Suppr超能文献

脂质环境调节巨噬细胞功能的变化。

Changes in macrophage function modulated by the lipid environment.

作者信息

Williams Michael R, Cauvi David M, Rivera Isabel, Hawisher Dennis, De Maio Antonio

机构信息

Initiative for Maximizing Student Development, University of California San Diego, La Jolla, CA, USA.

Department of Surgery, University of California San Diego, La Jolla, CA, USA.

出版信息

Innate Immun. 2016 Apr;22(3):141-51. doi: 10.1177/1753425916633886. Epub 2016 Mar 7.

Abstract

Macrophages (Mφs) play a critical role in the defense against pathogens, orchestrating the inflammatory response during injury and maintaining tissue homeostasis. During these processes, macrophages encounter a variety of environmental conditions that are likely to change their gene expression pattern, which modulates their function. In this study, we found that murine Mφs displayed two different subpopulations characterized by differences in morphologies, expression of surface markers and phagocytic capacity under non-stimulated conditions. These two subpopulations could be recapitulated by changes in the culture conditions. Thus, Mφs grown in suspension in the presence of serum were highly phagocytic, whereas subtraction of serum resulted in rapid attachment and reduced phagocytic activity. The difference in phagocytosis between these subpopulations was correlated with the expression levels of FcγR. These two cell subpopulations also differed in their responses to LPS and the expression of surface markers, including CD14, CD86, scavenger receptor A1, TLR4 and low-density lipoprotein receptor. Moreover, we found that the lipid/cholesterol content in the culture medium mediated the differences between these two cell subpopulations. Thus, we described a mechanism that modulates Mφ function depending on the exposure to lipids within their surrounding microenvironment.

摘要

巨噬细胞(Mφs)在抵御病原体、协调损伤期间的炎症反应以及维持组织稳态方面发挥着关键作用。在这些过程中,巨噬细胞会遇到各种可能改变其基因表达模式的环境条件,而基因表达模式的改变又会调节其功能。在本研究中,我们发现小鼠巨噬细胞在非刺激条件下表现出两种不同的亚群,其特征在于形态、表面标志物表达和吞噬能力的差异。这两种亚群可以通过培养条件的变化得以重现。因此,在血清存在下悬浮培养的巨噬细胞具有高度吞噬能力,而去除血清则导致细胞快速贴壁并降低吞噬活性。这些亚群之间吞噬作用的差异与FcγR的表达水平相关。这两种细胞亚群对脂多糖(LPS)的反应以及包括CD14、CD86、清道夫受体A1、Toll样受体4(TLR4)和低密度脂蛋白受体在内的表面标志物的表达也有所不同。此外,我们发现培养基中的脂质/胆固醇含量介导了这两种细胞亚群之间的差异。因此,我们描述了一种根据巨噬细胞周围微环境中脂质暴露情况来调节其功能的机制。

相似文献

1
Changes in macrophage function modulated by the lipid environment.
Innate Immun. 2016 Apr;22(3):141-51. doi: 10.1177/1753425916633886. Epub 2016 Mar 7.
4
CD36 Differently Regulates Macrophage Responses to Smooth and Rough Lipopolysaccharide.
PLoS One. 2016 Apr 13;11(4):e0153558. doi: 10.1371/journal.pone.0153558. eCollection 2016.
5
An interplay between scavenger receptor A and CD14 during activation of J774 cells by high concentrations of LPS.
Immunobiology. 2013 Oct;218(10):1217-26. doi: 10.1016/j.imbio.2013.04.005. Epub 2013 Apr 12.
7
Stable transduction of bovine TLR4 and bovine MD-2 into LPS-nonresponsive cells and soluble CD14 promote the ability to respond to LPS.
Vet Immunol Immunopathol. 2007 Jul 15;118(1-2):92-104. doi: 10.1016/j.vetimm.2007.04.017. Epub 2007 May 3.
8
TLR-mediated inflammatory response to neonatal pathogens and co-infection in neonatal immune cells.
Cytokine. 2014 Oct;69(2):211-7. doi: 10.1016/j.cyto.2014.06.003. Epub 2014 Jul 6.

引用本文的文献

1
Effects of Fasting on THP1 Macrophage Metabolism and Inflammatory Profile.
Int J Mol Sci. 2024 Aug 20;25(16):9029. doi: 10.3390/ijms25169029.
2
Statins and Bempedoic Acid: Different Actions of Cholesterol Inhibitors on Macrophage Activation.
Int J Mol Sci. 2021 Nov 19;22(22):12480. doi: 10.3390/ijms222212480.
3
A data-driven computational model enables integrative and mechanistic characterization of dynamic macrophage polarization.
iScience. 2021 Jan 29;24(2):102112. doi: 10.1016/j.isci.2021.102112. eCollection 2021 Feb 19.
4
Peroxisomes in host defense.
PLoS Pathog. 2020 Jul 2;16(7):e1008636. doi: 10.1371/journal.ppat.1008636. eCollection 2020 Jul.
5
Peroxisomes in Immune Response and Inflammation.
Int J Mol Sci. 2019 Aug 8;20(16):3877. doi: 10.3390/ijms20163877.

本文引用的文献

1
Reshaping of Human Macrophage Polarization through Modulation of Glucose Catabolic Pathways.
J Immunol. 2015 Sep 1;195(5):2442-51. doi: 10.4049/jimmunol.1403045. Epub 2015 Jul 24.
3
Tissue-specific signals control reversible program of localization and functional polarization of macrophages.
Cell. 2014 May 8;157(4):832-44. doi: 10.1016/j.cell.2014.04.016. Epub 2014 May 1.
6
Macrophage plasticity and polarization in tissue repair and remodelling.
J Pathol. 2013 Jan;229(2):176-85. doi: 10.1002/path.4133. Epub 2012 Nov 29.
7
Cell elasticity determines macrophage function.
PLoS One. 2012;7(9):e41024. doi: 10.1371/journal.pone.0041024. Epub 2012 Sep 18.
9
Hemophagocytic macrophages in murine typhoid fever have an anti-inflammatory phenotype.
Infect Immun. 2012 Oct;80(10):3642-9. doi: 10.1128/IAI.00656-12. Epub 2012 Aug 6.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验