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Effects of lipopolysaccharide and dexamethasone on the biological characteristics of rats alveolar macrophage

机译:脂多糖和地塞米松对大鼠肺泡巨噬细胞生物学特性的影响

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Alveolar macrophages(AMs) play a central role in lung inflammation and acute lung injury, but also participate actively in the resolution of inflammation after activation. Macrophages (Mφ) represent a dynamic cell population that develops and operates within a changing microenvironment. However, it is not known how the biological characteristic of AM stimulates by lipopolysaccharide (LPS) or desamethasone (DEX) and the relationship between AM and inflammation. In this study, we first observed the morphology in AM isolated from rats differed according to the molecule used. We found that LPS-stimulated AM induced anti-apoptosis and had pro-inflammatory effects; dexamethasone induced AM apoptosis and had anti-inflammatory effects. These results suggested that a balance in macrophage activation, being either stimulated by LPS) or DEX, would be important to participate sequentially in both the induction and the resolution of inflammation. These findings may provide new insight into the lung inflammatory process as well as new fields of investigation for immunotherapy in the fields of acute lung injury/ acute respiratory distress syndrome.
机译:肺泡巨噬细胞(AMS)在肺炎和急性肺损伤中起着核心作用,但也在激活后积极参与炎症。巨噬细胞(Mφ)表示动态小区群,在改变的微环境中开发和操作。然而,它不知道如何通过脂多糖(LPS)或地塞米松(DEX)AM刺激了的生物学特性和AM和炎症之间的关系。在这项研究中,我们首先观察到am中am中am的形态根据所用的分子不同。我们发现LPS刺激的AM诱导抗细胞凋亡并具有促炎作用;地塞米松诱导患有细胞凋亡并具有抗炎作用。这些结果表明,由LPS刺激的巨噬细胞激活中的平衡是重要的,在诱导和炎症的分辨率中依次参与。这些发现可能会对肺炎的新洞察力提供新的洞察力,以及急性肺损伤/急性呼吸窘迫综合征领域的免疫疗法调查新领域。

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