Suppr超能文献

肝脏脂质蓄积导致 Tenascin-C 过表达加重非酒精性脂肪性肝病小鼠肝缺血/再灌注损伤。

Overproduction of Tenascin-C Driven by Lipid Accumulation in the Liver Aggravates Hepatic Ischemia/Reperfusion Injury in Steatotic Mice.

机构信息

The Dumont-UCLA Transplant Center, Division of Liver and Pancreas Transplantation, Department of Surgery, David Geffen School of Medicine at UCLA, University of California, Los Angeles, Los Angeles, CA.

出版信息

Liver Transpl. 2019 Feb;25(2):288-301. doi: 10.1002/lt.25365.

Abstract

The purpose of this study was to assess the significance of tenascin-C (Tnc) expression in steatotic liver ischemia/reperfusion injury (IRI). The critical shortage in donor organs has led to the use of steatotic livers in transplantation regardless of their elevated susceptibility to hepatic IRI. Tnc is an endogenous danger signal extracellular matrix molecule involved in various aspects of immunity and tissue injury. In the current study, mice were fed with a steatosis-inducing diet and developed approximately 50% hepatic steatosis, predominantly macrovesicular, before being subjected to hepatic IRI. We report here that lipid accumulation in hepatocytes inflated the production of Tnc in steatotic livers and in isolated hepatic stellate cells. Moreover, we show that the inability of Tnc-/- deficient steatotic mice to express Tnc significantly protected these mice from liver IRI. Compared with fatty controls, Tnc-/- steatotic mice showed significantly reduced serum transaminase levels and enhanced liver histological preservation at both 6 and 24 hours after hepatic IRI. The lack of Tnc expression resulted in impaired lymphocyte antigen 6 complex, locus (Ly6G) neutrophil and macrophage antigen-1 (Mac-1) leukocyte recruitment as well as in decreased expression of proinflammatory mediators (interleukin 1β, tumor necrosis factor α, and chemokine [C-X-C motif] ligand 2) after liver reperfusion. Myeloperoxidase (MPO) is the most abundant cytotoxic enzyme secreted by neutrophils and a key mediator of neutrophil-induced oxidative tissue injuries. Using an in vitro model of steatosis, we also show that Tnc markedly potentiated the effect of steatotic hepatocytes on neutrophil-derived MPO activity. In conclusion, our data support the view that inhibition of Tnc is a promising therapeutic approach to lessen inflammation in steatotic livers and to maximize their successful use in organ transplantation.

摘要

本研究旨在评估 tenascin-C(Tnc)在脂肪肝缺血/再灌注损伤(IRI)中的表达意义。由于供体器官严重短缺,即使脂肪肝对肝 IRI 的易感性增加,也将其用于移植。Tnc 是一种内源性危险信号细胞外基质分子,参与免疫和组织损伤的各个方面。在本研究中,我们用致脂肪肝饮食喂养小鼠,使约 50%的肝脏发生脂肪变性,主要为大泡性脂肪变性,然后进行肝 IRI。我们在此报告,肝细胞内脂质堆积会增加脂肪肝中 Tnc 的产生,也会增加分离的肝星状细胞中 Tnc 的产生。此外,我们表明,缺乏 Tnc 的脂肪肝小鼠无法表达 Tnc,这显著保护了这些小鼠免受肝 IRI 的影响。与肥胖对照组相比,Tnc-/-脂肪肝小鼠在肝 IRI 后 6 小时和 24 小时时,血清转氨酶水平显著降低,肝组织保存得到改善。缺乏 Tnc 表达导致淋巴细胞抗原 6 复合物、座(Ly6G)中性粒细胞和巨噬细胞抗原-1(Mac-1)白细胞募集受损,以及再灌注后促炎介质(白细胞介素 1β、肿瘤坏死因子 α 和趋化因子 [C-X-C 基序] 配体 2)表达减少。髓过氧化物酶(MPO)是中性粒细胞分泌的最丰富的细胞毒性酶,也是中性粒细胞诱导的氧化组织损伤的关键介质。我们还使用脂肪肝体外模型表明,Tnc 明显增强了脂肪肝肝细胞对中性粒细胞衍生的 MPO 活性的影响。总之,我们的数据支持这样一种观点,即抑制 Tnc 是减轻脂肪肝炎症和最大限度地成功将其用于器官移植的一种有前途的治疗方法。

相似文献

本文引用的文献

1
Innate immune responses to trauma.创伤的先天免疫反应。
Nat Immunol. 2018 Apr;19(4):327-341. doi: 10.1038/s41590-018-0064-8. Epub 2018 Mar 5.
5
Neutrophils: a cornerstone of liver ischemia and reperfusion injury.中性粒细胞:肝缺血再灌注损伤的基石。
Lab Invest. 2018 Jan;98(1):51-62. doi: 10.1038/labinvest.2017.90. Epub 2017 Sep 18.
7
Myeloperoxidase: A new player in autoimmunity.髓过氧化物酶:自身免疫中的新角色。
Cell Immunol. 2017 Jul;317:1-8. doi: 10.1016/j.cellimm.2017.05.002. Epub 2017 May 10.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验