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首页> 外文期刊>Archives of dermatological research. >Streptococcus sanguinis and the sera of patients with Beh?et's disease stimulate membrane expression of α-enolase in human dermal microvascular endothelial cells
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Streptococcus sanguinis and the sera of patients with Beh?et's disease stimulate membrane expression of α-enolase in human dermal microvascular endothelial cells

机译:血链球菌和贝氏病患者的血清刺激人真皮微血管内皮细胞中α-烯醇化酶的膜表达

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The glycolytic enzyme α-enolase is a plasminogen-binding protein that is generally found in the cytosolic compartment. However, α-enolase can also be expressed on cell surfaces following an inflammatory stimulus via an unknown mechanism. We investigated the effects of Streptococcus sanguinis (S. sanguinis) and the sera of patients with Beh?et's disease (BD) on the expression and distribution of α-enolase in human dermal microvascular endothelial cells (HDMECs). HDMECs were stimulated with cultured S. sanguinis and the sera of active BD patients. HDMECs incubated for 6, 12 or 24 h were harvested, and the membrane and cytoplasmic fractions of proteins were extracted. The expression and distribution of α-enolase were analyzed using subcellular fractionation and immunoblotting. Subcellular localization of α-enolase was also assessed by immunocytochemistry. S. sanguinis stimulated the expression of α-enolase in the membranous compartment of HDMECs in a dose-dependent manner. This pattern was also observed in HDMECs incubated with BD patients' sera. Although incubation of HDMECs with sera from healthy controls increased membrane expression of α-enolase, incubation with BD sera resulted in earlier and higher expression of this glycoprotein in the cellular membrane of HDMECs. Immunocytochemistry revealed strong immunostaining of α-enolase in the cytoplasm and cytoplasmic membrane of HDMECs incubated with S. sanguinis or BD patients' sera. In conclusions, these results indicate that S. sanguinis infection and the sera of BD patients with active disease are inflammatory stimuli that can induce membranous α-enolase expression in endothelial cells. Membrane-expressed α-enolase could potentially react with anti-α-enolase antibodies in BD patients' sera, resulting in increased inflammation.
机译:糖酵解酶α-烯醇酶是纤溶酶原结合蛋白,通常存在于胞质区室。但是,α-烯醇酶也可以通过未知机制在炎症刺激后在细胞表面表达。我们调查了链球菌血红蛋白(S. sanguinis)和贝希特氏病(BD)患者的血清对人皮肤微血管内皮细胞(HDMEC)中α-烯醇化酶表达和分布的影响。 HDMECs由培养的血红链球菌和活跃BD患者的血清刺激。收获孵育6、12或24小时的HDMEC,并提取蛋白质的膜和细胞质级分。使用亚细胞分级分离和免疫印迹分析α-烯醇酶的表达和分布。还通过免疫细胞化学评估了α-烯醇化酶的亚细胞定位。血红链霉菌以剂量依赖性方式刺激HDMEC的膜区室中α-烯醇酶的表达。在与BD患者血清孵育的HDMEC中也观察到了这种模式。尽管将HDMEC与健康对照的血清一起孵育会增加α-烯醇酶的膜表达,但与BD血清一起孵育会导致该糖蛋白在HDMEC的细胞膜中更早,更高的表达。免疫细胞化学显示,在与血红链球菌或BD患者血清孵育的HDMEC的细胞质和细胞质膜中,α-烯醇酶具有很强的免疫染色作用。总之,这些结果表明,血红链球菌感染和患有活动性疾病的BD患者的血清是炎性刺激,可诱导内皮细胞膜性α-烯醇酶表达。膜表达的α-烯醇酶可能与BD患者血清中的抗α-烯醇酶抗体发生反应,从而导致炎症增加。

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