Tang Qi-Qun, Zhang Jiang-Wen, Daniel Lane M
Biological Chemistry, Johns Hopkins University School of Medicine, 725 N. Wolfe Street Baltimore, MD 21205, USA.
Biochem Biophys Res Commun. 2004 May 21;318(1):213-8. doi: 10.1016/j.bbrc.2004.04.017.
Treatment of 3T3-L1 preadipocytes with differentiation inducers triggers a cascade in which C/EBPbeta is rapidly expressed, followed by C/EBPalpha and PPARgamma. C/EBPalpha and PPARgamma then activate the expression of adipocyte genes that produce the differentiated phenotype. Circumstantial evidence indicates that C/EBPbeta activates transcription of the C/EBPalpha and PPARgamma genes, both of which possess C/EBP regulatory elements in their proximal promoters. Although C/EBPbeta is expressed immediately upon induction of differentiation, acquisition of DNA binding activity is delayed for approximately 14h. Chromatin immunoprecipitation (ChIP) analysis conducted 24h after induction revealed that C/EBPbeta binds to C/EBP regulatory elements in the proximal promoters of the C/EBPalpha and PPARgamma genes. ChIP analysis showed that after an additional delay C/EBPalpha binds to its own promoter and to the promoters of the PPARgamma and 422/aP2 genes. These findings support the view that once expressed, C/EBPalpha is responsible for maintaining the expression of PPARgamma, and C/EBPalpha, as well as adipocyte proteins (e.g., 422/aP2) in the terminally differentiated state. Together these findings provide compelling evidence that C/EBPbeta, C/EBPalpha, and PPARgamma participate in a cascade during adipogenesis.
用分化诱导剂处理3T3 - L1前脂肪细胞会引发一系列反应,其中C/EBPβ迅速表达,随后是C/EBPα和PPARγ。C/EBPα和PPARγ随后激活产生分化表型的脂肪细胞基因的表达。间接证据表明,C/EBPβ激活C/EBPα和PPARγ基因的转录,这两个基因在其近端启动子中都具有C/EBP调节元件。尽管在诱导分化后C/EBPβ立即表达,但其DNA结合活性的获得延迟约14小时。诱导后24小时进行的染色质免疫沉淀(ChIP)分析表明,C/EBPβ与C/EBPα和PPARγ基因近端启动子中的C/EBP调节元件结合。ChIP分析表明,在进一步延迟后,C/EBPα与其自身的启动子以及PPARγ和422/aP2基因的启动子结合。这些发现支持这样一种观点,即一旦表达,C/EBPα负责维持PPARγ以及处于终末分化状态的C/EBPα和脂肪细胞蛋白(如422/aP2)的表达。这些发现共同提供了令人信服的证据,表明C/EBPβ、C/EBPα和PPARγ在脂肪生成过程中参与了一个级联反应。