Dannewitz Bettina, Edrich Christina, Tomakidi Pascal, Kohl Annette, Gabbert Olaf, Staehle Hans-Jörg, Steinberg Thorsten
Section of Periodontology, Department of Operative Dentistry and Periodontology, University of Heidelberg, Heidelberg, Germany.
J Clin Periodontol. 2006 Jul;33(7):510-6. doi: 10.1111/j.1600-051X.2006.00937.x.
It has been demonstrated that extracellular matrix molecules are involved in cyclosporine-induced gingival overgrowth (GO). However, for many of these molecules, it remains unclear whether their abundance is modulated on the protein and gene expression level.
To contribute to this clarification, we have analysed the protein and mRNA expression of type-I collagen (COL1) and decorin (DC) in native specimens obtained from five patients with GO, and matched normal tissue using indirect immunofluorescence (IIM), in situ hybridization (ISH) and quantitative polymerase chain reaction (PCR).
IIF revealed a largely co-localized although remarkably increased abundance for COL1 and DC in GO. This increase coincided with an up-regulated gene expression observed for both molecules, as detected by ISH and quantitative PCR.
Analysis of our data clearly demonstrates elevated levels for COL1 and DC and shows for the first time in native human tissue that involvement of these genes in GO is not confined to the protein level but also includes the transcriptional level.
已有研究表明细胞外基质分子参与环孢素诱导的牙龈过度生长(GO)。然而,对于其中许多分子,其丰度在蛋白质和基因表达水平上是否受到调节仍不清楚。
为了有助于阐明这一问题,我们使用间接免疫荧光(IIM)、原位杂交(ISH)和定量聚合酶链反应(PCR)分析了从五名GO患者获取的天然标本以及匹配的正常组织中I型胶原蛋白(COL1)和核心蛋白聚糖(DC)的蛋白质和mRNA表达。
间接免疫荧光显示,在GO中,COL1和DC的丰度虽显著增加,但在很大程度上共定位。如ISH和定量PCR检测所示,这种增加与这两种分子观察到的基因表达上调一致。
对我们数据的分析清楚地表明COL1和DC水平升高,并且首次在天然人体组织中表明这些基因参与GO不仅限于蛋白质水平,还包括转录水平。