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强力霉素对成纤维细胞黏附于明胶包被表面的影响及其细胞毒性。

The influence of doxycycline of the attachment of fibroblasts to gelatin-coated surfaces and its cytotoxicity.

作者信息

Tsukuda N, Gabler W L

机构信息

Department of Periodontology, School of Dentistry, Hokkaido University, Sapporo, Japan.

出版信息

J Periodontol. 1993 Dec;64(12):1219-24. doi: 10.1902/jop.1993.64.12.1219.

Abstract

Because of their antimicrobial and anti-inflammatory properties, tetracyclines have been used systemically and locally in the treatment of periodontal disease. This study was done to evaluate the influence of doxycycline (Dc), a tetracycline, on fibroblast adherence to a protein coated surface and its cytotoxicity. Periodontal ligament derived fibroblasts (PLDFs) were either: 1) preincubated with Dc (0 to 100 micrograms/ml) and then allowed to adhere to a gelatin-coated surface or 2) adherence was first established and then Dc added to the system. After an appropriate time the number of PLDFs adherent, released, or lysed was estimated by a lactic dehydrogenase (LDH) assay. Preincubation of PLDFs in 25 micrograms Dc/ml or higher concentrations significantly (P < 0.01) reduced the number of adherent cells. Fifty micrograms Dc/ml and higher doses significantly (P < 0.01) increased PLDFs cytotoxicity as measured by LDH release. The same trend was noted if PLDFs were allowed to adhere and then subjected to the drug. Microscopic observation of fluorescein diacetate/propidium iodide-stained cells showed that attached-spread cells pulled in, rounded up, and detached in proportion to the increased dose of Dc and the percentage of red-stained cytotoxic cells rose in a similar manner. The data suggested that Dc can be cytotoxic and may inhibit PLDFs adherence and spread along a substratum.

摘要

由于四环素具有抗菌和抗炎特性,已被全身或局部用于治疗牙周疾病。本研究旨在评估四环素强力霉素(Dc)对成纤维细胞黏附于蛋白包被表面的影响及其细胞毒性。从牙周膜分离出的成纤维细胞(PLDFs)被分为两组:1)先与Dc(0至100微克/毫升)预孵育,然后使其黏附于明胶包被的表面;2)先让细胞黏附,然后向体系中加入Dc。经过适当时间后,通过乳酸脱氢酶(LDH)测定法评估黏附、释放或裂解的PLDFs数量。将PLDFs在25微克/毫升或更高浓度的Dc中预孵育,可显著(P < 0.01)减少黏附细胞的数量。以LDH释放量衡量,50微克/毫升及更高剂量的Dc可显著(P < 0.01)增加PLDFs的细胞毒性。如果让PLDFs先黏附然后再接触药物,也会出现相同趋势。对荧光素二乙酸酯/碘化丙啶染色细胞的显微镜观察表明,随着Dc剂量增加,贴壁铺展的细胞会回缩、变圆并脱离,红色染色的细胞毒性细胞百分比也以类似方式上升。数据表明,Dc具有细胞毒性,可能会抑制PLDFs在基质上的黏附与铺展。

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