摘要
利用RT-PCR检测不同物质诱导细胞的CYP基因 mRNA的表达水平.在HepG2细胞,TCDD能诱导CYP1A1、CYP1B1及CYP1A2基因表达,CYP1A1、CYP1B1基因比CYP1A2基因更容易被诱导,用AzaC处理后CYP1B1基因表达无改变;在A549细胞和SPC-A1细胞,Azac预处理后增加了TCDD对CYP1家族的诱导.也就是AzaC增加了CYP1A1、CYP1A2和CYP1B1基因表达水平.
The expression levels of mRNA and protein of CYP450 genes were detected by reverse transcription - polymerase chain reaction (RT- PCR). Human CYP1A1, CYP1B1 and mRNAs were constitutively expressed in HepG2 cells and were extensively induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), but CYP1A2 was induced at low level. With AzaC, CYP1 B1 mRNA expression was not activated. In A549 cells and SPC-A1 cells, AzaC pretreatments increased the induction level of the CYP1 family by TCDD. AzaC treatment increased the constitutive expression levels of CYP1A1, CYP1A2 and CYP1B1. Fig 1, Tab 1, Ref 10
出处
《应用与环境生物学报》
CAS
CSCD
北大核心
2007年第3期382-385,共4页
Chinese Journal of Applied and Environmental Biology
基金
国家自然基金资助项目(No.20275012)
湖北省自然科学基金资助项目(2006ABA166)~~