Comprehensive analysis of gene expression in the junctional epithelium by laser microdissection and microarray analysis

被引:30
作者
Hayashi, Y. [1 ,2 ]
Matsunaga, T. [1 ]
Yamamoto, G. [1 ]
Nishii, K. [1 ,2 ]
Usui, M. [2 ]
Yamamoto, M. [2 ]
Tachikawa, T. [1 ]
机构
[1] Showa Univ, Dept Oral Pathol & Diag, Sch Dent, Ohta Ku, Tokyo 1428666, Japan
[2] Showa Univ, Dept Periodontol, Sch Dent, Ohta Ku, Tokyo 1428666, Japan
关键词
junctional epithelium; laser microdissection; microarray; secretory leukocyte protease inhibitor; LEUKOCYTE PROTEASE INHIBITOR; FRESH-FROZEN SECTIONS; ADHESION; PHOSPHORYLATION; LOCALIZATION; SUPPRESSES; MIGRATION; TISSUES; ERP29; CELLS;
D O I
10.1111/j.1600-0765.2010.01276.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background and Objective: The junctional epithelium attaches to the tooth enamel at the dentogingival junction. The attachment mechanisms of the junctional epithelium have been studied histologically, but the molecular functions of the junctional epithelium have not been elucidated. The aim of this study was to perform a comprehensive analysis of gene expression in the junctional epithelium and to search for specific genetic markers of the junctional epithelium. Material and Methods: A comprehensive analysis of genes expressed in the mouse junctional epithelium and oral gingival epithelium was performed using laser microdissection and microarray analysis. To extract high-quality RNA from these tissues, we made frozen sections using a modified film method. Confirmation of the differential expression of selected genes was performed by quantitative real-time PCR and immunohistochemistry. Results: The modified method produced RNA of sufficient quality for microarray analysis. The result of microarray analysis showed that 841 genes were up-regulated in the junctional epithelium compared with the oral gingival epithelium, and five were increased more than 50-fold in the junctional epithelium. These five genes were secretory leukocyte protease inhibitor (Slpi), keratin 17 (Krt17), annexin A1 (Anxa1), myosin light peptide 6 (Myl6) and endoplasmic reticulum protein 29 (Erp29). In particular, Slpi expression in the junctional epithelium was approximately 100-fold higher than in the oral gingival epithelium by real-time PCR. Additionally, immunohistochemistry indicated that the Slpi protein is highly expressed in the junctional epithelium. Conclusion: We developed a method for generating fresh-frozen tissue sections suitable for extraction of good-quality RNA. We determined that Slpi is characteristically expressed in the junctional epithelium. Our results provide a substantial advance in the analysis of gene expression in the junctional epithelium.
引用
收藏
页码:618 / 625
页数:8
相关论文
共 36 条
[1]   Localization of immunoreactive secretory leukocyte protease inhibitor (SLPI) in intestinal mucosa [J].
Bergenfeldt, M ;
Nystrom, M ;
Bohe, M ;
Lindstrom, C ;
Polling, A ;
Ohlsson, K .
JOURNAL OF GASTROENTEROLOGY, 1996, 31 (01) :18-23
[2]   JUNCTIONAL EPITHELIUM EXPRESSES THE INTERCELLULAR-ADHESION MOLECULE ICAM-1 [J].
CRAWFORD, JM ;
HOPP, B .
JOURNAL OF PERIODONTAL RESEARCH, 1990, 25 (04) :254-256
[3]   The Oral Microbial Consortium's Interaction with the Periodontal Innate Defense System [J].
Darveau, Richard P. .
DNA AND CELL BIOLOGY, 2009, 28 (08) :389-395
[4]  
DelCastillo LF, 1996, J PERIODONTAL RES, V31, P36
[5]   Molecular cloning of ERp29, a novel and widely expressed resident of the endoplasmic reticulum [J].
Demmer, J ;
Zhou, CM ;
Hubbard, MJ .
FEBS LETTERS, 1997, 402 (2-3) :145-150
[6]   Commensal bacteria influence innate status within gingival tissues: A pilot study [J].
Dixon, DR ;
Reife, RA ;
Cebra, JJ ;
Darveau, RP .
JOURNAL OF PERIODONTOLOGY, 2004, 75 (11) :1486-1492
[7]   Anti-inflammatory and antimicrobial roles of secretory leukocyte protease inhibitor [J].
Doumas, S ;
Kolokotronis, A ;
Stefanopoulos, P .
INFECTION AND IMMUNITY, 2005, 73 (03) :1271-1274
[8]   Laser capture microdissection [J].
EmmertBuck, MR ;
Bonner, RF ;
Smith, PD ;
Chuaqui, RF ;
Zhuang, ZP ;
Goldstein, SR ;
Weiss, RA ;
Liotta, LA .
SCIENCE, 1996, 274 (5289) :998-1001
[9]   Laminin 5 deposition regulates keratinocyte polarization and persistent migration [J].
Frank, DE ;
Carter, WG .
JOURNAL OF CELL SCIENCE, 2004, 117 (08) :1351-1363
[10]  
Freeman E., 1998, ORAL HISTOLOGY VELOP, V5th, P253