryl hydrocarbon hydroxylase (AHH) and the corresponding gene, CyplA1 or P1450 in mice, in C57BL/6 mouse hepatocytes in primary culture was investigated after exposure to benz[a]‐anthracene with respect to proline‐related metabolic regulation. When the cells were cultivated in complete Waymouth MB752/1 (Way), prominent induction of AHH by benz[a]anthracene was observed, whereas the induction was inefficient in the same but proline‐deflcient medium [Way‐(‐pro)]. Constitutive AHH activities decreased with increasing culture period. P1450 gene transcripts were slightly expressed when the medium was changed, independently of whether the cells were cultivated in either Way or Way(‐pro), followed by decrease within 24 h and no apparent induction of AHH. However, treatment with Δ1‐pyrroline‐S‐carboxylic acid (P5C), a biosynthetic precursor for proline, dose‐dependently increased basal AHH activities in the cells cultivated in Way‐(‐pro). Benz[a]anthracene induction of AHH in cells cultivated in Way(‐pro) was additively increased in the presence of P5C as much as with proline. Treatment with o‐aminobenzaldehyde, which inactivates P5C, drastically reduced the induced AHH activities in hepatocytes cultivated in either P5C‐added Way (‐pro) or Way medium. Benz[a]anthracene induced both P1450 and P3450 mRNAs. Neither proline nor P5C increased the induced transcripts within 12 h after the start of benz[a]‐anthracene treatment, but the two compounds increased the amounts of P1450 mRNA found at later time points. After treatment with actinomycin D, the half‐life of the induced P1450 mRNA was approximately 12 h, being independent of the presence of either proline or P5C. Our observations suggest that induction of AHH after treatment with polycyclic aromatic hydrocarbon is dependent on proline‐related metabolism which influences the transcriptional process of P1450 gene expression.
机译:在暴露于苯并[a]-蒽后,研究脯氨酸相关的代谢调控后,对原代培养的C57BL / 6小鼠肝细胞中芳烃羟化酶(AHH)及其相应基因CyplA1或P1450在小鼠中的表达进行了研究。当在完全的Waymouth MB752 / 1(Way)中培养细胞时,观察到苯并[a]蒽显着诱导AHH,而在相同但脯氨酸缺乏的培养基[Way-(-pro)]中诱导效率低下。本构AHH活性随培养时间的延长而降低。更换培养基时,P1450基因转录物略有表达,而与是否以Way或Way(-pro)培养的细胞无关,随后在24 h内减少并且没有明显诱导AHH。但是,用Δ1-吡咯啉-S-羧酸(P5C)(脯氨酸的生物合成前体)处理可以剂量依赖性地增加Way-(-pro)培养的细胞中的基础AHH活性。在P5C存在下,苯并[a]蒽在Way(-pro)培养的细胞中对AHH的诱导作用与脯氨酸相加。用灭活P5C的邻氨基苯甲醛处理可大大降低在添加P5C的Way(-pro)或Way培养基中培养的肝细胞中诱导的AHH活性。苯并[a]蒽诱导P1450和P3450 mRNA。在苯并[a]-蒽处理开始后的12小时内,脯氨酸和P5C均未增加诱导的转录本,但是这两种化合物均增加了稍后时间点发现的P1450 mRNA的量。用放线菌素D处理后,诱导的P1450 mRNA的半衰期约为12小时,与脯氨酸或P5C的存在无关。我们的观察结果表明,用多环芳烃处理后AHH的诱导取决于脯氨酸相关的代谢,从而影响P1450基因表达的转录过程。

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