• 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

一份细胞类型解析的肝脏蛋白质组

A Cell-type-resolved Liver Proteome.

作者信息

Ding Chen, Li Yanyan, Guo Feifei, Jiang Ying, Ying Wantao, Li Dong, Yang Dong, Xia Xia, Liu Wanlin, Zhao Yan, He Yangzhige, Li Xianyu, Sun Wei, Liu Qiongming, Song Lei, Zhen Bei, Zhang Pumin, Qian Xiaohong, Qin Jun, He Fuchu

机构信息

From the ‡State Key Laboratory of Proteomics, Beijing Proteome Research Center, Beijing Institute of Radiation Medicine, Beijing 100039, China; §National Center for Protein Sciences (The PHOENIX center, Beijing), Beijing 102206, China; **State Key Laboratory of Genetic Engineering and Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Institute of Biomedical Sciences, Fudan University, Shanghai 200433, China.

¶School of Life Sciences, Tsinghua University, Beijing 100084, China.

出版信息

Mol Cell Proteomics. 2016 Oct;15(10):3190-3202. doi: 10.1074/mcp.M116.060145. Epub 2016 Aug 25.

DOI:10.1074/mcp.M116.060145
PMID:27562671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5054343/
Abstract

Parenchymatous organs consist of multiple cell types, primarily defined as parenchymal cells (PCs) and nonparenchymal cells (NPCs). The cellular characteristics of these organs are not well understood. Proteomic studies facilitate the resolution of the molecular details of different cell types in organs. These studies have significantly extended our knowledge about organogenesis and organ cellular composition. Here, we present an atlas of the cell-type-resolved liver proteome. In-depth proteomics identified 6000 to 8000 gene products (GPs) for each cell type and a total of 10,075 GPs for four cell types. This data set revealed features of the cellular composition of the liver: (1) hepatocytes (PCs) express the least GPs, have a unique but highly homogenous proteome pattern, and execute fundamental liver functions; (2) the division of labor among PCs and NPCs follows a model in which PCs make the main components of pathways, but NPCs trigger the pathways; and (3) crosstalk among NPCs and PCs maintains the PC phenotype. This study presents the liver proteome at cell resolution, serving as a research model for dissecting the cell type constitution and organ features at the molecular level.

摘要

实质器官由多种细胞类型组成,主要分为实质细胞(PCs)和非实质细胞(NPCs)。这些器官的细胞特征尚未得到充分了解。蛋白质组学研究有助于解析器官中不同细胞类型的分子细节。这些研究极大地扩展了我们对器官发生和器官细胞组成的认识。在此,我们展示了一份细胞类型解析的肝脏蛋白质组图谱。深入的蛋白质组学研究为每种细胞类型鉴定出6000至8000个基因产物(GPs),四种细胞类型总共鉴定出10,075个GPs。该数据集揭示了肝脏细胞组成的特征:(1)肝细胞(PCs)表达的GPs最少,具有独特但高度同质的蛋白质组模式,并执行肝脏的基本功能;(2)PCs和NPCs之间的分工遵循一种模式,即PCs构成通路的主要成分,但NPCs触发这些通路;(3)NPCs和PCs之间的相互作用维持了PCs的表型。本研究以细胞分辨率展示了肝脏蛋白质组,为在分子水平剖析细胞类型构成和器官特征提供了一个研究模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c79f/5054343/7a9e6fbf0b71/zjw0101654310004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c79f/5054343/23db52d3f285/zjw0101654310001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c79f/5054343/91f8822bce52/zjw0101654310002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c79f/5054343/4a8301f225e9/zjw0101654310003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c79f/5054343/7a9e6fbf0b71/zjw0101654310004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c79f/5054343/23db52d3f285/zjw0101654310001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c79f/5054343/91f8822bce52/zjw0101654310002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c79f/5054343/4a8301f225e9/zjw0101654310003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c79f/5054343/7a9e6fbf0b71/zjw0101654310004.jpg

相似文献

1
A Cell-type-resolved Liver Proteome.一份细胞类型解析的肝脏蛋白质组
Mol Cell Proteomics. 2016 Oct;15(10):3190-3202. doi: 10.1074/mcp.M116.060145. Epub 2016 Aug 25.
2
Spatial Proteomics of Single Hepatocytes with Multiplexed Data-Independent Acquisition (mDIA).单细胞的空间蛋白质组学与多重数据非依赖采集(mDIA)。
Methods Mol Biol. 2024;2817:97-113. doi: 10.1007/978-1-0716-3934-4_9.
3
A Cytological Atlas of the Human Liver Proteome from PROTEOME-LIVER 2.0, a Publicly Available Database.人类肝脏蛋白质组的细胞学图集来自 PROTEOME-LIVER 2.0,这是一个公开可用的数据库。
J Proteome Res. 2022 Aug 5;21(8):1916-1929. doi: 10.1021/acs.jproteome.2c00190. Epub 2022 Jul 12.
4
Cell-type-resolved quantitative proteomics of murine liver.鼠肝细胞类型分辨定量蛋白质组学。
Cell Metab. 2014 Dec 2;20(6):1076-87. doi: 10.1016/j.cmet.2014.11.002.
5
Global protein expression profiling of zebrafish organs based on in vivo incorporation of stable isotopes.基于稳定同位素的体内掺入对斑马鱼器官进行全球蛋白质表达谱分析。
J Proteome Res. 2014 Apr 4;13(4):2162-74. doi: 10.1021/pr5000335. Epub 2014 Mar 21.
6
Adult hepatocytes direct liver organogenesis through non-parenchymal cell recruitment in the kidney.成体肝细胞通过招募肾中非实质细胞来指导肝发生。
J Hepatol. 2018 Apr;68(4):744-753. doi: 10.1016/j.jhep.2017.12.016. Epub 2017 Dec 26.
7
Cooperation of liver cells in health and disease.健康与疾病状态下肝细胞的协作。
Adv Anat Embryol Cell Biol. 2001;161:III-XIII, 1-151. doi: 10.1007/978-3-642-56553-3.
8
Cell-type-resolved proteomic analysis of the human liver.人类肝脏的细胞类型解析蛋白质组学分析
Liver Int. 2020 Jul;40(7):1770-1780. doi: 10.1111/liv.14452. Epub 2020 Apr 12.
9
Differential protein expression of blood platelet components associated with adverse transfusion reactions.与不良反应输血反应相关的血小板成分的差异蛋白质表达。
J Proteomics. 2019 Mar 1;194:25-36. doi: 10.1016/j.jprot.2018.12.019. Epub 2018 Dec 24.
10
Proteome analysis of hepatic non-parenchymal cells of immune liver fibrosis rats.免疫性肝纤维化大鼠肝非实质细胞的蛋白质组分析
Sci China Life Sci. 2014 Mar;57(3):303-314. doi: 10.1007/s11427-014-4619-0. Epub 2014 Feb 21.

引用本文的文献

1
Deficiency of Ugcg in LSECs alleviates high-fat diet-induced MASLD.肝窦内皮细胞中Ugcg的缺乏可缓解高脂饮食诱导的代谢相关脂肪性肝病。
Hepatol Commun. 2025 Sep 5;9(9). doi: 10.1097/HC9.0000000000000793. eCollection 2025 Sep 1.
2
The coming era of proteomics-driven precision medicine.蛋白质组学驱动的精准医学时代即将来临。
Natl Sci Rev. 2025 Jul 14;12(8):nwaf278. doi: 10.1093/nsr/nwaf278. eCollection 2025 Aug.
3
Gasdermin D aggravates a mouse model of radiation-induced liver disease by promoting chemokine secretion and neutrophil recruitment.

本文引用的文献

1
Transcriptome analysis of individual stromal cell populations identifies stroma-tumor crosstalk in mouse lung cancer model.对单个基质细胞群体的转录组分析确定了小鼠肺癌模型中的基质-肿瘤相互作用。
Cell Rep. 2015 Feb 24;10(7):1187-201. doi: 10.1016/j.celrep.2015.01.040. Epub 2015 Feb 19.
2
Proteomics. Tissue-based map of the human proteome.蛋白质组学。人类蛋白质组组织图谱。
Science. 2015 Jan 23;347(6220):1260419. doi: 10.1126/science.1260419.
3
Cell-type-resolved quantitative proteomics of murine liver.鼠肝细胞类型分辨定量蛋白质组学。
Gasdermin D通过促进趋化因子分泌和中性粒细胞募集加重辐射诱导的肝病小鼠模型。
Nat Commun. 2025 Jul 2;16(1):6064. doi: 10.1038/s41467-025-61397-7.
4
Spatial patterns of hepatocyte glucose flux revealed by stable isotope tracing and multi-scale microscopy.通过稳定同位素示踪和多尺度显微镜揭示的肝细胞葡萄糖通量的空间模式。
Nat Commun. 2025 Jul 1;16(1):5850. doi: 10.1038/s41467-025-60994-w.
5
Deciphering Age-Dependent ECM Remodelling in Liver: Proteomic Profiling and Its Implications for Aging and Therapeutic Targets.解析肝脏中年龄依赖性细胞外基质重塑:蛋白质组学分析及其对衰老和治疗靶点的影响
Cell Prolif. 2025 Sep;58(9):e70087. doi: 10.1111/cpr.70087. Epub 2025 Jun 19.
6
The EGFR Pathway as a Potential Therapeutic Target for Modulation of Radiation-induced Liver Injury.表皮生长因子受体(EGFR)信号通路作为调节放射性肝损伤的潜在治疗靶点
Radiat Res. 2025 May 1;203(5):293-303. doi: 10.1667/RADE-24-00203.1.
7
Turnover atlas of proteome and phosphoproteome across mouse tissues and brain regions.小鼠组织和脑区蛋白质组及磷酸化蛋白质组的周转图谱。
Cell. 2025 Apr 17;188(8):2267-2287.e21. doi: 10.1016/j.cell.2025.02.021. Epub 2025 Mar 20.
8
Region- and Cell-type-Resolved Multiomic Atlas of the Heart.心脏的区域和细胞类型解析多组学图谱
Mol Cell Proteomics. 2025 May;24(5):100922. doi: 10.1016/j.mcpro.2025.100922. Epub 2025 Feb 5.
9
An Extensive Atlas of Proteome and Phosphoproteome Turnover Across Mouse Tissues and Brain Regions.小鼠组织和脑区蛋白质组及磷酸化蛋白质组周转的综合图谱
bioRxiv. 2024 Oct 17:2024.10.15.618303. doi: 10.1101/2024.10.15.618303.
10
Branched-chain amino acid metabolism: Pathophysiological mechanism and therapeutic intervention in metabolic diseases.支链氨基酸代谢:代谢性疾病的病理生理机制及治疗干预
Obes Rev. 2025 Feb;26(2):e13856. doi: 10.1111/obr.13856. Epub 2024 Oct 25.
Cell Metab. 2014 Dec 2;20(6):1076-87. doi: 10.1016/j.cmet.2014.11.002.
4
CellNet: network biology applied to stem cell engineering.细胞网络:应用于干细胞工程的网络生物学
Cell. 2014 Aug 14;158(4):903-915. doi: 10.1016/j.cell.2014.07.020.
5
Hepatic inflammation and fibrosis: functional links and key pathways.肝脏炎症与纤维化:功能联系及关键通路
Hepatology. 2015 Mar;61(3):1066-79. doi: 10.1002/hep.27332. Epub 2015 Jan 28.
6
Visual account of protein investment in cellular functions.蛋白质在细胞功能中的投资的直观描述。
Proc Natl Acad Sci U S A. 2014 Jun 10;111(23):8488-93. doi: 10.1073/pnas.1314810111. Epub 2014 Jun 2.
7
Mass-spectrometry-based draft of the human proteome.基于质谱的人类蛋白质组草图。
Nature. 2014 May 29;509(7502):582-7. doi: 10.1038/nature13319.
8
A draft map of the human proteome.人类蛋白质组草图。
Nature. 2014 May 29;509(7502):575-81. doi: 10.1038/nature13302.
9
SILAC proteomics of planarians identifies Ncoa5 as a conserved component of pluripotent stem cells.秀丽隐杆线虫 SILAC 蛋白质组学鉴定 Ncoa5 为多能干细胞的保守成分。
Cell Rep. 2013 Nov 27;5(4):1142-55. doi: 10.1016/j.celrep.2013.10.035. Epub 2013 Nov 21.
10
The IUPHAR/BPS Guide to PHARMACOLOGY: an expert-driven knowledgebase of drug targets and their ligands.国际药理学联合会/英国药理学学会药物靶点和配体百科全书:一个由专家驱动的药物靶点和配体知识库。
Nucleic Acids Res. 2014 Jan;42(Database issue):D1098-106. doi: 10.1093/nar/gkt1143. Epub 2013 Nov 14.