首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Lipoteichoic Acid of Enterococcus faecalis Inhibits the Differentiation of Macrophages into Osteoclasts
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Lipoteichoic Acid of Enterococcus faecalis Inhibits the Differentiation of Macrophages into Osteoclasts

机译:粪肠球菌的脂磷壁酸抑制巨噬细胞分化为破骨细胞

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Introduction: Enterococcus faecalis is associated with persistent endodontic infection and refractory apical periodontitis. Recently, we have shown that heat killed E. faecalis attenuates osteoclast differentiation. Because lipoteichoic acid (LTA) is a major virulence factor of gram-positive bacteria, we investigated the effect of LTA from E. faecalis (EfLTA) on osteoclast differentiation. Methods: EfLTA was purified through organic solvent extraction, hydrophobic interaction column chromatography, and ion exchange column chromatography. Bone marrow cells from C57BL/6 or Toll-like receptor 2 deficient mice were incubated with macrophage colony-stimulating factor (M-CSF) for 5 days to generate macrophages (bone marrow derived macrophages [BMMs]). The cells were differentiated into osteoclasts with M-CSF and receptor activator of NF-kappa B ligand (RANKL) in the presence or absence of EfLTA. The degree of osteoclast differentiation was determined by tartrate-resistant acid phosphatase staining. The expression of NFATc1 and c-Fos transcription factors was determined by Western blotting. A phagocytosis assay was performed by measuring the uptake of carboxyfluorescein diacetate succinimidyl ester stained E. faecalis. An enzyme-linked immunosorbent assay was used to determine the amount of cytokines and chemokines. Results: When BMMs were treated with EfLTA, osteoclast differentiation was attenuated. EfLTA inhibited the RANKL-induced expression of NFATc1 and c-Fos. EfLTA inhibition of osteoclast differentiation was not observed in TLR2-deficient BMMs. In addition, EfLTA sustained the phagocytic capacity of BMMs even after the differentiation into osteoclasts, whereas it induced the expression of inflammatory cytokines and chemokines. Conclusions: EfLTA inhibits the differentiation of macrophages into osteoclasts and thereby maintains the phagocytic and inflammatory capacities of macrophages, potentially contributing to refractory apical periodontitis.
机译:简介:粪肠球菌与持续性牙髓感染和难治性根尖性牙周炎有关。最近,我们已经显示,热杀死的粪肠球菌减弱了破骨细胞的分化。因为脂磷壁酸(LTA)是革兰氏阳性细菌的主要毒力因子,所以我们研究了粪肠球菌(EfLTA)的LTA对破骨细胞分化的影响。方法:通过有机溶剂萃取,疏水作用柱色谱和离子交换柱色谱法纯化EfLTA。将C57BL / 6或Toll样受体2缺陷型小鼠的骨髓细胞与巨噬细胞集落刺激因子(M-CSF)孵育5天,以生成巨噬细胞(骨髓来源的巨噬细胞[BMM])。在存在或不存在EfLTA的情况下,将细胞用M-CSF和NF-κB配体的受体激活剂(RANKL)分化为破骨细胞。通过抗酒石酸酸性磷酸酶染色来确定破骨细胞的分化程度。通过蛋白质印迹法测定NFATc1和c-Fos转录因子的表达。通过测量羧基荧光素二乙酸酯琥珀酰亚胺酯染色的粪肠球菌的摄取来进行吞噬作用测定。酶联免疫吸附测定法用于确定细胞因子和趋化因子的量。结果:当用EfLTA治疗BMM时,破骨细胞分化减弱。 EfLTA抑制RANKL诱导的NFATc1和c-Fos的表达。在缺乏TLR2的BMM中未观察到EfLTA对破骨细胞分化的抑制作用。此外,EfLTA甚至在分化为破骨细胞后仍能维持BMM的吞噬能力,​​而EfLTA却诱导了炎症细胞因子和趋化因子的表达。结论:EfLTA抑制巨噬细胞向破骨细胞的分化,从而维持巨噬细胞的吞噬和炎性功能,可能导致难治性根尖周炎。

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