...
首页> 外文期刊>Molecular and Biochemical Parasitology >Leishmania lipophosphoglycan activates the transcription factor activating protein 1 in J774A.1 macrophages through the extracellular signal-related kinase (ERK) and p38 mitogen-activated protein kinase.
【24h】

Leishmania lipophosphoglycan activates the transcription factor activating protein 1 in J774A.1 macrophages through the extracellular signal-related kinase (ERK) and p38 mitogen-activated protein kinase.

机译:利什曼原虫脂磷酸聚糖通​​过细胞外信号相关激酶(ERK)和p38促分裂原活化蛋白激酶激活J774A.1巨噬细胞中的转录因子激活蛋白1。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Leishmania donovani is an obligatory intracellular pathogen that resides and multiplies in the phagolysosomes of macrophages. The outcome of this infection depends on the balance between the host ability to activate macrophage killing and the parasite ability to suppress or evade this host immune response. Lipophosphoglycan (LPG) glycoconjugate, the surface molecule of the protozoan parasite is a virulence determinant and a major parasite molecule involved in this process. In this study, we examined the ability of Leishmania and its surface molecule, lipophosphoglycan to activate activating protein 1 (AP-1) through the mitogen-activated protein kinase (MAPK) cascade. We report here that the Leishmania surface molecule, lipophosphoglycan stimulates the simultaneous activation of all three classes of MAP kinases, extracellular signal-related kinases (ERKs), the c-jun amino-terminal kinase (JNK) and the p38 MAP kinase with differential kinetics in J774A.1 macrophage cell line. Furthermore, both L. donovani and its surface molecule lipophosphoglycan resulted in a dose- and time-dependent induction of AP-1 DNA-binding activity. We have also shown a dose-dependent increase of AP-1 binding activity in both low and high virulent strains of parasite. The use of inhibitors selective for ERK (PD98059) and p38 (SB203580) pathway showed that pre-incubation of cells with either SB203580 or PD98059 affected the binding activity of AP-1 suggesting that both p38 and ERK MAP kinase activation appear to be necessary for AP-1 activation by LPG. Lipophosphoglycan induced IL-12 production and generation of nitric oxide in murine macrophages. These results demonstrate that L. donovani LPG activates pro-inflammatory, endotoxin-like response pathway in J774A.1 macrophages and the interaction may play a pivotal role in the elimination of the parasite.
机译:利什曼原虫是一种必需的细胞内病原体,其驻留并在巨噬细胞的吞噬溶酶体中繁殖。这种感染的结果取决于宿主激活巨噬细胞杀死的能力与抑制或逃避宿主免疫反应的寄生虫能力之间的平衡。脂蛋白聚糖(LPG)糖缀合物,是原生动物寄生虫的表面分子,是毒力决定因素,也是参与此过程的主要寄生虫分子。在这项研究中,我们检查了利什曼原虫及其表面分子脂磷酸聚糖通​​过有丝分裂原激活的蛋白激酶(MAPK)级联激活激活蛋白1(AP-1)的能力。我们在这里报告,利什曼原虫表面分子脂磷酸聚糖刺激所有三类MAP激酶,细胞外信号相关激酶(ERK),c-jun氨基末端激酶(JNK)和p38 MAP激酶同时激活,并具有不同的动力学在J774A.1巨噬细胞系中。此外,杜氏乳酸杆菌及其表面分子脂磷酸聚糖均导致剂量依赖性和时间依赖性的AP-1 DNA结合活性的诱导。我们还显示了低毒力和高毒力的寄生虫菌株中AP-1结合活性的剂量依赖性增加。对ERK(PD98059)和p38(SB203580)途径具有选择性的抑制剂的使用表明,将带有SB203580或PD98059的细胞预孵育会影响AP-1的结合活性,这表明p38和ERK MAP激酶激活似乎是必需的。 LPG激活AP-1。脂质磷酸聚糖诱导小鼠巨噬细胞中IL-12的产生和一氧化氮的产生。这些结果表明,多诺氏乳酸杆菌LPG可激活J774A.1巨噬细胞中促炎性内毒素样反应途径,并且该相互作用可能在消除寄生虫中起关键作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号