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部分肝切除和对乙酰氨基酚诱导的急性肝衰竭后肝脏再生的比较:基于转录组分析的全球图片。

Comparison of liver regeneration after partial hepatectomy and acetaminophen-induced acute liver failure: A global picture based on transcriptome analysis.

机构信息

Department of Pathology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

Department of Molecular and Integrative Physiology, Kansas City, KS, USA.

出版信息

Food Chem Toxicol. 2020 May;139:111186. doi: 10.1016/j.fct.2020.111186. Epub 2020 Feb 8.

DOI:10.1016/j.fct.2020.111186
PMID:32045647
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7687355/
Abstract

Liver regenerates following surgical removal and after drug-induced liver injury (DILI). However, most of the mechanisms of liver regeneration were identified using partial hepatectomy (PHX) model rather than using DILI models. We compared mechanisms of liver regeneration following PHX and after acetaminophen (APAP) overdose, a DILI model, using transcriptomic approach. Kinetics of hepatocyte proliferation and global gene expression profiles were studied in male C57BL/6J mice either subjected to PHX or following APAP overdose. Liver regeneration was much more synchronized after PHX as compared to APAP overdose. Transcriptomics analysis revealed activation of common upstream regulators in both models including growth factors HGF, EGF and VEGF; and cytokines IL6 and TNFα. However, magnitude of activation and temporality was significantly differed between the two models. HGF and VEGF showed similar activation between PHX and APAP but activation of EGF was significantly stronger in the APAP model. Activation of IL6 and TNFα transcriptional programs was delayed but remarkably higher in APAP. These dissimilarities could be attributed to inherent differences in the two models including significant injury and inflammation exclusively in the APAP model. This study highlights need to study mechanisms of liver regeneration after DILI separately from the mechanisms of regeneration PHX.

摘要

肝脏在手术切除和药物性肝损伤 (DILI) 后会再生。然而,大多数肝脏再生机制是使用部分肝切除术 (PHX) 模型而不是 DILI 模型来确定的。我们使用转录组学方法比较了 PHX 后和乙酰氨基酚 (APAP) 过量后(DILI 模型)肝脏再生的机制。在雄性 C57BL/6J 小鼠中,研究了 PHX 或 APAP 过量后肝细胞增殖的动力学和全局基因表达谱。与 APAP 过量相比,PHX 后的肝脏再生更加同步。转录组学分析显示,两种模型中常见的上游调节因子(包括生长因子 HGF、EGF 和 VEGF;细胞因子 IL6 和 TNFα)均被激活。然而,两种模型之间的激活幅度和时间性有很大差异。PHX 和 APAP 之间 HGF 和 VEGF 的激活相似,但 APAP 模型中 EGF 的激活明显更强。IL6 和 TNFα 转录程序的激活延迟,但在 APAP 中显著升高。这些差异可能归因于两种模型之间的固有差异,包括 APAP 模型中仅有的显著损伤和炎症。这项研究强调需要分别研究 DILI 后肝脏再生的机制和 PHX 的再生机制。

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本文引用的文献

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Liver Regeneration after Acetaminophen Hepatotoxicity: Mechanisms and Therapeutic Opportunities.对乙酰氨基酚肝毒性后的肝脏再生:机制与治疗机会。
Am J Pathol. 2019 Apr;189(4):719-729. doi: 10.1016/j.ajpath.2018.12.006. Epub 2019 Jan 14.
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TGFβ inhibition restores a regenerative response in acute liver injury by suppressing paracrine senescence.TGFβ 抑制通过抑制旁分泌衰老恢复急性肝损伤的再生反应。
Sci Transl Med. 2018 Aug 15;10(454). doi: 10.1126/scitranslmed.aan1230.
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Combined Systemic Disruption of MET and Epidermal Growth Factor Receptor Signaling Causes Liver Failure in Normal Mice.联合系统破坏 MET 和表皮生长因子受体信号导致正常小鼠肝衰竭。
Am J Pathol. 2018 Oct;188(10):2223-2235. doi: 10.1016/j.ajpath.2018.06.009. Epub 2018 Jul 20.
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