Department of Oral Biology, Indiana University School of Dentistry, Indianapolis, IN 46202, USA.
J Periodontal Res. 2009 Dec;44(6):704-13. doi: 10.1111/j.1600-0765.2008.01179.x. Epub 2009 May 18.
Cigarette smoke condensate, the particulate matter of cigarette smoke, is composed of thousands of chemicals, including nicotine. Cigarette smoking is a risk factor for periodontal disease. This study investigated the influence of cigarette smoke condensate on the collagen-degrading ability of human gingival fibroblasts and its mechanism.
Human gingival fibroblasts were exposed for 72 h to various concentrations of total particulate matter cigarette smoke condensate. Cell proliferation and cytotoxicity were evaluated using water-soluble tetrazolium-1 and lactate dehydrogenase, respectively. The collagen-degrading ability of human gingival fibroblasts was evaluated in collagen-coated six-well plates. Conditioned media and membrane extracts were collected for zymography and western blot analyses of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs).
Cell proliferation decreased and cytotoxicity increased in human gingival fibroblasts with increasing concentrations of cigarette smoke condensate. Cell proliferation decreased by more than 50% (p < 0.05) when the concentrations of total particulate matter cigarette smoke condensate were above 200 microg/mL, and cytotoxicity increased to more than 30% (p < 0.05) when the concentrations of total particulate matter cigarette smoke condensate were above 400 microg/mL. Cigarette smoke condensate increased the collagen-degrading ability of human gingival fibroblasts, especially at a concentration of 100 microg/mL (1.5-fold increase, p < 0.05) compared with the control. Cigarette smoke condensate increased the production of proMMP-1, proMMP-2, MMP-14 and TIMP-1, and decreased the production of TIMP-2, in conditioned media. Furthermore, compared with the control group, cigarette smoke condensate increased the production of MMP-2, MMP-14 and TIMP-2 in membrane extracts, especially at concentrations of 50-100 microg/mL.
Cigarette smoke condensate affects human gingival fibroblast proliferation and is toxic at total particulate matter cigarette smoke condensate concentrations of >or= 400 microg/mL. Cigarette smoke condensate can increase the collagen-degrading ability of human gingival fibroblasts by altering the production and localization of MMPs and TIMPs.
香烟烟雾凝结物是香烟烟雾的颗粒物,由数千种化学物质组成,包括尼古丁。吸烟是牙周病的一个危险因素。本研究旨在探讨香烟烟雾凝结物对人牙龈成纤维细胞胶原降解能力的影响及其机制。
将人牙龈成纤维细胞暴露于不同浓度的总颗粒物香烟烟雾凝结物中 72 小时。通过水溶性四唑盐和乳酸脱氢酶分别评估细胞增殖和细胞毒性。在胶原包被的六孔板中评估人牙龈成纤维细胞的胶原降解能力。收集条件培养基和膜提取物,用于基质金属蛋白酶(MMPs)和金属蛋白酶组织抑制剂(TIMPs)的明胶酶谱和 Western blot 分析。
随着香烟烟雾凝结物浓度的增加,人牙龈成纤维细胞的增殖减少,细胞毒性增加。当总颗粒物香烟烟雾凝结物浓度高于 200 μg/ml 时,细胞增殖减少超过 50%(p<0.05),当总颗粒物香烟烟雾凝结物浓度高于 400 μg/ml 时,细胞毒性增加超过 30%(p<0.05)。香烟烟雾凝结物增加了人牙龈成纤维细胞的胶原降解能力,特别是在浓度为 100 μg/ml 时(增加 1.5 倍,p<0.05)与对照组相比。香烟烟雾凝结物增加了条件培养基中 proMMP-1、proMMP-2、MMP-14 和 TIMP-1 的产生,并减少了 TIMP-2 的产生。此外,与对照组相比,香烟烟雾凝结物增加了膜提取物中 MMP-2、MMP-14 和 TIMP-2 的产生,特别是在浓度为 50-100 μg/ml 时。
香烟烟雾凝结物影响人牙龈成纤维细胞的增殖,当总颗粒物香烟烟雾凝结物浓度≥400 μg/ml 时具有毒性。香烟烟雾凝结物通过改变 MMPs 和 TIMPs 的产生和定位,增加人牙龈成纤维细胞的胶原降解能力。