Hu Y, Davies G E
Department of Pharmaceutical Sciences, College of Pharmacy, South Dakota State University, Brookings, SD 57007, USA.
Phytomedicine. 2009 Sep;16(9):864-73. doi: 10.1016/j.phymed.2009.03.002. Epub 2009 Apr 28.
It is known that a number of transcription factors are key regulators in the complex process of adipocyte differentiation including peroxisome proliferator activated receptor gamma (PPARgamma) and the CCAAT enhancer binding protein alpha (C/EBPalpha). Studies have demonstrated that in pre-adipocyte 3T3-L1 cells constitutive expression of the DNA binding proteins GATA-2 and GATA-3 results in protein/protein interactions with C/EBPalpha resulting in down regulation of PPARgamma and subsequent suppressed adipocyte differentiation with cells trapped at the pre-adipocyte stage. Thus it appears that GATA-2 and GATA-3 are of critical importance in regulating adipocyte differentiation through molecular interactions with PPARgamma and C/EBPalpha. Recent reports suggest that berberine, an isoquinoline derivative alkaloid isolated from many medicinal herbs prevents differentiation of 3T3-L1 cells via a down regulation of PPARgamma and C/EBPalpha expression. The aim of this study was to determine the effect of berberine on GATA-2 and 3 gene and protein expression levels during differentiation of 3T3-L1 cells. MTT (Methylthiazolyldiphenyl-tetrazolium bromide) was used to detect the cytotoxic effects of berberine on the viability of 3T3-L1 cells during proliferation and differentiation. Differentiation of 3T3-L1 cells was monitored by Oil Red O staining and RT-PCR of PPARgamma and C/EBPalpha and the expression of GATA-2 and 3 was determined by RT-PCR and Western Blot. Results show that following treatment with 8microM berberine the mRNA and protein expression levels of GATA-2 and 3 were elevated and accompanied by inhibited adipocyte differentiation. These results may lead to the use of berberine to target the induction of specific genes such as GATA-2 and GATA-3 which affect adipocyte differentiation.
已知多种转录因子是脂肪细胞分化复杂过程中的关键调节因子,包括过氧化物酶体增殖物激活受体γ(PPARγ)和CCAAT增强子结合蛋白α(C/EBPα)。研究表明,在前脂肪细胞3T3-L1细胞中,DNA结合蛋白GATA-2和GATA-3的组成型表达会导致与C/EBPα发生蛋白质/蛋白质相互作用,从而导致PPARγ下调,随后脂肪细胞分化受到抑制,细胞被困在前脂肪细胞阶段。因此,GATA-2和GATA-3似乎在通过与PPARγ和C/EBPα的分子相互作用调节脂肪细胞分化方面至关重要。最近的报道表明,黄连素是一种从多种草药中分离出的异喹啉衍生物生物碱,它通过下调PPARγ和C/EBPα的表达来阻止3T3-L1细胞的分化。本研究的目的是确定黄连素对3T3-L1细胞分化过程中GATA-2和3基因及蛋白表达水平的影响。MTT(噻唑蓝)用于检测黄连素在3T3-L1细胞增殖和分化过程中对细胞活力的细胞毒性作用。通过油红O染色、PPARγ和C/EBPα的RT-PCR监测3T3-L1细胞的分化,并通过RT-PCR和蛋白质印迹法测定GATA-2和3的表达。结果表明,用8μM黄连素处理后,GATA-2和3的mRNA和蛋白表达水平升高,并伴有脂肪细胞分化受到抑制。这些结果可能导致使用黄连素靶向诱导影响脂肪细胞分化的特定基因,如GATA-2和GATA-3。