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镰状细胞病患者白细胞中NADPH氧化酶成分的上调及γ干扰素产生增加。

Up-regulation of NADPH oxidase components and increased production of interferon-gamma by leukocytes from sickle cell disease patients.

作者信息

Marçal Lívia E, Dias-da-Motta Péricles M, Rehder Jussara, Mamoni Ronei L, Blotta Maria Heloísa S L, Whitney Constance B, Newburger Peter E, Costa Fernando F, Saad Sara T O, Condino-Neto Antonio

机构信息

Center for Investigation in Pediatrics, Department of Pediatrics, State University of Campinas Medical School, Campinas, Sao Paulo, Brazil.

出版信息

Am J Hematol. 2008 Jan;83(1):41-5. doi: 10.1002/ajh.20991.

DOI:10.1002/ajh.20991
PMID:17654682
Abstract

We have previously demonstrated that mononuclear leukocytes from patients with sickle cell disease (SCD) release higher amounts of superoxide compared with normal controls. The aim of this study was to further study the NADPH oxidase system in these patients by investigating gene expression of NADPH oxidase components, phosphorylation of p47(phox) component, and the release of cytokines related to NADPH oxidase activation in mononuclear leukocytes from patients with SCD. gp91(phox) gene expression was significantly higher in monocytes from SCD patients compared with normal controls (P=0.036). Monocytes from SCD patients showed higher levels of p47(phox) phosphorylation compared with normal controls. INF-gamma release by lymphocytes from SCD patients was significantly higher compared with normal controls, after 48 h culture with phytohemagglutinin (P=0.02). The release of TNF-alpha by monocytes from SCD patients and normal controls was similar after 24 and 48 h culture with lipopolysaccharide (P>0.05). We conclude that monocytes from SCD patients show higher levels of gp91(phox) gene expression and p47(phox) phosphorylation, along with increased IFN-gamma release by SCD lymphocytes. These findings help to explain our previous observation showing the increased respiratory burst activity of mononuclear leukocytes from SCD patients and may contribute to inflammation and tissue damage in these patients.

摘要

我们之前已经证明,与正常对照组相比,镰状细胞病(SCD)患者的单核白细胞释放的超氧化物量更高。本研究的目的是通过研究SCD患者单核白细胞中NADPH氧化酶成分的基因表达、p47(phox)成分的磷酸化以及与NADPH氧化酶激活相关的细胞因子释放,进一步研究这些患者的NADPH氧化酶系统。与正常对照组相比,SCD患者单核细胞中的gp91(phox)基因表达显著更高(P = 0.036)。与正常对照组相比,SCD患者的单核细胞显示出更高水平的p47(phox)磷酸化。在用植物血凝素培养48小时后,SCD患者淋巴细胞释放的INF-γ与正常对照组相比显著更高(P = 0.02)。在用脂多糖培养24小时和48小时后,SCD患者和正常对照组单核细胞释放的TNF-α相似(P>0.05)。我们得出结论,SCD患者的单核细胞显示出更高水平的gp91(phox)基因表达和p47(phox)磷酸化,同时SCD淋巴细胞释放的IFN-γ增加。这些发现有助于解释我们之前的观察结果,即SCD患者单核白细胞的呼吸爆发活性增加,并且可能导致这些患者的炎症和组织损伤。

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