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牙周炎患者龈沟液中溶血磷脂酸水平较低,原因是可溶性溶血磷脂酶活性高:其对牙周炎导致的牙槽骨丢失具有潜在的保护作用。

A low level of lysophosphatidic acid in human gingival crevicular fluid from patients with periodontitis due to high soluble lysophospholipase activity: Its potential protective role on alveolar bone loss by periodontitis.

机构信息

Department of Pharmaceutical Health Chemistry, Institute of Biomedical Sciences, Tokushima University Graduate School, Shomachi, Tokushima 770-8505, Japan.

Department of Periodontology and Endodontology, Institute of Biomedical Sciences, Tokushima University Graduate School, Kuramoto, Tokushioma 770-8504, Japan.

出版信息

Biochim Biophys Acta Mol Cell Biol Lipids. 2020 Jul;1865(7):158698. doi: 10.1016/j.bbalip.2020.158698. Epub 2020 Mar 13.

Abstract

We previously detected a submicromolar concentration of lysophosphatidic acid (LPA) in human saliva. Here, we compare LPA concentrations in human gingival crevicular fluid (GCF) from patients with periodontitis and healthy controls, and examine how the local LPA levels are regulated enzymatically. The concentrations of LPA and its precursor lysophospholipids in GCF was measured by liquid chromatography-tandem mass spectrometry. The LPA-producing and LPA-degrading enzymatic activities were measured by quantifying the liberated choline and free fatty acid, respectively. The concentration of LPA in GCF of periodontitis patients was lower than that of healthy controls, due to higher soluble lysophospholipase activity toward LPA. LPA was found to prevent survival of Sa3, a human gingival epithelium-derived tumor cell line, activate Sa3 through Ca mobilization, and release interleukin 6 from Sa3 in vitro. Furthermore, local injection of LPA into the gingiva attenuated ligature-induced experimental alveolar bone loss induced by oral bacteria inoculation in a rat model of periodontitis in vivo. A high concentration of LPA in human GCF is necessary to maintain normal gingival epithelial integrity and function, protecting the progression of periodontitis.

摘要

我们之前在人唾液中检测到亚毫摩尔浓度的溶血磷脂酸(LPA)。在这里,我们比较了牙周炎患者和健康对照者龈沟液(GCF)中的 LPA 浓度,并研究了局部 LPA 水平如何通过酶促作用进行调节。通过液相色谱-串联质谱法测量 GCF 中 LPA 和其前体溶血磷脂的浓度。通过定量释放的胆碱和游离脂肪酸,分别测量 LPA 产生和 LPA 降解的酶活性。由于对 LPA 的可溶性溶血磷脂酶活性较高,牙周炎患者 GCF 中的 LPA 浓度低于健康对照组。发现 LPA 可防止人牙龈上皮来源的肿瘤细胞系 Sa3 的存活,通过钙动员激活 Sa3,并在体外从 Sa3 释放白细胞介素 6。此外,局部注射 LPA 到牙龈可减轻大鼠牙周炎模型中口腔细菌接种引起的结扎诱导的实验性牙槽骨丢失。人 GCF 中的高浓度 LPA 对于维持正常的牙龈上皮完整性和功能是必需的,可保护牙周炎的进展。

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