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Possible Involvement of Liver Resident Macrophages (Kupffer Cells) in the Pathogenesis of Both Intrahepatic and Extrahepatic Inflammation

机译:肝脏常见血栓药中可能参与(Kupffer细胞)在肝内和脱毛症的发病机制中

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Liver resident macrophages designated Kupffer cells (KCs) form the largest subpopulation of tissue macrophages. KCs are involved in the pathogenesis of liver inflammation. However, the role of KCs in the systemic inflammation is still elusive. In this study, we examined whether KCs are involved in not only intrahepatic inflammation but also extrahepatic systemic inflammation. Administration of clodronate liposomes resulted in the KC deletion and in the suppression of liver injury in T cell-mediated hepatitis by ConA as a local acute inflammation model, while the treatment did not influence dextran sulfate sodium- (DSS-) induced colitis featured by weight loss, intestinal shrink, and pathological observation as an ectopic local acute inflammation model. In contrast, KC deletion inhibited collagen-induced arthritis as a model of extrahepatic, systemic chronical inflammation. KC deleted mice showed weaker arthritic scores, less joint swelling, and more joint space compared to arthritis-induced control mice. These results strongly suggest that KCs are involved in not only intrahepatic inflammatory response but also systemic (especially) chronic inflammation.
机译:肝脏常规巨噬细胞指定Kupffer细胞(KCS)形成组织巨噬细胞的最大亚群。 KCS参与肝脏炎症的发病机制。然而,KCS在全身炎症中的作用仍然难以捉摸。在这项研究中,我们检查了KCS是否涉及肝内炎症,还涉及肝内炎症。施用克莱膦酸盐脂质体导致KC缺失和抑制T细胞介导的肝炎的肝损伤,CONA作为局部急性炎症模型,而治疗不影响重量的葡聚糖硫酸钠 - (DSS-)诱导的结肠炎损失,肠收缩和病理观察作为异位局部急性急性炎症模型。相比之下,KC缺失抑制胶原蛋白诱导的关节炎作为脱毛,全身慢性炎症的模型。与关节炎诱导的对照小鼠相比,KC缺失的小鼠表现出较弱的关节炎评分,较少的关节肿胀和更多的关节空间。这些结果强烈表明KC不仅涉及肝内炎症反应,而且涉及系统性(特别是)慢性炎症。

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