Wenke Ann-Kathrin, Grässel Susanne, Moser Markus, Bosserhoff Anja K
Institute of Pathology, University Regensburg, Germany.
FEBS J. 2009 May;276(9):2494-504. doi: 10.1111/j.1742-4658.2009.06973.x. Epub 2009 Mar 16.
Activating enhancer-binding protein (AP)-2epsilon was previously described as a new regulator of integrin alpha(10) expression in cartilage. In this study, we analyzed the expression of AP-2epsilon in differentiated chondrocytes and in human mesenchymal stem cells (HMSCs), which have been differentiated into chondrocytes in vitro. AP-2epsilon is predominantly expressed during the late stages of chondrocyte differentiation, mainly in early hypertrophic cartilage, consistent with immunohistochemical stainings of mouse embryo sections. Furthermore, osteoarthritic chondrocytes, resembling a hypertrophic phenotype, have high AP-2epsilon levels. The AP-2epsilon promoter harbors binding sites for the transcription factors AP-2alpha and Sox9. Both transcription factors strongly activate AP-2epsilon expression in a cooperative manner in the chondrosarcoma cell line SW1353. The inhibition of Sox9 expression by small interfering RNA resulted in decreased AP-2epsilon expression. In addition, direct interaction of Sox9 with the AP-2epsilon promoter could be confirmed by chromatin immunoprecipitation and electromobility shift assays. This is the first study to prove the direct regulation of AP-2epsilon by the transcription factor Sox9, and to indicate that AP-2epsilon potentially has an important role as a modulator of hypertrophic cartilage.
激活增强子结合蛋白(AP)-2ε先前被描述为软骨中整合素α(10)表达的一种新调节因子。在本研究中,我们分析了AP-2ε在分化的软骨细胞以及体外已分化为软骨细胞的人间充质干细胞(HMSC)中的表达情况。AP-2ε主要在软骨细胞分化的后期表达,主要存在于早期肥大软骨中,这与小鼠胚胎切片的免疫组织化学染色结果一致。此外,呈现肥大表型的骨关节炎软骨细胞具有较高的AP-2ε水平。AP-2ε启动子含有转录因子AP-2α和Sox9的结合位点。在软骨肉瘤细胞系SW1353中,这两种转录因子以协同方式强烈激活AP-2ε的表达。用小干扰RNA抑制Sox9的表达导致AP-2ε表达下降。此外,通过染色质免疫沉淀和电泳迁移率变动分析可以证实Sox9与AP-2ε启动子的直接相互作用。这是首次证明转录因子Sox9对AP-2ε进行直接调控的研究,并表明AP-2ε可能作为肥大软骨的调节因子发挥重要作用。