Chen Jie-Gen, Li Xi, Huang Hai-Yan, Liu Hong-Lei, Liu De-Guo, Song Tan-Jing, Ma Chun-Gu, Ma Duan, Song Hou-Yan, Tang Qi-Qun
Key Laboratory of Molecular Medicine, Ministry of Education, Fudan University Shanghai Medical School, Shanghai, PR China.
Biochem Biophys Res Commun. 2006 Sep 1;347(3):821-6. doi: 10.1016/j.bbrc.2006.06.170. Epub 2006 Jul 7.
PAI-1 is expressed and secreted by adipose tissue which may mediate the pathogenesis of obesity-associated cardiovascular complications. Evidence is presented in this report that PAI-1 is not expressed by preadipocyte, but significantly induced during 3T3-L1 adipocyte differentiation and the PAI-1 expression correlates with the induction of peroxisome proliferator-activated receptor gamma (PPARgamma). A peroxisome proliferator responsive element (PPRE)-like cis-element (-206TCCCCCATGCCCT-194) is identified in the mouse PAI-1 gene promoter by electrophoretic mobility shift assay (EMSA) combined with transient transfection experiments; the PPRE-like cis-element forms a specific DNA-protein complex only with adipocyte nuclear extracts, not with preadipocyte nuclear extracts; the DNA-protein complex can be totally competed away by non-labeled consensus PPRE, and can be supershifted with PPARgamma antibody. Mutation of this PPRE-like cis-element can abolish the transactivation of mouse PAI-1 promoter mediated by PPARgamma. Specific PPARgamma ligand Pioglitazone can significantly induce the PAI-1 expression, and stimulate the secretion of PAI-1 into medium.
纤溶酶原激活物抑制因子-1(PAI-1)由脂肪组织表达和分泌,这可能介导肥胖相关心血管并发症的发病机制。本报告提供的证据表明,前脂肪细胞不表达PAI-1,但在3T3-L1脂肪细胞分化过程中PAI-1表达显著上调,且PAI-1表达与过氧化物酶体增殖物激活受体γ(PPARγ)的诱导相关。通过电泳迁移率变动分析(EMSA)结合瞬时转染实验,在小鼠PAI-1基因启动子中鉴定出一个类过氧化物酶体增殖物反应元件(PPRE)顺式元件(-206TCCCCCATGCCCT-194);该类PPRE顺式元件仅与脂肪细胞核提取物形成特异性DNA-蛋白质复合物,而不与前脂肪细胞核提取物形成复合物;该DNA-蛋白质复合物可被未标记的共有PPRE完全竞争掉,并可被PPARγ抗体超迁移。该类PPRE顺式元件的突变可消除由PPARγ介导的小鼠PAI-1启动子的反式激活。特异性PPARγ配体吡格列酮可显著诱导PAI-1表达,并刺激PAI-1分泌到培养基中。