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1
The Mer receptor tyrosine kinase is expressed on discrete macrophage subpopulations and mainly uses Gas6 as its ligand for uptake of apoptotic cells.Mer受体酪氨酸激酶在离散的巨噬细胞亚群上表达,主要利用生长停滞特异性蛋白6(Gas6)作为其摄取凋亡细胞的配体。
Clin Immunol. 2009 Oct;133(1):138-44. doi: 10.1016/j.clim.2009.06.002. Epub 2009 Jul 24.
2
Diversification of TAM receptor tyrosine kinase function.TAM 受体酪氨酸激酶功能的多样化。
Nat Immunol. 2014 Oct;15(10):920-8. doi: 10.1038/ni.2986. Epub 2014 Sep 7.
3
Impaired apoptotic cell clearance in the germinal center by Mer-deficient tingible body macrophages leads to enhanced antibody-forming cell and germinal center responses.Mer 缺陷的易染体巨噬细胞清除生发中心凋亡细胞的能力受损,导致抗体形成细胞和生发中心反应增强。
J Immunol. 2010 Nov 15;185(10):5859-68. doi: 10.4049/jimmunol.1001187. Epub 2010 Oct 15.
4
A soluble form of the Mer receptor tyrosine kinase inhibits macrophage clearance of apoptotic cells and platelet aggregation.Mer受体酪氨酸激酶的可溶性形式可抑制巨噬细胞对凋亡细胞的清除以及血小板聚集。
Blood. 2007 Feb 1;109(3):1026-33. doi: 10.1182/blood-2006-05-021634. Epub 2006 Oct 17.
5
Axl and MerTK receptor tyrosine kinases maintain human macrophage efferocytic capacity in the presence of viral triggers.Axl 和 MerTK 受体酪氨酸激酶在病毒触发存在的情况下维持人类巨噬细胞的吞噬能力。
Eur J Immunol. 2018 May;48(5):855-860. doi: 10.1002/eji.201747283. Epub 2018 Feb 22.
6
Apoptotic cells promote their own clearance and immune tolerance through activation of the nuclear receptor LXR.凋亡细胞通过激活核受体LXR促进自身清除和免疫耐受。
Immunity. 2009 Aug 21;31(2):245-58. doi: 10.1016/j.immuni.2009.06.018. Epub 2009 Jul 30.
7
A role for Mer tyrosine kinase in alphavbeta5 integrin-mediated phagocytosis of apoptotic cells.Mer酪氨酸激酶在αvβ5整合素介导的凋亡细胞吞噬作用中的作用。
J Cell Sci. 2005 Feb 1;118(Pt 3):539-53. doi: 10.1242/jcs.01632.
8
RhoA/phosphatidylinositol 3-kinase/protein kinase B/mitogen-activated protein kinase signaling after growth arrest-specific protein 6/mer receptor tyrosine kinase engagement promotes epithelial cell growth and wound repair via upregulation of hepatocyte growth factor in macrophages.生长停滞特异性蛋白6/mer受体酪氨酸激酶结合后,RhoA/磷脂酰肌醇3激酶/蛋白激酶B/丝裂原活化蛋白激酶信号传导通过上调巨噬细胞中的肝细胞生长因子来促进上皮细胞生长和伤口修复。
J Pharmacol Exp Ther. 2014 Sep;350(3):563-77. doi: 10.1124/jpet.114.215673. Epub 2014 Jun 17.
9
Regulation of microglial phagocytosis and inflammatory gene expression by Gas6 acting on the Axl/Mer family of tyrosine kinases.Gas6通过作用于酪氨酸激酶的Axl/Mer家族来调节小胶质细胞的吞噬作用和炎症基因表达。
J Neuroimmune Pharmacol. 2008 Jun;3(2):130-40. doi: 10.1007/s11481-007-9090-2. Epub 2007 Oct 10.
10
Macrophages and dendritic cells use different Axl/Mertk/Tyro3 receptors in clearance of apoptotic cells.巨噬细胞和树突状细胞在清除凋亡细胞过程中使用不同的Axl/Mertk/Tyro3受体。
J Immunol. 2007 May 1;178(9):5635-42. doi: 10.4049/jimmunol.178.9.5635.

引用本文的文献

1
Heterogeneity of Neutrophils and Immunological Function in Neonatal Sepsis: Analysis of Molecular Subtypes Based on Hypoxia-Glycolysis-Lactylation.新生儿脓毒症中中性粒细胞的异质性及免疫功能:基于缺氧-糖酵解-乳酸化的分子亚型分析
Mediators Inflamm. 2025 Mar 26;2025:5790261. doi: 10.1155/mi/5790261. eCollection 2025.
2
Differential regulation of lung homeostasis and silicosis by the TAM receptors MerTk and Axl.TAM 受体 MerTk 和 Axl 对肺稳态和矽肺的差异化调节。
Front Immunol. 2024 May 7;15:1380628. doi: 10.3389/fimmu.2024.1380628. eCollection 2024.
3
Axl and MerTK regulate synovial inflammation and are modulated by IL-6 inhibition in rheumatoid arthritis.AXL 和 MerTK 调节滑膜炎症,并可被类风湿关节炎中的 IL-6 抑制所调节。
Nat Commun. 2024 Mar 16;15(1):2398. doi: 10.1038/s41467-024-46564-6.
4
Apoptotic cell fragments locally activate tingible body macrophages in the germinal center.凋亡细胞碎片在生发中心局部激活含铁血黄素小体巨噬细胞。
Cell. 2023 Mar 16;186(6):1144-1161.e18. doi: 10.1016/j.cell.2023.02.004. Epub 2023 Mar 2.
5
Alcohol and HIV-Derived Hepatocyte Apoptotic Bodies Induce Hepatic Stellate Cell Activation.酒精和HIV衍生的肝细胞凋亡小体可诱导肝星状细胞活化。
Biology (Basel). 2022 Jul 14;11(7):1059. doi: 10.3390/biology11071059.
6
Construction of the axolotl cell landscape using combinatorial hybridization sequencing at single-cell resolution.利用单细胞分辨率组合杂交测序构建蝾螈细胞图谱。
Nat Commun. 2022 Jul 22;13(1):4228. doi: 10.1038/s41467-022-31879-z.
7
The Akt-mTORC1 pathway mediates Axl receptor tyrosine kinase-induced mesangial cell proliferation.Akt-mTORC1 通路介导 Axl 受体酪氨酸激酶诱导的系膜细胞增殖。
J Leukoc Biol. 2022 Mar;111(3):563-571. doi: 10.1002/JLB.2A1220-850RRR. Epub 2021 Jul 4.
8
Immuno-oncology: are TAM receptors in glioblastoma friends or foes?免疫肿瘤学:胶质母细胞瘤中的 TAM 受体是敌是友?
Cell Commun Signal. 2021 Jan 28;19(1):11. doi: 10.1186/s12964-020-00694-8.
9
The TAM family as a therapeutic target in combination with radiation therapy.TAM家族作为与放射治疗联合使用的治疗靶点。
Emerg Top Life Sci. 2017 Dec;1(5):493-500. doi: 10.1042/etls20170066. Epub 2017 Dec 12.
10
MERTK is a host factor that promotes classical swine fever virus entry and antagonizes innate immune response in PK-15 cells.MERTK 是一种宿主因子,可促进猪瘟病毒进入细胞,并在 PK-15 细胞中拮抗先天免疫反应。
Emerg Microbes Infect. 2020 Mar 14;9(1):571-581. doi: 10.1080/22221751.2020.1738278. eCollection 2020.

本文引用的文献

1
A defect in Marco expression contributes to systemic lupus erythematosus development via failure to clear apoptotic cells.Marco表达缺陷通过未能清除凋亡细胞而导致系统性红斑狼疮的发展。
J Immunol. 2009 Feb 15;182(4):1982-90. doi: 10.4049/jimmunol.0801320.
2
TAM receptor tyrosine kinases: biologic functions, signaling, and potential therapeutic targeting in human cancer.TAM受体酪氨酸激酶:生物学功能、信号传导及在人类癌症中的潜在治疗靶点
Adv Cancer Res. 2008;100:35-83. doi: 10.1016/S0065-230X(08)00002-X.
3
Immunobiology of the TAM receptors.TAM 受体的免疫生物学
Nat Rev Immunol. 2008 May;8(5):327-36. doi: 10.1038/nri2303.
4
Auto-oxidation and oligomerization of protein S on the apoptotic cell surface is required for Mer tyrosine kinase-mediated phagocytosis of apoptotic cells.凋亡细胞表面蛋白S的自氧化和寡聚化是Mer酪氨酸激酶介导的凋亡细胞吞噬作用所必需的。
J Immunol. 2008 Feb 15;180(4):2522-30. doi: 10.4049/jimmunol.180.4.2522.
5
MerTK is required for apoptotic cell-induced T cell tolerance.凋亡细胞诱导的T细胞耐受性需要MerTK。
J Exp Med. 2008 Jan 21;205(1):219-32. doi: 10.1084/jem.20062293. Epub 2008 Jan 14.
6
Macrophages and dendritic cells use different Axl/Mertk/Tyro3 receptors in clearance of apoptotic cells.巨噬细胞和树突状细胞在清除凋亡细胞过程中使用不同的Axl/Mertk/Tyro3受体。
J Immunol. 2007 May 1;178(9):5635-42. doi: 10.4049/jimmunol.178.9.5635.
7
Structural basis for Gas6-Axl signalling.Gas6-Axl信号传导的结构基础。
EMBO J. 2006 Jan 11;25(1):80-7. doi: 10.1038/sj.emboj.7600912. Epub 2005 Dec 15.
8
Regulation of blood coagulation by the protein C anticoagulant pathway: novel insights into structure-function relationships and molecular recognition.蛋白C抗凝途径对血液凝固的调节:结构-功能关系及分子识别的新见解
Arterioscler Thromb Vasc Biol. 2005 Jul;25(7):1311-20. doi: 10.1161/01.ATV.0000168421.13467.82. Epub 2005 Apr 28.
9
Macrophage receptors and immune recognition.巨噬细胞受体与免疫识别。
Annu Rev Immunol. 2005;23:901-44. doi: 10.1146/annurev.immunol.23.021704.115816.
10
A novel site contributing to growth-arrest-specific gene 6 binding to its receptors as revealed by a human monoclonal antibody.一种由人单克隆抗体揭示的、有助于生长停滞特异性基因6与其受体结合的新位点。
Biochem J. 2005 May 1;387(Pt 3):727-35. doi: 10.1042/BJ20040859.

Mer受体酪氨酸激酶在离散的巨噬细胞亚群上表达,主要利用生长停滞特异性蛋白6(Gas6)作为其摄取凋亡细胞的配体。

The Mer receptor tyrosine kinase is expressed on discrete macrophage subpopulations and mainly uses Gas6 as its ligand for uptake of apoptotic cells.

作者信息

Shao Wen-Hai, Zhen Yuxuan, Eisenberg Robert A, Cohen Philip L

机构信息

Department of Medicine, Division of Rheumatology, Temple University, Philadelphia, PA 19140, USA.

出版信息

Clin Immunol. 2009 Oct;133(1):138-44. doi: 10.1016/j.clim.2009.06.002. Epub 2009 Jul 24.

DOI:10.1016/j.clim.2009.06.002
PMID:19631584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2746995/
Abstract

The Mer receptor tyrosine kinase is both an important mediator of apoptotic cell phagocytosis and a regulator of macrophage and DC cytokine production. Since phenotypically distinguishable macrophages are known to have different functions, we have examined Mer expression of murine splenic macrophages. We also used serum deficient in the Mer ligand, growth arrest-specific protein 6 (Gas6) to define better the role of this Mer ligand in macrophage function. By immunofluorescence staining, we found Mer to be strongly expressed in splenic red pulp, largely on platelets. We also found Mer expression on marginal zone macrophages. Strikingly, all tingible body macrophages bore Mer. In functional phagocytosis assays of apoptotic cells, Gas6 appeared to be the sole ligand for Mer, and this system accounted for about 30% of splenic macrophage phagocytosis of apoptotic cells. Taken together, the expression pattern of Mer on macrophage subpopulations in the spleen and its Gas6-dependent role in macrophage phagocytosis suggest an important role for Mer in the modulation of immune responses.

摘要

Mer受体酪氨酸激酶既是凋亡细胞吞噬作用的重要介质,也是巨噬细胞和树突状细胞细胞因子产生的调节因子。由于已知表型可区分的巨噬细胞具有不同功能,我们检测了小鼠脾脏巨噬细胞的Mer表达。我们还使用缺乏Mer配体生长停滞特异性蛋白6(Gas6)的血清,以更好地确定这种Mer配体在巨噬细胞功能中的作用。通过免疫荧光染色,我们发现Mer在脾脏红髓中大量表达,主要位于血小板上。我们还在边缘区巨噬细胞上发现了Mer表达。令人惊讶的是,所有可染小体巨噬细胞都带有Mer。在凋亡细胞的功能性吞噬试验中,Gas6似乎是Mer的唯一配体,并且该系统约占脾脏巨噬细胞对凋亡细胞吞噬作用的30%。综上所述,Mer在脾脏巨噬细胞亚群上的表达模式及其在巨噬细胞吞噬作用中依赖Gas6的作用表明Mer在免疫反应调节中具有重要作用。