部分肝切除术后小鼠肝脏再生过程中tnf驱动的炎症及其在肝脏生长调节中的作用。

Molecular biotherapy Pub Date : 1991-09-01
M Satoh, K Adachi, T Suda, M Yamazaki, D Mizuno
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引用次数: 0

摘要

为了确定tnf驱动的炎症在细胞生长和分化的自我调节中的作用,研究了部分肝切除术后小鼠肝脏再生中tnf驱动的炎症。在第3天,当有丝分裂反应达到峰值时,肝切除术引起了全身和肝脏TNF生成的启动状态。肝脏组织化学研究也显示炎症症状;肝切除术后6小时出现肝细胞坏死灶。肿瘤坏死因子本身在肝切除术后第1 ~ 2天肝细胞增殖前短暂自发分泌。地塞米松降低肝切除术后TNF分泌和肝细胞增殖。重组小鼠TNF刺激肝细胞体外增殖。这些发现表明,肝切除术诱导肝脏短期分泌TNF, TNF驱动的炎症在肝脏再生中起重要作用,至少部分是通过直接刺激肝细胞增殖。
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TNF-driven inflammation during mouse liver regeneration after partial hepatectomy and its role in growth regulation of liver.

To determine the role of TNF-driven inflammation in self-regulation of cell growth and differentiation, mouse liver regeneration after partial hepatectomy was examined for TNF-driven inflammation. Hepatectomy provoked priming state for TNF production in both whole body and liver on day 3 when the peak mitotic response occurred. Histochemical studies of liver also showed an inflammatory symptom; hepatocellular necrotic foci appeared by 6 hours after hepatectomy. TNF itself was secreted spontaneously in liver transiently on day 1 to 2 after hepatectomy just before the proliferation of hepatocytes. Dexamethasone reduced both TNF secretion and hepatocyte proliferation after hepatectomy. Recombinant murine TNF stimulated the in vitro proliferation of hepatocytes. These findings indicate that hepatectomy induces short-term secretion of TNF in liver and TNF-driven inflammation has an important role in liver regeneration, at least in part by the direct stimulation of hepatocyte proliferation.

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