Maldonado Alejandro, He Lin, Game Bryan A, Nareika Alena, Sanders John J, London Steve D, Lopes-Virella Maria F, Huang Yan
Ralph H. Johnson Veterans Affairs Medical Center, Charleston, SC 29401, USA.
J Periodontal Res. 2004 Dec;39(6):415-23. doi: 10.1111/j.1600-0765.2004.00756.x.
It has been well established that patients with diabetes have increased prevalence and severity of periodontal diseases. However, the underlying mechanisms are not well understood. Given that bacterial infection is the primary cause of periodontal disease, we postulated that hyperglycemia may interplay with bacterial virulence factors such as lipopolysaccharide to up-regulate matrix metalloproteinase (MMP), leading to increased periodontal tissue destruction.
We showed that prolonged pre-exposure of U937 histiocytes to high glucose markedly increased lipopolysaccharide-stimulated MMP-1 secretion and mRNA expression. Our results also showed that the effect of high glucose on lipopolysaccharide-induced MMP-1 expression is cell type-specific because no similar response was observed in human gingival fibroblasts. In addition to MMP-1, high glucose also augments lipopolysaccharide-stimulated MMP-7, -8, and -9 mRNA expression. In the investigation of the signaling pathways involved in the enhancement of lipopolysaccharide-induced MMP-1 expression by high glucose, we found that both high glucose and lipopolysaccharide regulate MMP-1 expression through the nuclear factor kappaB (NFkappaB) and mitogen-activated protein kinase (MAPK) cascades.
The present study has shown that pre-exposure to high glucose and subsequent lipopolysaccharide treatment synergistically stimulates MMP-1 expression by mononuclear phagocytes through the NFkappaB and MAPK signaling pathways. This study has thus delineated a pathogenic mechanism that may be involved in the exacerbated periodontal disease in diabetic patients.
糖尿病患者牙周疾病的患病率和严重程度增加,这一点已得到充分证实。然而,其潜在机制尚未完全明确。鉴于细菌感染是牙周疾病的主要病因,我们推测高血糖可能与脂多糖等细菌毒力因子相互作用,上调基质金属蛋白酶(MMP),导致牙周组织破坏增加。
我们发现,U937组织细胞长时间预先暴露于高糖环境下,脂多糖刺激的MMP - 1分泌和mRNA表达显著增加。我们的结果还表明,高糖对脂多糖诱导的MMP - 1表达的影响具有细胞类型特异性,因为在人牙龈成纤维细胞中未观察到类似反应。除了MMP - 1,高糖还增强脂多糖刺激的MMP - 7、 - 8和 - 9的mRNA表达。在研究高糖增强脂多糖诱导的MMP - 1表达所涉及的信号通路时,我们发现高糖和脂多糖均通过核因子κB(NFκB)和丝裂原活化蛋白激酶(MAPK)级联反应调节MMP - 1表达。
本研究表明,预先暴露于高糖环境并随后进行脂多糖处理,可通过NFκB和MAPK信号通路协同刺激单核吞噬细胞表达MMP - 1。因此,本研究阐明了一种可能与糖尿病患者牙周疾病加重有关的致病机制。