Shapira L, Houri Y, Barak V, Halabi A, Soskolne W A, Stabholz A
Department of Periodontics, Hebrew University, Hadassah Faculty of Dental Medicine, Jerusalem, Israel.
J Periodontol. 1996 Jul;67(7):682-7. doi: 10.1902/jop.1996.67.7.682.
Monocyte inflammatory cytokines, such as TNF alpha and IL-1 beta, have been implicated in the pathogenesis of periodontal destruction. The present study was designed to test the ability of extracts of cementum from periodontally diseased teeth to induce the secretion of these mediators by monocytes, to evaluate the role of adsorbed endotoxin in this process, and to test the effect of cementum conditioning with tetracycline on the monocyte response. Human monocytes were incubated with varying concentrations of cementum extracts, and TNF alpha and IL-1 beta levels in the media were measured. The results showed that while extracts of healthy cementum had no effect on monocyte secretion, concentration as low as 0.5 mg/ml of cementum from diseased sites raised the levels of TNF alpha and IL-1 beta secretion 10-fold. This response was dose-dependent. Diseased cementum were found to contain 1.5 ng/mg endotoxin, while endotoxin was not detectable in the extracts of the healthy cementum. However, neutralization of the endotoxin by polymyxin B only partially reduced the monocyte secretory response by 50 to 70%, suggesting that other factors in the extracts are also involved in monocyte stimulation. To simulate the effect of root conditioning, cementum was first agitated in a tetracycline or control solution prior to its extraction in media. Pretreatment of diseased cementum with tetracycline (50 mg/ml) was found to block the secretion of TNF alpha from cementum-stimulated monocytes. Pretreatment of the diseased cementum with 10 mg/ml tetracycline was not more effective than saline and HCI controls, with all treatments reducing cytokine secretion by approximately 80%. The direct addition of tetracycline to cementum-stimulated monocyte culture was found to block TNF alpha secretion in a dose dependent manner. The results suggest that extracts from diseased cementum are potent stimulators of monocyte secretion, and that endotoxin as well as other factor(s) appear to be involved. These factors are partially extracted by washing and a 10 mg/ml tetracycline solution is not more effective than saline in achieving this goal. In addition, tetracycline was found to be a potent inhibitor of TNF alpha secretion by cementum-stimulated monocytes, suggesting a novel mechanism for this drug in periodontal therapy.
单核细胞炎性细胞因子,如肿瘤坏死因子α(TNFα)和白细胞介素-1β(IL-1β),与牙周组织破坏的发病机制有关。本研究旨在检测牙周病牙齿牙骨质提取物诱导单核细胞分泌这些介质的能力,评估吸附内毒素在此过程中的作用,并检测四环素处理牙骨质对单核细胞反应的影响。将人单核细胞与不同浓度的牙骨质提取物一起孵育,然后检测培养基中TNFα和IL-1β的水平。结果显示,健康牙骨质提取物对单核细胞分泌没有影响,而来自病变部位的牙骨质提取物浓度低至0.5mg/ml时,就能使TNFα和IL-1β的分泌水平提高10倍。这种反应呈剂量依赖性。发现病变牙骨质含有1.5ng/mg内毒素,而健康牙骨质提取物中未检测到内毒素。然而,用多粘菌素B中和内毒素只能使单核细胞分泌反应部分降低50%至70%,这表明提取物中的其他因素也参与了对单核细胞的刺激。为模拟牙根处理的效果,在将牙骨质提取到培养基中之前,先将其在四环素或对照溶液中搅拌。发现用四环素(50mg/ml)预处理病变牙骨质可阻断牙骨质刺激的单核细胞分泌TNFα。用10mg/ml四环素预处理病变牙骨质并不比生理盐水和盐酸对照更有效,所有处理均使细胞因子分泌减少约80%。发现直接向牙骨质刺激的单核细胞培养物中添加四环素可呈剂量依赖性地阻断TNFα分泌。结果表明,病变牙骨质提取物是单核细胞分泌的有效刺激物,内毒素以及其他因素似乎都参与其中。通过冲洗可部分提取这些因素,10mg/ml四环素溶液在实现这一目标方面并不比生理盐水更有效。此外,发现四环素是牙骨质刺激的单核细胞分泌TNFα的有效抑制剂,这提示了该药物在牙周治疗中的一种新机制。