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干细胞因子及其受体c-kit,对于野生型和肿瘤坏死因子受体-1基因敲除小鼠在70%肝切除术后的肝细胞增殖很重要。

Stem cell factor and its receptor, c-kit, are important for hepatocyte proliferation in wild-type and tumor necrosis factor receptor-1 knockout mice after 70% hepatectomy.

作者信息

Ren Xiaodan, Hu Bin, Colletti Lisa

机构信息

Department of Surgery, University of Michigan Medical School, Ann Arbor, Mich.

出版信息

Surgery. 2008 Jun;143(6):790-802. doi: 10.1016/j.surg.2008.03.021.

Abstract

BACKGROUND

Stem cell factor (SCF) has well-known proliferative effects on hematopoietic cells. SCF also has effects on differentiation and proliferation in other cell types. Interleukin-6 (IL-6) and tumor necrosis factor (TNF)-alpha have proliferative effects in the liver. Recent studies in our laboratory have linked SCF's hepatoproliferative actions to those of IL-6, demonstrating that IL-6-induced hepatocyte proliferation depends, at least in part, on SCF. We now hypothesize that TNF-alpha's hepatoproliferative effects are also dependent on SCF.

METHODS AND RESULTS

In vitro studies using primary mouse hepatocytes show that SCF is induced by TNF-alpha; anti-SCF antibody treatment in this system inhibits TNF-alpha-induced hepatocyte proliferation, suggesting that TNF-alpha-induced hepatocyte proliferation is also SCF dependent. Additional in vivo experiments were performed in which wild type and/or TNF-alpha receptor-1 knockout mice (TNFR1(-/-)) were subjected to 70% hepatectomy or sham laparotomy. TNFR1(-/-) mice are known to have delayed hepatic regeneration after partial hepatectomy. Initial experiments demonstrated that the SCF receptor, c-kit, is upregulated after partial hepatectomy in wild-type mice, further emphasizing the importance of this system in the restoration of hepatic mass. SCF administration to TNFR1(-/-) mice in the context of partial hepatectomy restores hepatocyte proliferation to normal. Further, SCF administration to TNFR1(-/-) mice before hepatectomy increases phosphotyrosine signal transducer and activator (p-stat-3) levels, suggesting that SCF-induced increases in hepatocyte proliferation may also be stat-3 mediated.

CONCLUSIONS

These data suggest that TNF-alpha-induced hepatocyte proliferation depends, at least in part, on SCF and that SCF and its receptor, c-kit, are important for the liver's regenerative processes.

摘要

背景

干细胞因子(SCF)对造血细胞具有众所周知的增殖作用。SCF对其他细胞类型的分化和增殖也有影响。白细胞介素-6(IL-6)和肿瘤坏死因子(TNF)-α在肝脏中具有增殖作用。我们实验室最近的研究将SCF的肝增殖作用与IL-6的作用联系起来,表明IL-6诱导的肝细胞增殖至少部分依赖于SCF。我们现在推测TNF-α的肝增殖作用也依赖于SCF。

方法和结果

使用原代小鼠肝细胞的体外研究表明,TNF-α可诱导SCF;在该系统中用抗SCF抗体处理可抑制TNF-α诱导的肝细胞增殖,提示TNF-α诱导的肝细胞增殖也依赖于SCF。进行了额外的体内实验,其中野生型和/或TNF-α受体-1基因敲除小鼠(TNFR1(-/-))接受70%肝切除术或假手术剖腹术。已知TNFR1(-/-)小鼠在部分肝切除术后肝再生延迟。初步实验表明,野生型小鼠部分肝切除术后SCF受体c-kit上调,进一步强调了该系统在肝脏质量恢复中的重要性。在部分肝切除的情况下给TNFR1(-/-)小鼠施用SCF可使肝细胞增殖恢复正常。此外,在肝切除术前给TNFR1(-/-)小鼠施用SCF可增加磷酸酪氨酸信号转导子和激活子(p-stat-3)水平,提示SCF诱导的肝细胞增殖增加也可能由stat-3介导。

结论

这些数据表明,TNF-α诱导的肝细胞增殖至少部分依赖于SCF,并且SCF及其受体c-kit对肝脏的再生过程很重要。

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Front Genet. 2021 Feb 2;12:598855. doi: 10.3389/fgene.2021.598855. eCollection 2021.
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IL-22 is involved in liver regeneration after hepatectomy.白细胞介素-22 参与肝切除术后的肝脏再生。
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