Laser capture microdissection enables cellular and molecular studies of tooth root development

被引:17
|
作者
Sun, Jian-Xun [1 ,2 ]
Horst, Orapin V. [3 ]
Bumgarner, Roger [4 ]
Lakely, Bryce [5 ]
Somerman, Martha J. [6 ]
Zhang, Hai [7 ]
机构
[1] Sichuan Univ, State Key Lab Oral Dis, Chengdu 610064, Peoples R China
[2] Univ Washington, Dept Periodontol, Seattle, WA 98195 USA
[3] Univ Calif San Francisco, Dept Prevent & Restorat Dent Sci, Div Endodont, San Francisco, CA 94143 USA
[4] Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
[5] Univ Washington, Dept Urol, Seattle, WA 98195 USA
[6] NIAMSD, NIH, Bethesda, MD 20892 USA
[7] Univ Washington, Dept Restorat Dent, Seattle, WA 98195 USA
关键词
gene; laser capture microdissection; microarray; PCR; root; EPITHELIAL-MESENCHYMAL INTERACTIONS; BONE MORPHOGENETIC PROTEINS; RICH AMELOGENIN PEPTIDE; RAT DENTAL FOLLICLE; STEM-CELLS; MACULAR DEGENERATION; GENE-EXPRESSION; FIBULIN-2; EXPRESSION; IN-VITRO; RNA;
D O I
10.1038/ijos.2012.15
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Epithelial-mesenchymal interactions (EMIs) are critical for tooth development. Molecular mechanisms mediating these interactions in root formation is not well understood. Laser capture microdissection (LCM) and subsequent microarray analyses enable large scale in situ molecular and cellular studies of root formation but to date have been hindered by technical challenges of gaining intact histological sections of non-decalcified mineralized teeth or jaws with well-preserved RNA. Here, we describe a new method to overcome this obstacle that permits LCM of dental epithelia, adjacent mesenchyme, odontoblasts and cementoblasts from mouse incisors and molars during root development. Using this method, we obtained RNA samples of high quality and successfully performed microarray analyses. Robust differences in gene expression, as well as genes not previously associated with root formation, were identified. Comparison of gene expression data from microarray with real-time reverse transcriptase polymerase chain reaction (RT-PCR) supported our findings. These genes include known markers of dental epithelia, mesenchyme, cementoblasts and odontoblasts, as well as novel genes such as those in the fibulin family. In conclusion, our new approach in tissue preparation enables LCM collection of intact cells with well-preserved RNA allowing subsequent gene expression analyses using microarray and RT-PCR to define key regulators of tooth root development. International Journal of Oral Science (2012) 4, 7-13; doi:10.1038/ijos.2012.15; published online 16 March 2012
引用
收藏
页码:7 / 13
页数:7
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