Keratinocyte growth factor-1 expression in healthy and diseased human periodontal tissues

被引:17
作者
Li, M [1 ]
Firth, JD [1 ]
Putnins, EE [1 ]
机构
[1] Univ British Columbia, Fac Dent, Dept Oral Biol & Med Sci, Lab Periodontol Biol, Vancouver, BC V6T 1Z3, Canada
关键词
epithelium; keratinocyte growth factor-1; laser dissection; periodontitis;
D O I
10.1111/j.1600-0765.2004.00780.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives: Keratinocyte growth factor-1 (KGF-1) is up-regulated in chronic inflammation and specifically stimulates epithelial cell proliferation by signaling through the epithelial-specific keratinocyte growth factor receptor (KGFR). We examined KGF-1 and KGFR protein and gene expression in healthy and diseased periodontal tissues. Methods: Tissues were collected from patients with periodontal health or disease, immediately frozen and stained for KGF-1 and KGFR protein expression. Laser capture microdissection of epithelial and connective tissue cells with reverse transcription-polymerase chain reaction (RT-PCR) examined KGF-1 and KGFR gene expression profiles and enzymatic digestion with heparitinase, chondroitinase ABC or pre-treatment with suramin examined epithelial surface molecule interactions with KGF-1. Results: In tissues collected from healthy patients, KGF-1 protein localized to areas of junctional and basal oral epithelial cells and was significantly increased in periodontal pocket epithelium (p < 0.01) and in the oral epithelium (p < 0.05) of disease-associated tissues. KGFR localized to the junctional and the parabasal cells of oral epithelium, with the relative staining intensity being increased in disease-associated pocket epithelium (p < 0.05). Laser capture microdissection with RT-PCR confirmed KGF-1 and KGFR were specifically expressed by connective tissue and epithelium, respectively. KGF-1 localization to epithelial cells was largely eliminated by suramin pre-treatment, indicating interaction with the KGFR. Conclusions: KGF-1 and KGFR proteins are expressed in healthy periodontal tissues but significantly increased in diseased periodontal tissues. We hypothesize up-regulation of KGF-1 and KGFR protein associated with disease regulates epithelial cell behavior associated with onset and progression of periodontal pocket formation.
引用
收藏
页码:118 / 128
页数:11
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