[Comparison of gene expression profile of cementoblasts with periodontal ligament cells in mouse mandible with laser capture microdissection].

Yoshiko Yokoyama
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引用次数: 2

Abstract

Cementum is an essential tissue to maintain tooth function and should be closely correlated to tooth root development and periodontal tissue regeneration. However, detailed features of the periodontium including cementum and specific markers for cementoblasts are unknown. Moreover, the molecular mechanism of periodontal tissue development, homeostasis and regeneration remains unknown. Previous studies have usually examined cementum or periodontalligament (PDL) tissue obtained by manual curettage, resulting in difficulties in isolating pure cementum or PDL. We employed laser capture microdissection (LCM) to isolate cementoblasts and PDL cells from undecalcified frozen sections of murine mandible and to obtain RNA of good quality for subsequent genetic analysis. Over 500 cementoblasts and PDL cells were separately laser captured under microscopy. A bioanalyzer detected peaks of 18S and 28S rRNA both in the laser-dissected cementoblasts and in PDL cells, suggesting that the RNA was of sufficient quality. The RNA samples were amplified due to their small amount and a comparative analysis of mRNA expression by GeneChip showed that about 2,000 genes were differentially expressed between cementoblasts and PDL cells. Both cementoblast-positive and PDL cell-negative genes were serially analyzed by quantitative RT-PCR using RNA samples obtained from mandibles and femurs. Several genes were expressed at higher levels in the mandible than in the femur, suggesting that some might be cementoblast-specific markers. We established a novel experimental system with which to isolate target tissues from single cells in undecalcified frozen sections and to obtain intact RNA. These methodologies could be useful for further investigation of mineralized tissues and to explore tissue-specific factors.

[激光捕获显微解剖小鼠下颌骨牙周韧带细胞成骨质细胞基因表达谱的比较]。
牙骨质是维持牙齿功能的重要组织,与牙根发育和牙周组织再生密切相关。然而,牙周组织的详细特征,包括牙骨质和成牙骨质细胞的特异性标志物是未知的。此外,牙周组织发育、动态平衡和再生的分子机制仍不清楚。以往的研究通常检查手工刮除获得的牙骨质或牙周结石(PDL)组织,导致分离纯牙骨质或PDL的困难。我们采用激光捕获显微解剖(LCM)从未钙化的小鼠下颌骨冷冻切片中分离成骨水泥细胞和PDL细胞,并获得高质量的RNA用于随后的遗传分析。激光显微镜下分别捕获500多个成水泥细胞和PDL细胞。生物分析仪在激光解剖的成水泥细胞和PDL细胞中检测到18S和28S rRNA峰,表明RNA具有足够的质量。由于RNA样本数量较少,因此对其进行了扩增,通过GeneChip对mRNA表达的比较分析显示,在成水泥细胞和PDL细胞之间约有2000个基因存在差异表达。利用从下颌骨和股骨中获得的RNA样本,通过定量RT-PCR对成水泥细胞阳性和PDL细胞阴性基因进行了序列分析。有几个基因在下颌骨中的表达水平高于股骨,这表明其中一些可能是成水泥细胞特异性标记。我们建立了一种新的实验系统,可以从未钙化的冷冻切片中分离出单细胞的靶组织,并获得完整的RNA。这些方法可用于进一步研究矿化组织和探索组织特异性因素。
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