肝再生
糖蛋白130
再生(生物学)
肝细胞
细胞因子
白细胞介素
生物
细胞因子受体
细胞生物学
内分泌学
内科学
白细胞介素6
癌症研究
免疫学
医学
生物化学
体外
作者
Malte Peters,Guido Blinn,Thomas Jostock,Peter Schirmacher,Karl‐Hermann Meyer zum Büschenfelde,Peter R. Galle,Stefan Rose‐John
出处
期刊:Gastroenterology
[Elsevier BV]
日期:2000-12-01
卷期号:119 (6): 1663-1671
被引量:118
标识
DOI:10.1053/gast.2000.20236
摘要
Liver regeneration after loss of hepatic tissue leads to hepatocyte and nonparenchymal cell proliferation and rapid restoration of liver parenchyma. Interleukin (IL)-6 is a key inducer of transcription factors involved in liver regeneration. Whenever IL-6 activates target cells, it binds to a specific IL-6 receptor (IL-6R). The IL-6/IL-6R complex then associates with the signal transducer gp130, leading to activation of intracellular signaling.We have recently constructed the designer cytokine Hyper-IL-6 consisting of soluble IL-6R covalently linked to IL-6, which directly stimulates gp130 even in the absence of membrane-bound IL-6R. We compared the influence of IL-6 and Hyper-IL-6 on liver regeneration after partial hepatectomy in mice.The IL-6/soluble IL-6 fusion protein Hyper-IL-6, but not IL-6 alone, led to an earlier onset of hepatocellular proliferation resulting in an acceleration of liver weight restoration. Also, during liver regeneration, soluble IL-6R levels were increased.These results emphasize a central role for IL-6 and soluble IL-6R in liver regeneration and indicate a possible therapeutic potential for the designer cytokine Hyper-IL-6 in clinical situations associated with liver regeneration such as acute hepatic failure or resection of chronically damaged liver tissue.
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