华西口腔医学杂志
華西口腔醫學雜誌
화서구강의학잡지
WEST CHINA JOURNAL OF STOMATOLOGY
2015年
1期
6-10
,共5页
郑怡%禤坤%南澜%莫水学
鄭怡%禤坤%南瀾%莫水學
정이%훤곤%남란%막수학
水蛭素%人牙龈成纤维细胞%转化生长因子-β1%碱性成纤维细胞生长因子
水蛭素%人牙齦成纖維細胞%轉化生長因子-β1%堿性成纖維細胞生長因子
수질소%인아간성섬유세포%전화생장인자-β1%감성성섬유세포생장인자
hirudin%human gingival fibroblasts%transforming growth factor-β1%basic fibroblast growth factor
目的:观察水蛭素对人牙龈成纤维细胞(HGFs)碱性成纤维细胞生长因子(bFGF)及转化生长因子-β1(TGF-β1)表达变化的规律,探讨水蛭素影响牙龈改建的可能作用机制。方法体外培养并鉴定HGFs,利用不同浓度的水蛭素分别作用于正常(对照组)和受长期机械外力作用后增生的HGFs(实验组),通过实时定量聚合酶链反应法和免疫细胞化学法检测TGF-β1及bFGF的表达。结果未加入水蛭素时,受长期机械外力作用后,实验组促进HGFs增殖胶原合成的TGF-β1表达升高,而抑制胶原合成的bFGF表达降低(P<0.05)。加入水蛭素干预增生的HGFs后,可正向调节bFGF表达,而负向调节TGF-β1的表达(P<0.05)。结论外力作用干扰了HGFs胶原合成与降解之间的平衡,水蛭素可能通过调节这一平衡而促进牙龈改建过程。
目的:觀察水蛭素對人牙齦成纖維細胞(HGFs)堿性成纖維細胞生長因子(bFGF)及轉化生長因子-β1(TGF-β1)錶達變化的規律,探討水蛭素影響牙齦改建的可能作用機製。方法體外培養併鑒定HGFs,利用不同濃度的水蛭素分彆作用于正常(對照組)和受長期機械外力作用後增生的HGFs(實驗組),通過實時定量聚閤酶鏈反應法和免疫細胞化學法檢測TGF-β1及bFGF的錶達。結果未加入水蛭素時,受長期機械外力作用後,實驗組促進HGFs增殖膠原閤成的TGF-β1錶達升高,而抑製膠原閤成的bFGF錶達降低(P<0.05)。加入水蛭素榦預增生的HGFs後,可正嚮調節bFGF錶達,而負嚮調節TGF-β1的錶達(P<0.05)。結論外力作用榦擾瞭HGFs膠原閤成與降解之間的平衡,水蛭素可能通過調節這一平衡而促進牙齦改建過程。
목적:관찰수질소대인아간성섬유세포(HGFs)감성성섬유세포생장인자(bFGF)급전화생장인자-β1(TGF-β1)표체변화적규률,탐토수질소영향아간개건적가능작용궤제。방법체외배양병감정HGFs,이용불동농도적수질소분별작용우정상(대조조)화수장기궤계외력작용후증생적HGFs(실험조),통과실시정량취합매련반응법화면역세포화학법검측TGF-β1급bFGF적표체。결과미가입수질소시,수장기궤계외력작용후,실험조촉진HGFs증식효원합성적TGF-β1표체승고,이억제효원합성적bFGF표체강저(P<0.05)。가입수질소간예증생적HGFs후,가정향조절bFGF표체,이부향조절TGF-β1적표체(P<0.05)。결론외력작용간우료HGFs효원합성여강해지간적평형,수질소가능통과조절저일평형이촉진아간개건과정。
Objective This study aimed to investigate the effects of hirudin on the expression of transforming growth factor (TGF-β1) and basic fibroblast growth factor (bFGF) in human gingival fibroblasts (HGFs) in vitro, as well to explore its func-tion in the mechanism of gingival remodeling. Methods After culturing was performed with classic tissue-explant method, HGFs were derived from normal gingival and gingival hyperplasia tissues followed by orthodontic treatments with different concentrations of hirudin. The mRNA and protein expression levels of TGF-β1 and bFGF were respectively detected by real time quantity polymerase chain reaction and immunocytochemistry. Results Compared with normal HGFs, TGF-β1 expres-sion promoted collagen synthesis of fibroblasts, whereas bFGF collagen synthesis was decreased in hyperplasia HGFs without hirudin (P<0.05). Hirudin significantly upregulated the expression levels of bFGF but downregulated TGF-β1 in hyperplasia HGFs (P<0.05). Conclusion Orthodontic force may influence the balance of collagen synthesis and degradation in HGFs. Hirudin may modulate the balance of HGF collagen metabolism, thereby promoting gingival remodeling.