首页> 外文期刊>Cytokine >The modulatory role played by TNF-alpha and IL-1 beta in the inflammatory responses induced by carrageenan in the mouse model of pleurisy.
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The modulatory role played by TNF-alpha and IL-1 beta in the inflammatory responses induced by carrageenan in the mouse model of pleurisy.

机译:TNF-α和IL-1β在胸膜炎小鼠模型中由角叉菜胶诱导的炎症反应中发挥调节作用。

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We describe here the modulation caused by intrapleural (i.pl.) injection of the cytokines TNF-alpha and IL-1beta and their specific antibodies in the early (4 h) and late (48 h) inflammatory responses caused by injection of carrageenan (Cg) into the mouse pleural cavity. The antibodies against TNF-alpha and IL-1beta, when injected 30 min prior to Cg, reduced, in a graded and significant manner, both exudation and cell migration in the early (4 h) phase, while they potentiated or had no effect in the late (48 h) phase of Cg response. The natural IL-1 receptor antagonist IL-1RA, given 30 min prior to Cg, reduced the exudation by about 50% and abolished the total and differential cell migration in the early (4 h) and late (48 h) phases of the Cg responses. The i.pl. injection of TNF-alpha or IL-1beta, 5 min prior to Cg, caused graded increase in the exudation of the early (4 h) and late (48 h) phases of the Cg-induced inflammatory responses. In contrast, these treatments markedly reduced the total and differential cell migration at 4 h, while having little or no effect on the late (48 h) phase of the Cg pleurisy. These findings extend previous results and demonstrate that the pro-inflammatory cytokines TNF-alpha and IL-1beta have a critical role in controlling both cell migration and exudation caused by injection of Cg in the mouse pleural cavity. Together, these findings may be relevant to the understanding of the mechanisms involved in airway inflammatory responses. Copyright 2001 Academic Press.
机译:我们在这里描述了由角叉菜胶注射引起的炎症反应的早期(4 h)和晚期(48 h)的胸膜内(i.pl.)细胞因子TNF-alpha和IL-1beta及其特异性抗体的注射引起的调节作用( Cg)进入小鼠胸膜腔。在Cg注射前30分钟,针对TNF-alpha和IL-1beta的抗体以分级且显着的方式减少了早期(4 h)的渗出和细胞迁移,尽管它们增强了或没有作用。 Cg响应的后期(48小时)。在Cg之前30分钟给予天然IL-1受体拮抗剂IL-1RA,可使Cg早期(4 h)和晚期(48 h)的渗出减少约50%,并消除了总的和差异的细胞迁移。回应。 i.pl。在Cg之前5分钟注射TNF-α或IL-1beta会导致Cg诱导的炎症反应早期(4 h)和晚期(48 h)的渗出逐渐增加。相反,这些处理在4 h时显着减少了总的细胞迁移和差异细胞迁移,而对Cg胸膜炎的晚期(48 h)几乎没有影响。这些发现扩展了以前的结果,并证明促炎性细胞因子TNF-α和IL-1beta在控制由小鼠胸膜腔注射Cg引起的细胞迁移和渗出中具有关键作用。总之,这些发现可能与对气道炎症反应所涉及的机制的理解有关。版权所有2001,学术出版社。

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