...
首页> 外文期刊>Drug metabolism and pharmacokinetics. >Effects of hypoxia-inducible factor-1α chemical stabilizer, CoCl 2 and hypoxia on gene expression of CYP3As in human fetal liver cells
【24h】

Effects of hypoxia-inducible factor-1α chemical stabilizer, CoCl 2 and hypoxia on gene expression of CYP3As in human fetal liver cells

机译:缺氧诱导因子-1α化学稳定剂,CoCl 2和缺氧对人胎肝细胞CYP3A基因表达的影响

获取原文
获取原文并翻译 | 示例
           

摘要

Distinctive response patterns of CYP3A4 and CYP3A7 to cobalt chloride (CoCl 2) in human fetal liver (HFL) cells were observed and compared with those under hypoxic conditions. The expression levels of CYP3A4 and CYP3A7 mRNAs were decreased by CoCl2 and hypoxia, although significance could not be determined in HFL cells cultured under 3% O 2. The hypoxia-inducible factor-1α (HIF-1α) protein content in HFL cells was significantly increased by CoCl 2 and 3% O 2. Transcriptional activities of CYP3A4 and CYP3A7 were not altered by 3% O 2 when reporter plasmids containing the promoter region ranging up to about 10 kb and 12 kb upstream, respectively, were transfected into HFL cells, although the activity was significantly suppressed by CoCl2. These results suggested that the mechanisms controlling CYP3A gene expression of HIF-1α chemical stabilizer in fetal hepatocytes might be different from those in adult hepatocytes, and that HIF-1α is not directly involved in regulation of CYP3A4 or CYP3A7 expression.
机译:观察到人胎肝(HFL)细胞中CYP3A4和CYP3A7对氯化钴(CoCl 2)的独特响应模式,并将其与低氧条件下的响应模式进行比较。 CYP3A4和CYP3A7 mRNA的表达由于CoCl2和低氧而降低,尽管在3%O 2下培养的HFL细胞中没有确定显着性。HFL细胞中的缺氧诱导因子-1α(HIF-1α)蛋白含量显着当将含有分别在上游约10 kb和12 kb左右的启动子区域的报告质粒转染到HFL细胞中时,CYP3A4和CYP3A7的转录活性不会被3%O 2改变。尽管该活性被CoCl 2显着抑制。这些结果提示,胎儿肝细胞中HIF-1α化学稳定剂的CYP3A基因表达调控机制可能与成年肝细胞中CYP3A基因表达调控机制不同,且HIF-1α不直接参与CYP3A4或CYP3A7表达的调控。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号