Shin E S, Cho S Y, Lee E H, Lee S J, Chang I S, Lee T R
BioResearch, R&D Center AmorePacific Corporation, 314-1, Bora-Ri, Giheung-Eup, Yongin-Si, Gyeonggi-Do, Korea.
Eur J Nutr. 2006 Mar;45(3):159-64. doi: 10.1007/s00394-005-0576-5. Epub 2005 Dec 20.
Genistein increases CPT1A, a rate-limiting enzyme in the beta-oxidation pathway, enzyme activity by increasing CPT1A transcription in HepG2 cells and, consequently, suppresses high fat induced obesity in C57BL/6J mice. Genistein and daidzein are the most abundant isoflavones in soy.
To investigate the effect of co-treatment of genistein and L-carnitine on CPT1A enzyme activity and to determine whether daidzein also increases CPT1A activity and to establish a cell line that can be used to screen chemicals to regulate CPT1A transcription.
The enzyme activities of CPT1A were determined after HepG2 cells were incubated with 10 microM genistein or 10 microM daidzein or 1 mM L-carnitine or in combination with 10 microM genistein and 1 mM L-carnitine or in combination with 10 microM daidzein and 1 mM L-carnitine. The mRNA expression levels of CPT1A were determined by real time PCR method after HepG2 cells were incubated with 10 microM genistein or 10 microM daidzein. A suggested CPT1A promoter region was cloned from human genomic DNA and the CPT1A promoter-luciferase reporter gene construct was made, and the promoter-reporter gene construct was transfected into human hepatoma cell line Huh7.
The enzyme activity of CPT1A was at least 2.3- fold higher in L-carnitine and genistein co-treated HepG2 cells than either single-agent treated cells. Daidzein also significantly increased the mRNA expression of CPT1A as well as the enzyme activity of CPT1A. A stable Huh7 cell line, which was selected after Huh7 cells were transfected with CPT1A promoter luciferase reporter gene construct, was characterized by confirming that luciferase activity of the cell line can be regulated by genistein and daidzein as well as clofibrate, a well-known CPT1A mRNA up-regulating drug.
Genistein and daidzein can up-regulate CPT1A enzyme activity through up-regulation of CPT1A transcription. Co-treatment of L-carnitine and genistein additively increases CPT1A enzyme activity in HepG2 cells. A stable Huh7 cell line transfected with the CPT1A promoter luciferase reporter gene was established and characterized.
染料木黄酮可增加β-氧化途径中的限速酶CPT1A的酶活性,其通过增加HepG2细胞中CPT1A的转录来实现,进而抑制C57BL/6J小鼠的高脂诱导肥胖。染料木黄酮和黄豆苷元是大豆中含量最丰富的异黄酮。
研究染料木黄酮与L-肉碱联合处理对CPT1A酶活性的影响,确定黄豆苷元是否也能增加CPT1A活性,并建立一种可用于筛选调节CPT1A转录的化学物质的细胞系。
将HepG2细胞与10微摩尔染料木黄酮或10微摩尔黄豆苷元或1毫摩尔L-肉碱孵育,或与10微摩尔染料木黄酮和1毫摩尔L-肉碱联合孵育,或与10微摩尔黄豆苷元与1毫摩尔L-肉碱联合孵育后,测定CPT1A的酶活性。将HepG2细胞与10微摩尔染料木黄酮或10微摩尔黄豆苷元孵育后,通过实时PCR法测定CPT1A的mRNA表达水平。从人基因组DNA中克隆出一段推测的CPT1A启动子区域,构建CPT1A启动子-荧光素酶报告基因构建体,并将该启动子-报告基因构建体转染到人肝癌细胞系Huh7中。
L-肉碱和染料木黄酮联合处理的HepG2细胞中CPT1A的酶活性比单一药物处理的细胞至少高2.3倍。黄豆苷元也显著增加了CPT1A的mRNA表达以及CPT1A的酶活性。在Huh7细胞用CPT1A启动子荧光素酶报告基因构建体转染后筛选出的稳定Huh7细胞系,通过确认该细胞系的荧光素酶活性可被染料木黄酮、黄豆苷元以及氯贝丁酯(一种已知的CPT1A mRNA上调药物)调节来进行表征。
染料木黄酮和黄豆苷元可通过上调CPT1A转录来上调CPT1A酶活性。L-肉碱与染料木黄酮联合处理可使HepG2细胞中CPT1A酶活性呈相加性增加。建立并表征了用CPT1A启动子荧光素酶报告基因转染的稳定Huh7细胞系。