首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Heat-killed Enterococcus faecalis alters nitric oxide and CXCL12 production but not CXCL8 and CCL3 production by cultured human dental pulp fibroblasts.
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Heat-killed Enterococcus faecalis alters nitric oxide and CXCL12 production but not CXCL8 and CCL3 production by cultured human dental pulp fibroblasts.

机译:加热杀死的粪肠球菌可改变人牙髓成纤维细胞产生的一氧化氮和CXCL12的产量,但不会改变CXCL8和CCL3的产量。

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INTRODUCTION: Fibroblasts are the most abundant cells in dental pulp. To investigate their capacity to produce the chemokines CCL3, CXCL8, and CXCL12 as well as nitric oxide (NO), we evaluated the production of these mediators in supernatants of cultured human dental pulp fibroblasts (HDPF) stimulated by heat-killed Enterococcus faecalis (HKEF). METHODS: Primary cultures of HDPF were stimulated with medium alone or HKEF (1:1, 10:1, or 100:1 bacteria:fibroblast) for 1, 6, and 24 hours. Chemokines and NO were assessed through enzyme-linked immunosorbent assay and Griess reaction, respectively. Statistical analysis was performed by using analysis of variance and Tukey post test. RESULTS: CCL3 was not detected, whereas constitutive CXCL8 was not affected. Production of CXCL12 was increased at 1 and 6 hours, and NO was increased at the concentration of 1:1 bacteria:fibroblast at 24 hours. Viability and proliferation assays did not reveal cell number differences. CONCLUSIONS: These findings demonstrate that heat-killed E. faecalis is able to increase production of CXCL12 and NO by HDPF.
机译:简介:成纤维细胞是牙髓中最丰富的细胞。为了研究其产生趋化因子CCL3,CXCL8和CXCL12以及一氧化氮(NO)的能力,我们评估了由热杀死粪便肠球菌(HKEF)刺激的人类牙髓成纤维细胞(HDPF)上清液中这些介体的产生。 )。方法:用单独的培养基或HKEF(1:1、10:1或100:1细菌:成纤维细胞)刺激HDPF的原代培养1、6和24小时。通过酶联免疫吸附试验和格里斯反应分别评估趋化因子和NO。通过使用方差分析和Tukey Post检验进行统计分析。结果:未检测到CCL3,而本构CXCL8不受影响。在1小时和6小时,CXCL12的产量增加,在24小时时,1:1细菌:成纤维细胞的浓度下NO含量增加。活力和增殖测定未显示细胞数量差异。结论:这些发现表明,热灭活的粪肠球菌能够通过HDPF增加CXCL12和NO的产生。

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