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Monocyte chemoattractant protein-1 is not required for liver regeneration after partial hepatectomy

机译:部分肝切除术后肝再生不需要单核细胞化学蛋白-1

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Background Liver regeneration following 70?% partial hepatectomy (PH) requires the coordinated expression of soluble mediators produced by macrophages. Monocyte chemoattractant protein-1 (MCP-1) is a potent stimulus of monocyte recruitment and macrophage activation. The goal of this study was to determine how MCP-1 contributes to liver regeneration. Methods PH was performed on anesthetized C57Bl/6 (wild type) and MCP-1 knockout mice, and macrophage-produced cytokines and hepatocyte proliferation were measured. Results In wild type mice, hepatic MCP-1 protein levels increased 4–6?h after PH, and elevated plasma MCP-1 levels were detected 12?h after PH. Hepatocyte proliferation was comparable in MCP-1 knockout and wild type mice, as was the expression of macrophage-derived cytokines, TNFα and IL-6, and levels of phosphorylated STAT3. The number of CCR2sup+/sup cells in the liver was similar in MCP-1 knockout and wild type mice, which suggests that other chemokines may recruit CCR2sup+/sup cells in the absence of MCP-1. Studies with CCR2 knockout mice revealed that hepatocyte proliferation was suppressed ~40?% compared to wild type mice 36?h after PH, but proliferation and liver-body-weight ratios were similar at 48?h. Conclusion These findings suggest that MCP-1 is not required for PH-induced liver regeneration, yet the role of CCR2 warrants further study.
机译:背景技术肝再生后70℃的部分肝切除术(pH)需要通过巨噬细胞产生的可溶性介质的协调表达。单核细胞化学蛋白-1(MCP-1)是单核细胞募集和巨噬细胞活化的有效刺激。本研究的目标是确定MCP-1如何为肝再生有助于促进肝脏再生。方法对麻醉的C57BL / 6(野生型)和MCP-1敲除小鼠进行pH,并测量巨噬细胞产生的细胞因子和肝细胞增殖。结果野生型小鼠,在pH后,肝脏MCP-1蛋白水平增加4-6〜6℃,并在pH后检测升高的血浆MCP-1水平。肝细胞增殖在MCP-1敲除和野生型小鼠中是相当的,如巨噬细胞衍生的细胞因子,TNFα和IL-6的表达,以及磷酸化STAT3的水平。肝脏中CCR2 + / sup>细胞的数量在MCP-1敲除和野生型小鼠中相似,这表明其他趋化因子可以在没有MCP的情况下募集CCR2 + 细胞-1。用CCR2敲除小鼠的研究表明,与pH后的野生型小鼠36〜H相比,肝细胞增殖抑制〜40≤%,但增殖和肝体重比在48℃下相似。结论这些研究结果表明,PH诱导的肝再生不需要MCP-1,但CCR2认证的作用进一步研究。

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