• 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

转录调控巨噬细胞多样性和特化。

Transcriptional control of macrophage diversity and specialization.

机构信息

Department of Experimental Oncology, European Institute of Oncology, IFOM-IEO Campus, Via Adamello, Milan, Italy.

出版信息

Eur J Immunol. 2011 Sep;41(9):2486-90. doi: 10.1002/eji.201141706.

DOI:10.1002/eji.201141706
PMID:21952802
Abstract

The key driving force underlying cell identity is represented by the complex and dynamic interplay between cell-intrinsic, lineage-restricted developmental pathways on the one hand, and cell-extrinsic, tissue-specific microenvironmental signals on the other. In this context, macrophages are a paradigmatic cell population whose functional specialization in vivo reflects the impact of the local microenvironment on the intrinsic differentiation program, leading to a variety of specialized macrophage types in different tissues and conditions; however, how this is translated into a biological outcome is not appreciably understood. The kind of investigations described in this Viewpoint aim to explore the inner determinants of cell identity and functional diversification at a genomic level; mechanisms that permit plastic cell types, like macrophages, to adapt to different environments.

摘要

细胞特性的关键驱动因素体现在细胞内在的、谱系限制的发育途径与细胞外在的、组织特异性的微环境信号之间的复杂和动态相互作用上。在这种情况下,巨噬细胞是一个典型的细胞群体,其体内的功能特化反映了局部微环境对内在分化程序的影响,导致不同组织和条件下存在多种特化的巨噬细胞类型;然而,这种影响如何转化为生物学结果还不太清楚。本观点中描述的研究旨在从基因组水平上探索细胞特性和功能多样化的内在决定因素;这些机制使像巨噬细胞这样的可塑性细胞类型能够适应不同的环境。

相似文献

1
Transcriptional control of macrophage diversity and specialization.转录调控巨噬细胞多样性和特化。
Eur J Immunol. 2011 Sep;41(9):2486-90. doi: 10.1002/eji.201141706.
2
Epigenetic control of macrophage polarization.巨噬细胞极化的表观遗传调控。
Eur J Immunol. 2011 Sep;41(9):2490-3. doi: 10.1002/eji.201141792.
3
Transcriptional control of macrophage identity, self-renewal, and function.巨噬细胞特性、自我更新和功能的转录控制。
Adv Immunol. 2013;120:269-300. doi: 10.1016/B978-0-12-417028-5.00010-7.
4
Transcription control of early B cell differentiation.早期 B 细胞分化的转录调控。
Curr Opin Immunol. 2010 Apr;22(2):161-7. doi: 10.1016/j.coi.2010.01.010. Epub 2010 Feb 9.
5
Transcriptional regulation in B cell differentiation.B细胞分化中的转录调控。
Crit Rev Immunol. 1999;19(2):127-53.
6
Macrophages in cancer and infectious diseases: the 'good' and the 'bad'.癌症和传染病中的巨噬细胞:“好”与“坏”。
Immunotherapy. 2011 Oct;3(10):1185-202. doi: 10.2217/imt.11.116.
7
Molecular control of activation and priming in macrophages.巨噬细胞中激活与启动的分子调控
Nat Immunol. 2016 Jan;17(1):26-33. doi: 10.1038/ni.3306.
8
The interferon-inducible gene, Ifi204, is transcriptionally activated in response to M-CSF, and its expression favors macrophage differentiation in myeloid progenitor cells.干扰素诱导基因Ifi204在M-CSF的作用下被转录激活,其表达有利于髓系祖细胞向巨噬细胞分化。
J Leukoc Biol. 2006 Jan;79(1):173-83. doi: 10.1189/jlb.0205083. Epub 2005 Oct 21.
9
Distinct stage-specific cis-active transcriptional mechanisms control expression of T cell coreceptor CD8 alpha at double- and single-positive stages of thymic development.不同的阶段特异性顺式作用转录机制控制胸腺发育双阳性和单阳性阶段T细胞共受体CD8α的表达。
J Immunol. 1998 Sep 1;161(5):2254-66.
10
An intronic silencer regulates B lymphocyte cell- and stage-specific expression of the human complement receptor type 2 (CR2, CD21) gene.一个内含子沉默子调节人类补体受体2(CR2,CD21)基因在B淋巴细胞中的细胞及阶段特异性表达。
J Immunol. 1998 Feb 1;160(3):1268-78.

引用本文的文献

1
Development of nucleus-targeted histone-tail-based photoaffinity probes to profile the epigenetic interactome in native cells.用于分析天然细胞中表观遗传相互作用组的细胞核靶向组蛋白尾部光亲和探针的开发。
Nat Commun. 2025 Jan 6;16(1):415. doi: 10.1038/s41467-024-55046-8.
2
Flow Cytometric Characterization of Macrophages Infected with Serovar Typhimurium Expressing Red Fluorescent Protein.表达红色荧光蛋白的鼠伤寒血清型沙门氏菌感染巨噬细胞的流式细胞术表征
Bio Protoc. 2022 Jun 5;12(11):e4440. doi: 10.21769/BioProtoc.4440.
3
Two Faces of Macrophages: Training and Tolerance.
巨噬细胞的两面:训练与耐受
Biomedicines. 2021 Nov 2;9(11):1596. doi: 10.3390/biomedicines9111596.
4
Cytokine-Mediated Regulation of ARG1 in Macrophages and Its Impact on the Control of Serovar Typhimurium Infection.细胞因子介导的巨噬细胞中 ARG1 的调节及其对鼠伤寒沙门氏菌感染控制的影响。
Cells. 2021 Jul 19;10(7):1823. doi: 10.3390/cells10071823.
5
Diversity, Mechanisms, and Significance of Macrophage Plasticity.巨噬细胞可塑性的多样性、机制及意义。
Annu Rev Pathol. 2020 Jan 24;15:123-147. doi: 10.1146/annurev-pathmechdis-012418-012718. Epub 2019 Sep 17.
6
MicroRNAs as Molecular Switches in Macrophage Activation.MicroRNAs 作为巨噬细胞活化的分子开关。
Front Immunol. 2019 Apr 17;10:799. doi: 10.3389/fimmu.2019.00799. eCollection 2019.
7
Acquired immunological imbalance after surgery with cardiopulmonary bypass due to epigenetic over-activation of PU.1/M-CSF.心肺转流手术后获得性免疫失衡是由于 PU.1/M-CSF 的表观遗传过度激活。
J Transl Med. 2018 May 25;16(1):143. doi: 10.1186/s12967-018-1518-3.
8
Macrophage Ontogeny Underlies Differences in Tumor-Specific Education in Brain Malignancies.巨噬细胞个体发生是脑恶性肿瘤中肿瘤特异性驯化差异的基础。
Cell Rep. 2016 Nov 22;17(9):2445-2459. doi: 10.1016/j.celrep.2016.10.052. Epub 2016 Nov 10.
9
NLRC4 suppresses melanoma tumor progression independently of inflammasome activation.NLRC4独立于炎性小体激活抑制黑色素瘤肿瘤进展。
J Clin Invest. 2016 Oct 3;126(10):3917-3928. doi: 10.1172/JCI86953. Epub 2016 Sep 12.
10
Epigenetic Control of Macrophage Polarisation and Soluble Mediator Gene Expression during Inflammation.炎症过程中巨噬细胞极化和可溶性介质基因表达的表观遗传调控
Mediators Inflamm. 2016;2016:6591703. doi: 10.1155/2016/6591703. Epub 2016 Apr 10.