Kido Jun-ichi, Hayashi Noriko, Kataoka Masatoshi, Shinohara Yasuo, Nagata Toshihiko
Department of Periodontology, Faculty of Dentistry, Gadjah Mada University, Yogyakarta, Indonesia.
J Periodontal Res. 2006 Jun;41(3):159-64. doi: 10.1111/j.1600-0765.2005.00845.x.
Calprotectin is composed of two proteins, S100A8 and S100A9, which are S100 family members, and is detected in gingival crevicular fluid and gingival tissue with inflammation. The release and production of calprotectin are regulated by lipopolysaccharides of periodontopathic bacteria and cytokines. Emotional or psychological stress, a risk factor of periodontal disease, is transmitted by stress modulators including norepinephrine and cortisol. The aim of the present study was to investigate the effect of stress on calprotectin expression using norepinephrine and cortisol.
U-937 cells, a human monocytic cell line, were incubated with norepinephrine in the presence or absence of beta- or alpha-adrenergic receptor antagonists, or with cortisol. The expression of S100A8/S100A9 mRNAs was examined by northern blotting and the amount of calprotectin was measured by enzyme-linked immunosorbent assay (ELISA). The DNA binding activity of C/EBPalpha (CCAAT enhancing binding protein), a transcription factor, was examined by electrophoretic mobility shift assay.
Norepinephrine stimulated the expression of S100A8/S100A9 mRNAs via beta-adrenergic receptors in U-937 cells and significantly increased calprotectin production to about 3.6-fold that of the control. However, cortisol had no effect on calprotectin expression at the mRNA and protein levels. Norepinephrine elevated C/EBPalpha DNA binding activity, but cortisol did not increase the activity.
Norepinephrine, a stress modulator, stimulated calprotectin expression in human monocytic cells. Calprotectin expression may be regulated by stress in addition to inflammatory factors.
钙卫蛋白由两种蛋白质S100A8和S100A9组成,它们是S100家族成员,在炎症状态下的龈沟液和牙龈组织中可检测到。钙卫蛋白的释放和产生受牙周病原菌的脂多糖和细胞因子调节。情绪或心理压力是牙周疾病的一个危险因素,可通过包括去甲肾上腺素和皮质醇在内的应激调节因子传递。本研究的目的是使用去甲肾上腺素和皮质醇来研究应激对钙卫蛋白表达的影响。
人单核细胞系U-937细胞在有或无β-或α-肾上腺素能受体拮抗剂存在的情况下与去甲肾上腺素孵育,或与皮质醇孵育。通过Northern印迹法检测S100A8/S100A9 mRNA的表达,并通过酶联免疫吸附测定(ELISA)测量钙卫蛋白的量。通过电泳迁移率变动分析检测转录因子C/EBPα(CCAAT增强结合蛋白)的DNA结合活性。
去甲肾上腺素通过U-937细胞中的β-肾上腺素能受体刺激S100A8/S100A9 mRNA的表达,并使钙卫蛋白的产生显著增加至对照的约3.6倍。然而,皮质醇在mRNA和蛋白质水平上对钙卫蛋白表达没有影响。去甲肾上腺素提高了C/EBPα的DNA结合活性,但皮质醇没有增加该活性。
应激调节因子去甲肾上腺素刺激人单核细胞中钙卫蛋白的表达。除炎症因子外,钙卫蛋白的表达可能还受应激调节。