Nakajima Mayuka, Honda Tomoyuki, Miyauchi Sayuri, Yamazaki Kazuhisa
Laboratory of Periodontology and Immunology, Division of Oral Science for Health Promotion, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; Division of Periodontology, Department of Oral Biological Science, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Laboratory of Periodontology and Immunology, Division of Oral Science for Health Promotion, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Arch Oral Biol. 2014 Feb;59(2):93-101. doi: 10.1016/j.archoralbio.2013.10.004. Epub 2013 Oct 19.
This study aims to clarify whether gingival fibroblasts produce periostin in response to Th2 cytokines which are elevated in periodontitis lesion and, if so, whether periostin affects the inflammatory response and matrix-protein metabolism.
Human gingival fibroblasts, periodontal ligament cells and the gingival epithelial cell line epi4 were stimulated with interleukin-4 (IL-4), IL-13, tumour necrosis factor-α (TNF-α) and Porphyromonas gingivalis lipopolysaccharide (LPS). Periostin expression was analysed by real-time polymerase chain-reaction (PCR) and Western blotting. The expression of the IL-4 receptor α-chain was evaluated by immunocytochemistry. The effect of periostin on the production of inflammatory cytokines and the expression of matrix protein-related genes was analysed by real-time PCR and enzyme-linked immunosorbent assay (ELISA).
While IL-4 and IL-13 significantly induced periostin production in gingival fibroblasts and periodontal ligament cells, no effect was observed in epi4 cells. No stimulatory effect of TNF-α or P. gingivalis LPS on the production of periostin was observed. The effect of periostin on the production of inflammatory cytokines was weak in gingival fibroblasts; however, little or no effect was observed on periodontal ligament cells or epi4 cells. No significant effect of periostin on the expression of matrix protein-related genes was found.
The results suggest that gingival fibroblasts may be a source of periostin in periodontitis lesions but periostin has only a limited role either in the inflammatory response or in matrix-protein metabolism. Thus, the role of periostin in the cellular interaction between epithelial and mesenchymal cells in gingiva may be distinct from that of skin.
本研究旨在阐明牙龈成纤维细胞是否会因牙周炎病变中升高的Th2细胞因子而产生骨膜蛋白,如果是,骨膜蛋白是否会影响炎症反应和基质蛋白代谢。
用人白细胞介素-4(IL-4)、IL-13、肿瘤坏死因子-α(TNF-α)和牙龈卟啉单胞菌脂多糖(LPS)刺激人牙龈成纤维细胞、牙周膜细胞和牙龈上皮细胞系epi4。通过实时聚合酶链反应(PCR)和蛋白质免疫印迹法分析骨膜蛋白的表达。通过免疫细胞化学评估IL-4受体α链的表达。通过实时PCR和酶联免疫吸附测定(ELISA)分析骨膜蛋白对炎症细胞因子产生和基质蛋白相关基因表达的影响。
虽然IL-4和IL-13显著诱导牙龈成纤维细胞和牙周膜细胞产生骨膜蛋白,但在epi4细胞中未观察到影响。未观察到TNF-α或牙龈卟啉单胞菌LPS对骨膜蛋白产生的刺激作用。骨膜蛋白对牙龈成纤维细胞中炎症细胞因子产生的影响较弱;然而,在牙周膜细胞或epi4细胞中观察到的影响很小或没有影响。未发现骨膜蛋白对基质蛋白相关基因表达有显著影响。
结果表明牙龈成纤维细胞可能是牙周炎病变中骨膜蛋白的来源,但骨膜蛋白在炎症反应或基质蛋白代谢中仅起有限作用。因此,骨膜蛋白在牙龈上皮和间充质细胞之间的细胞相互作用中的作用可能与皮肤不同。