• 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
Genetic Models of Macrophage Depletion.巨噬细胞耗竭的遗传模型。
Methods Mol Biol. 2018;1784:243-258. doi: 10.1007/978-1-4939-7837-3_22.
2
Functional significance of mononuclear phagocyte populations generated through adult hematopoiesis.成年造血过程中产生的单核吞噬细胞群体的功能意义。
J Leukoc Biol. 2014 Dec;96(6):969-80. doi: 10.1189/jlb.1RI0414-195R. Epub 2014 Sep 15.
3
CSF1R-dependent macrophages control postnatal somatic growth and organ maturation.CSF1R 依赖性巨噬细胞控制出生后躯体生长和器官成熟。
PLoS Genet. 2021 Jun 3;17(6):e1009605. doi: 10.1371/journal.pgen.1009605. eCollection 2021 Jun.
4
Self-renewing macrophages--a new line of enquiries in mononuclear phagocytes.自我更新的巨噬细胞——单核吞噬细胞研究的新方向
Immunobiology. 2015 Feb;220(2):169-74. doi: 10.1016/j.imbio.2014.11.005. Epub 2014 Nov 11.
5
Could a B-1 cell derived phagocyte "be one" of the peritoneal macrophages during LPS-driven inflammation?在 LPS 驱动的炎症反应中,B-1 细胞衍生的吞噬细胞“能成为”腹腔巨噬细胞之一吗?
PLoS One. 2012;7(3):e34570. doi: 10.1371/journal.pone.0034570. Epub 2012 Mar 30.
6
Role of colony stimulating factor-1 in the establishment and regulation of tissue macrophages during postnatal development of the mouse.集落刺激因子-1在小鼠出生后发育过程中组织巨噬细胞的建立和调节中的作用。
Development. 1994 Jun;120(6):1357-72. doi: 10.1242/dev.120.6.1357.
7
Tissue-resident macrophages self-maintain locally throughout adult life with minimal contribution from circulating monocytes.组织驻留巨噬细胞在整个成年期在局部自我维持,来自循环单核细胞的贡献很小。
Immunity. 2013 Apr 18;38(4):792-804. doi: 10.1016/j.immuni.2013.04.004.
8
The Phagocytic Function of Macrophage-Enforcing Innate Immunity and Tissue Homeostasis.巨噬细胞的吞噬功能——先天免疫与组织动态平衡的执行者。
Int J Mol Sci. 2017 Dec 29;19(1):92. doi: 10.3390/ijms19010092.
9
From proliferation to proliferation: monocyte lineage comes full circle.从增殖到增殖:单核细胞谱系循环往复。
Semin Immunopathol. 2014 Mar;36(2):137-48. doi: 10.1007/s00281-013-0409-1. Epub 2014 Jan 17.
10
In vivo depletion and genetic targeting of mouse intestinal CX3CR1(+) mononuclear phagocytes.小鼠肠道CX3CR1(+)单核吞噬细胞的体内清除与基因靶向
J Immunol Methods. 2016 May;432:13-23. doi: 10.1016/j.jim.2015.12.009. Epub 2015 Dec 17.

引用本文的文献

1
CD4 skin resident memory T cells preferentially colocalize with dermal Folr2 macrophages in contact hypersensitivity.在接触性超敏反应中,CD4皮肤驻留记忆T细胞优先与真皮层Folr2巨噬细胞共定位。
Front Immunol. 2025 Jul 28;16:1590687. doi: 10.3389/fimmu.2025.1590687. eCollection 2025.
2
Bioengineered liver crosslinked with nano-graphene oxide enables efficient liver regeneration via MMP suppression and immunomodulation.生物工程化肝脏与纳米氧化石墨烯交联,通过抑制 MMP 和免疫调节实现高效肝脏再生。
Nat Commun. 2023 Feb 13;14(1):801. doi: 10.1038/s41467-023-35941-2.
3
Transient depletion of macrophages alters local inflammatory response at the site of disc herniation in a transgenic mouse model.在转基因小鼠模型中,巨噬细胞的短暂耗竭会改变椎间盘突出部位的局部炎症反应。
Osteoarthritis Cartilage. 2023 Jul;31(7):894-907. doi: 10.1016/j.joca.2023.01.574. Epub 2023 Feb 7.
4
The Gut-Liver Axis in Chronic Liver Disease: A Macrophage Perspective.慢性肝病中的肠-肝轴:巨噬细胞的视角。
Cells. 2021 Oct 30;10(11):2959. doi: 10.3390/cells10112959.
5
The Role of Macrophages During Zebrafish Injury and Tissue Regeneration Under Infectious and Non-Infectious Conditions.巨噬细胞在斑马鱼感染和非感染性损伤及组织再生过程中的作用。
Front Immunol. 2021 Jul 21;12:707824. doi: 10.3389/fimmu.2021.707824. eCollection 2021.
6
Cross-Talk Between Inflammation and Fibroblast Growth Factor 10 During Organogenesis and Pathogenesis: Lessons Learnt From the Lung and Other Organs.器官发生和发病机制过程中炎症与成纤维细胞生长因子10之间的相互作用:从肺和其他器官中获得的经验教训
Front Cell Dev Biol. 2021 May 31;9:656883. doi: 10.3389/fcell.2021.656883. eCollection 2021.
7
Liposomal Clodronate-mediated Macrophage Depletion in the Zebrafish Model.脂质体氯膦酸盐介导的斑马鱼模型巨噬细胞清除
Bio Protoc. 2021 Mar 20;11(6):e3951. doi: 10.21769/BioProtoc.3951.
8
Function of Macrophages in Disease: Current Understanding on Molecular Mechanisms.巨噬细胞在疾病中的功能:分子机制的现有理解。
Front Immunol. 2021 Mar 8;12:620510. doi: 10.3389/fimmu.2021.620510. eCollection 2021.
9
Systemic dendrimer delivery of triptolide to tumor-associated macrophages improves anti-tumor efficacy and reduces systemic toxicity in glioblastoma.树状大分子系统递呈雷公藤红素至肿瘤相关巨噬细胞可改善胶质母细胞瘤的抗肿瘤疗效并降低全身毒性。
J Control Release. 2021 Jan 10;329:434-444. doi: 10.1016/j.jconrel.2020.12.003. Epub 2020 Dec 5.
10
Determining macrophage versus neutrophil contributions to innate immunity using larval zebrafish.利用斑马鱼幼鱼确定巨噬细胞与中性粒细胞对先天免疫的贡献。
Dis Model Mech. 2020 Jan 9;13(1):dmm041889. doi: 10.1242/dmm.041889.

本文引用的文献

1
Macrophage biology and immunology: man is not a mouse.巨噬细胞生物学与免疫学:人类并非小鼠。
J Leukoc Biol. 2007 Mar;81(3):579. doi: 10.1189/jlb.1106702.
2
M1 Means Kill; M2 Means Heal.M1代表杀戮;M2代表治愈。
J Immunol. 2017 Oct 1;199(7):2191-2193. doi: 10.4049/jimmunol.1701135.
3
CD206 M2-like macrophages regulate systemic glucose metabolism by inhibiting proliferation of adipocyte progenitors.CD206 M2 样巨噬细胞通过抑制脂肪细胞祖细胞的增殖来调节全身葡萄糖代谢。
Nat Commun. 2017 Aug 18;8(1):286. doi: 10.1038/s41467-017-00231-1.
4
Macrophages Facilitate Electrical Conduction in the Heart.巨噬细胞促进心脏中的电传导。
Cell. 2017 Apr 20;169(3):510-522.e20. doi: 10.1016/j.cell.2017.03.050.
5
Regulation of Inflammation- and Infection-Driven Hematopoiesis.炎症和感染驱动的造血调控。
Trends Immunol. 2017 May;38(5):345-357. doi: 10.1016/j.it.2017.01.004. Epub 2017 Feb 16.
6
Inflammatory macrophages can transdifferentiate into myofibroblasts during renal fibrosis.在肾纤维化过程中,炎性巨噬细胞可转分化为肌成纤维细胞。
Cell Death Dis. 2016 Dec 1;7(12):e2495. doi: 10.1038/cddis.2016.402.
7
Tissue-specific contribution of macrophages to wound healing.组织特异性巨噬细胞在伤口愈合中的作用。
Semin Cell Dev Biol. 2017 Jan;61:3-11. doi: 10.1016/j.semcdb.2016.08.006. Epub 2016 Aug 10.
8
Macrophage A2A Adenosine Receptors Are Essential to Protect from Progressive Kidney Injury.巨噬细胞A2A腺苷受体对于预防进行性肾损伤至关重要。
Am J Pathol. 2016 Oct;186(10):2601-13. doi: 10.1016/j.ajpath.2016.06.017. Epub 2016 Aug 9.
9
Macrophage Infiltration and Alternative Activation during Wound Healing Promote MEK1-Induced Skin Carcinogenesis.伤口愈合过程中的巨噬细胞浸润和替代性激活促进MEK1诱导的皮肤癌发生。
Cancer Res. 2016 Feb 15;76(4):805-817. doi: 10.1158/0008-5472.CAN-14-3676. Epub 2016 Jan 11.
10
Alveolar Macrophages Are a Prominent but Nonessential Target for Murine Cytomegalovirus Infecting the Lungs.肺泡巨噬细胞是小鼠巨细胞病毒感染肺部时的主要但非必需靶标。
J Virol. 2015 Dec 30;90(6):2756-66. doi: 10.1128/JVI.02856-15.

巨噬细胞耗竭的遗传模型。

Genetic Models of Macrophage Depletion.

作者信息

Hua Li, Shi Jiayuan, Shultz Leonard D, Ren Guangwen

机构信息

The Jackson Laboratory, Bar Harbor, ME, USA.

出版信息

Methods Mol Biol. 2018;1784:243-258. doi: 10.1007/978-1-4939-7837-3_22.

DOI:10.1007/978-1-4939-7837-3_22
PMID:29761404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6333569/
Abstract

Macrophages are a heterogeneous population of innate immune cells and are distributed in most adult tissues. Certain tissue-resident macrophages with a prenatal origin, together with postnatal monocyte-derived macrophages, serve as the host scavenger system to eliminate invading pathogens, malignant cells, senescent cells, dead cells, cellular debris, and other foreign substances. As a key member of the mononuclear phagocyte system, macrophages play essential roles in regulation of prenatal development, tissue homeostasis, and disease progression. Over the past two decades, considerable efforts have been made to generate genetic models of macrophage ablation in mice. These models support investigations of the precise functions of tissue-specific macrophages under physiological and pathological conditions. Herein, we overview the currently available mouse strains for in vivo genetic ablation of macrophages and discuss their respective advantages and limitations.

摘要

巨噬细胞是先天性免疫细胞的异质性群体,分布于大多数成年组织中。某些起源于产前的组织驻留巨噬细胞,与产后单核细胞衍生的巨噬细胞一起,作为宿主清除系统,以清除入侵的病原体、恶性细胞、衰老细胞、死亡细胞、细胞碎片和其他外来物质。作为单核吞噬细胞系统的关键成员,巨噬细胞在产前发育、组织稳态和疾病进展的调节中发挥着重要作用。在过去二十年中,人们为建立小鼠巨噬细胞消融的遗传模型付出了巨大努力。这些模型有助于研究生理和病理条件下组织特异性巨噬细胞的精确功能。在此,我们概述了目前可用于体内巨噬细胞基因消融的小鼠品系,并讨论了它们各自的优缺点。