• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Deletion of the Mitochondrial Protein VWA8 Induces Oxidative Stress and an HNF4α Compensatory Response in Hepatocytes.线粒体蛋白 VWA8 的缺失诱导肝细胞氧化应激和 HNF4α 补偿反应。
Biochemistry. 2019 Dec 10;58(49):4983-4996. doi: 10.1021/acs.biochem.9b00863. Epub 2019 Nov 20.
2
Deletion of Von Willebrand A Domain Containing Protein (VWA8) raises activity of mitochondrial electron transport chain complexes in hepatocytes.含血管性血友病因子A结构域蛋白(VWA8)的缺失提高了肝细胞中线粒体电子传递链复合物的活性。
Biochem Biophys Rep. 2021 Feb 15;26:100928. doi: 10.1016/j.bbrep.2021.100928. eCollection 2021 Jul.
3
Characterization of the novel protein KIAA0564 (Von Willebrand Domain-containing Protein 8).新型蛋白质KIAA0564(含血管性血友病因子结构域蛋白8)的特性分析。
Biochem Biophys Res Commun. 2017 Jun 3;487(3):545-551. doi: 10.1016/j.bbrc.2017.04.067. Epub 2017 Apr 13.
4
Von Willebrand factor A domain-containing protein 8 (VWA8) localizes to the matrix side of the inner mitochondrial membrane.血管性血友病因子 A 结构域蛋白 8(VWA8)定位于线粒体内膜的基质侧。
Biochem Biophys Res Commun. 2020 Jan 1;521(1):158-163. doi: 10.1016/j.bbrc.2019.10.095. Epub 2019 Oct 17.
5
High fat diet-induced oxidative stress blocks hepatocyte nuclear factor 4α and leads to hepatic steatosis in mice.高脂饮食诱导的氧化应激会阻断肝细胞核因子 4α,导致小鼠肝脂肪变性。
J Cell Physiol. 2018 Jun;233(6):4770-4782. doi: 10.1002/jcp.26270. Epub 2018 Jan 15.
6
The spatial and developmental expression of mouse Vwa8 (von Willebrand domain-containing protein 8).小鼠Vwa8(含血管性血友病因子结构域蛋白8)的空间表达及发育表达
Gene Expr Patterns. 2018 Sep;29:39-46. doi: 10.1016/j.gep.2018.04.004. Epub 2018 Apr 13.
7
Hepatocyte nuclear factor 4alpha is implicated in endoplasmic reticulum stress-induced acute phase response by regulating expression of cyclic adenosine monophosphate responsive element binding protein H.肝细胞核因子4α通过调节环磷酸腺苷反应元件结合蛋白H的表达参与内质网应激诱导的急性期反应。
Hepatology. 2008 Oct;48(4):1242-50. doi: 10.1002/hep.22439.
8
Pharmacological inhibition of NOX4 ameliorates alcohol-induced liver injury in mice through improving oxidative stress and mitochondrial function.药理学抑制 NOX4 可通过改善氧化应激和线粒体功能来减轻小鼠的酒精性肝损伤。
Biochim Biophys Acta Gen Subj. 2017 Jan;1861(1 Pt A):2912-2921. doi: 10.1016/j.bbagen.2016.09.009. Epub 2016 Sep 12.
9
Cyp1b1 affects external control of mouse hepatocytes, fatty acid homeostasis and signaling involving HNF4α and PPARα.细胞色素P450 1B1(Cyp1b1)影响小鼠肝细胞的外部调控、脂肪酸稳态以及涉及肝细胞核因子4α(HNF4α)和过氧化物酶体增殖物激活受体α(PPARα)的信号传导。
Arch Biochem Biophys. 2016 May 1;597:30-47. doi: 10.1016/j.abb.2016.03.030. Epub 2016 Mar 29.
10
Protein arginine methyl transferase 1- and Jumonji C domain-containing protein 6-dependent arginine methylation regulate hepatocyte nuclear factor 4 alpha expression and hepatocyte proliferation in mice.蛋白精氨酸甲基转移酶 1 和含 Jumonji C 结构域蛋白 6 依赖性精氨酸甲基化调控小鼠肝细胞核因子 4α表达和肝细胞增殖。
Hepatology. 2018 Mar;67(3):1109-1126. doi: 10.1002/hep.29587. Epub 2018 Jan 24.

引用本文的文献

1
Modelling Peroxisomal Disorders in Zebrafish.斑马鱼中过氧化物酶体疾病的建模
Cells. 2025 Jan 20;14(2):147. doi: 10.3390/cells14020147.
2
Exploring the Role of Glycine Metabolism in Coronary Artery Disease: Insights from Human Genetics and Mouse Models.探索甘氨酸代谢在冠状动脉疾病中的作用:来自人类遗传学和小鼠模型的见解。
Nutrients. 2025 Jan 6;17(1):198. doi: 10.3390/nu17010198.
3
Translation Fidelity and Respiration Deficits in CLPP-Deficient Tissues: Mechanistic Insights from Mitochondrial Complexome Profiling.CLPP 缺陷组织中的翻译保真度和呼吸缺陷:线粒体复合物组学分析的机制见解。
Int J Mol Sci. 2023 Dec 15;24(24):17503. doi: 10.3390/ijms242417503.
4
Hepatic nuclear factor 4 alpha promotes the ferroptosis of lung adenocarcinoma transcriptional activation of cytochrome P450 oxidoreductase.肝核因子 4α促进肺腺癌的铁死亡:细胞色素 P450 氧化还原酶的转录激活。
PeerJ. 2023 May 8;11:e15377. doi: 10.7717/peerj.15377. eCollection 2023.
5
Mutated Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish.突变与发育迟缓、小头畸形和脊柱侧弯相关,并在斑马鱼的早期发育和骨骼形态发生中发挥新作用。
Front Cell Dev Biol. 2021 Oct 1;9:736960. doi: 10.3389/fcell.2021.736960. eCollection 2021.
6
Deletion of Von Willebrand A Domain Containing Protein (VWA8) raises activity of mitochondrial electron transport chain complexes in hepatocytes.含血管性血友病因子A结构域蛋白(VWA8)的缺失提高了肝细胞中线粒体电子传递链复合物的活性。
Biochem Biophys Rep. 2021 Feb 15;26:100928. doi: 10.1016/j.bbrep.2021.100928. eCollection 2021 Jul.
7
Metabolomic and transcriptomic profiling reveals the alteration of energy metabolism in oyster larvae during initial shell formation and under experimental ocean acidification.代谢组学和转录组学分析揭示了牡蛎幼虫在初始壳形成过程中和在实验海洋酸化下能量代谢的变化。
Sci Rep. 2020 Apr 9;10(1):6111. doi: 10.1038/s41598-020-62963-3.

本文引用的文献

1
High Fat Diet-Induced Changes in Hepatic Protein Abundance in Mice.高脂饮食诱导的小鼠肝脏蛋白质丰度变化
J Proteomics Bioinform. 2012;5(3):60-66. doi: 10.4172/jpb.1000214. Epub 2012 Feb 29.
2
Mitochondrial and cytosolic sources of hydrogen peroxide in resting C2C12 myoblasts.静止 C2C12 成肌细胞中线粒体和细胞质来源的过氧化氢。
Free Radic Biol Med. 2019 Jan;130:140-150. doi: 10.1016/j.freeradbiomed.2018.10.448. Epub 2018 Oct 31.
3
The Oxidative Stress Response Requires the NHR-49 Transcription Factor.氧化应激反应需要NHR-49转录因子。
G3 (Bethesda). 2018 Dec 10;8(12):3857-3863. doi: 10.1534/g3.118.200727.
4
NHR-49/HNF4 integrates regulation of fatty acid metabolism with a protective transcriptional response to oxidative stress and fasting.NHR-49/HNF4 整合了脂肪酸代谢的调节与对氧化应激和禁食的保护性转录反应。
Aging Cell. 2018 Jun;17(3):e12743. doi: 10.1111/acel.12743. Epub 2018 Mar 5.
5
Protective effect of genetic deletion of pannexin1 in experimental mouse models of acute and chronic liver disease.缝隙连接蛋白 1 基因缺失对急性和慢性肝病实验小鼠模型的保护作用。
Biochim Biophys Acta Mol Basis Dis. 2018 Mar;1864(3):819-830. doi: 10.1016/j.bbadis.2017.12.013. Epub 2017 Dec 12.
6
Hepatocyte-specific deletion of BAP31 promotes SREBP1C activation, promotes hepatic lipid accumulation, and worsens IR in mice.肝细胞特异性敲除 BAP31 可促进 SREBP1C 激活,促进肝脏脂质堆积,并加重小鼠的 IR。
J Lipid Res. 2018 Jan;59(1):35-47. doi: 10.1194/jlr.M077016. Epub 2017 Nov 7.
7
Activation of the STING-IRF3 pathway promotes hepatocyte inflammation, apoptosis and induces metabolic disorders in nonalcoholic fatty liver disease.STING-IRF3 通路的激活可促进肝细胞炎症、凋亡,并诱导非酒精性脂肪性肝病的代谢紊乱。
Metabolism. 2018 Apr;81:13-24. doi: 10.1016/j.metabol.2017.09.010. Epub 2017 Oct 26.
8
Proteomic Analyses of Cysteine Redox in High-Fat-Fed and Fasted Mouse Livers: Implications for Liver Metabolic Homeostasis.高脂肪喂养和饥饿状态下小鼠肝脏半胱氨酸氧化还原的蛋白质组学分析:对肝脏代谢稳态的影响。
J Proteome Res. 2018 Jan 5;17(1):129-140. doi: 10.1021/acs.jproteome.7b00431. Epub 2017 Nov 10.
9
NOX4 functions as a mitochondrial energetic sensor coupling cancer metabolic reprogramming to drug resistance.NOX4作为一种线粒体能量传感器,将癌症代谢重编程与耐药性联系起来。
Nat Commun. 2017 Oct 19;8(1):997. doi: 10.1038/s41467-017-01106-1.
10
Point mutation of Ffar1 abrogates fatty acid-dependent insulin secretion, but protects against HFD-induced glucose intolerance.FFAR1 点突变可消除脂肪酸依赖性胰岛素分泌,但可预防 HFD 诱导的葡萄糖不耐受。
Mol Metab. 2017 Oct;6(10):1304-1312. doi: 10.1016/j.molmet.2017.07.007. Epub 2017 Jul 18.

线粒体蛋白 VWA8 的缺失诱导肝细胞氧化应激和 HNF4α 补偿反应。

Deletion of the Mitochondrial Protein VWA8 Induces Oxidative Stress and an HNF4α Compensatory Response in Hepatocytes.

机构信息

Division of Endocrinology, Department of Medicine , University of Arizona College of Medicine , Tucson , Arizona 85724 , United States.

Mayo Clinic in Arizona , Scottsdale , Arizona 85259 , United States.

出版信息

Biochemistry. 2019 Dec 10;58(49):4983-4996. doi: 10.1021/acs.biochem.9b00863. Epub 2019 Nov 20.

DOI:10.1021/acs.biochem.9b00863
PMID:31702900
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8925280/
Abstract

von Willebrand A domain-containing protein 8 (VWA8) is a poorly characterized, mitochondrial matrix-targeted protein with an AAA ATPase domain and ATPase activity that increases in livers of mice fed a high-fat diet. This study was undertaken to use CRISPR/Cas9 to delete VWA8 in cultured mouse hepatocytes and gain insight into its function. Unbiased omics techniques and bioinformatics were used to guide subsequent assays, including the assessment of oxidative stress and the determination of bioenergetic capacity. Metabolomics analysis showed VWA8 null cells had higher levels of oxidative stress and protein degradation; assays of hydrogen peroxide production revealed higher levels of production of reactive oxygen species (ROS). Proteomics and transcriptomics analyses showed VWA8 null cells had higher levels of expression of mitochondrial proteins (electron transport-chain Complex I, ATP synthase), peroxisomal proteins, and lipid transport proteins. The pattern of higher protein abundance in the VWA8 null cells could be explained by a higher level of hepatocyte nuclear factor 4 α (HNF4α) expression. Bioenergetic assays showed higher rates of carbohydrate oxidation and mitochondrial and nonmitochondrial lipid oxidation in intact and permeabilized cells. Inhibitor assays localized sites of ROS production to peroxisomes and NOX1/4. The rescue of VWA8 protein restored the wild-type phenotype, and treatment with antioxidants decreased the level of HNF4α expression. Thus, loss of VWA8 produces a mitochondrial defect that may be sensed by NOX4, leading to an increase in the level of ROS that results in a higher level of HNF4α. The compensatory HNF4α response results in a higher oxidative capacity and an even higher level of ROS production. We hypothesize that VWA8 is an AAA ATPase protein that plays a role in mitochondrial protein quality.

摘要

血管性血友病因子 A 结构域蛋白 8(VWA8)是一种功能尚未完全阐明的线粒体基质靶向蛋白,具有 AAA ATP 酶结构域和 ATP 酶活性,在高脂饮食喂养的小鼠肝脏中其活性增加。本研究旨在使用 CRISPR/Cas9 技术在培养的小鼠肝细胞中敲除 VWA8,以深入了解其功能。采用无偏的组学技术和生物信息学方法来指导后续的检测,包括氧化应激评估和生物能量学能力测定。代谢组学分析显示,VWA8 缺失细胞的氧化应激和蛋白质降解水平更高;过氧化氢生成检测显示,活性氧(ROS)的产生水平更高。蛋白质组学和转录组学分析显示,VWA8 缺失细胞中线粒体蛋白(电子传递链复合物 I、ATP 合酶)、过氧化物酶体蛋白和脂质转运蛋白的表达水平更高。VWA8 缺失细胞中更高水平的蛋白质丰度模式可以通过更高水平的肝细胞核因子 4α(HNF4α)表达来解释。生物能量学检测显示,完整和通透细胞中糖氧化、线粒体和非线粒体脂质氧化的速率更高。抑制剂检测将 ROS 产生的部位定位于过氧化物酶体和 NOX1/4。VWA8 蛋白的恢复挽救了野生型表型,抗氧化剂处理降低了 HNF4α 的表达水平。因此,VWA8 的缺失会导致线粒体缺陷,这可能被 NOX4 感知,导致 ROS 水平升高,从而导致 HNF4α 水平升高。代偿性的 HNF4α 反应导致更高的氧化能力和更高水平的 ROS 产生。我们假设 VWA8 是一种 AAA ATP 酶蛋白,在维持线粒体蛋白质质量方面发挥作用。