Bartold P M
Department of Pathology, University of Adelaide, Australia.
Arch Oral Biol. 1991;36(11):791-7. doi: 10.1016/0003-9969(91)90028-s.
Exposure of gingival fibroblasts to LPS caused a dose-dependent increase in hyaluronate synthesis. Stimulation of hyaluronate synthesis by LPS was significantly greater 24 h after exposure and by 48 h an approx. 50% increase was evident. In parallel, there was an increase in the activity of the hyaluronate synthetase enzyme. Inhibition of PGE2 synthesis by indomethacin abolished the stimulatory effect of LPS on hyaluronate synthesis. Thus, this stimulatory effect of LPS on hyaluronic acid synthesis may be a secondary response to the induction of PGE2. The molecular size of newly synthesized hyaluronate was not affected by LPS. The metabolic changes observed may be a primary response of the cells to bacterial toxins and may aid extracellular matrix repair.
牙龈成纤维细胞暴露于脂多糖会导致透明质酸合成呈剂量依赖性增加。脂多糖刺激透明质酸合成在暴露后24小时显著增强,到48小时时明显增加了约50%。同时,透明质酸合成酶的活性也有所增加。吲哚美辛抑制前列腺素E2合成消除了脂多糖对透明质酸合成的刺激作用。因此,脂多糖对透明质酸合成的这种刺激作用可能是对前列腺素E2诱导的次级反应。新合成的透明质酸的分子大小不受脂多糖影响。观察到的代谢变化可能是细胞对细菌毒素的初级反应,可能有助于细胞外基质修复。