Suppr超能文献

组织特异性信号控制巨噬细胞定位和功能极化的可逆程序。

Tissue-specific signals control reversible program of localization and functional polarization of macrophages.

机构信息

Howard Hughes Medical Institute and Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520, USA.

Howard Hughes Medical Institute and Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520, USA.

出版信息

Cell. 2014 May 8;157(4):832-44. doi: 10.1016/j.cell.2014.04.016. Epub 2014 May 1.

Abstract

Tissue-resident macrophages are highly heterogeneous in terms of their functions and phenotypes as a consequence of adaptation to different tissue environments. Local tissue-derived signals are thought to control functional polarization of resident macrophages; however, the identity of these signals remains largely unknown. It is also unknown whether functional heterogeneity is a result of irreversible lineage-specific differentiation or a consequence of continuous but reversible induction of diverse functional programs. Here, we identified retinoic acid as a signal that induces tissue-specific localization and functional polarization of peritoneal macrophages through the reversible induction of transcription factor GATA6. We further found that GATA6 in macrophages regulates gut IgA production through peritoneal B-1 cells. These results provide insight into the regulation of tissue-resident macrophage functional specialization by tissue-derived signals.

摘要

组织驻留巨噬细胞因其适应不同组织环境的功能和表型而具有高度异质性。局部组织来源的信号被认为控制着驻留巨噬细胞的功能极化;然而,这些信号的身份在很大程度上仍然未知。也不知道功能异质性是不可逆的谱系特异性分化的结果,还是连续但可逆的诱导不同功能程序的结果。在这里,我们确定维甲酸是一种信号,通过可逆诱导转录因子 GATA6,诱导腹腔巨噬细胞的组织特异性定位和功能极化。我们进一步发现巨噬细胞中的 GATA6 通过腹膜 B-1 细胞调节肠道 IgA 的产生。这些结果为组织来源的信号调节组织驻留巨噬细胞功能特化提供了深入的了解。

相似文献

1
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.
2
Gata6 regulates aspartoacylase expression in resident peritoneal macrophages and controls their survival.
J Exp Med. 2014 Jul 28;211(8):1525-31. doi: 10.1084/jem.20140570. Epub 2014 Jul 14.
3
Macrophages: Peritoneal population depends on GATA6.
Nat Rev Immunol. 2014 Jun;14(6):360. doi: 10.1038/nri3695.
4
A Stromal Niche Defined by Expression of the Transcription Factor WT1 Mediates Programming and Homeostasis of Cavity-Resident Macrophages.
Immunity. 2019 Jul 16;51(1):119-130.e5. doi: 10.1016/j.immuni.2019.05.010. Epub 2019 Jun 20.
5
mTORC2 Signaling Selectively Regulates the Generation and Function of Tissue-Resident Peritoneal Macrophages.
Cell Rep. 2017 Sep 5;20(10):2439-2454. doi: 10.1016/j.celrep.2017.08.046.
8
The involvement of peritoneal GATA6 macrophages in the pathogenesis of endometriosis.
Front Immunol. 2024 Aug 12;15:1396000. doi: 10.3389/fimmu.2024.1396000. eCollection 2024.
9
The transcription factor Gata6 links tissue macrophage phenotype and proliferative renewal.
Science. 2014 May 9;344(6184):645-648. doi: 10.1126/science.1251414. Epub 2014 Apr 24.

引用本文的文献

1
Inhibition of VEGFR1 TK Signaling in Peritoneal Macrophages Suppresses Endometriosis Development.
In Vivo. 2025 Sep-Oct;39(5):2584-2598. doi: 10.21873/invivo.14059.
2
RNA mA modification: a key regulator in normal and malignant processes.
Cell Investig. 2025 Jun;1(2). doi: 10.1016/j.clnves.2025.100023. Epub 2025 Jun 6.
5
Perivascular Tertiary Lymphoid Structures in Autoimmune Disease.
Immunol Rev. 2025 Jul;332(1):e70047. doi: 10.1111/imr.70047.
6
The Role of Autophagy in the Regulation of Bidirectional Relationships in Diabetic Periodontitis.
J Inflamm Res. 2025 Jun 13;18:7781-7794. doi: 10.2147/JIR.S533791. eCollection 2025.
7
Kupffer cell programming by maternal obesity triggers fatty liver disease.
Nature. 2025 Jun 18. doi: 10.1038/s41586-025-09190-w.
8
Tissue signatures of human macrophages during homeostasis and activation.
bioRxiv. 2025 May 28:2025.05.23.655632. doi: 10.1101/2025.05.23.655632.
9
MODELING TISSUE-RESIDENT MACROPHAGE DEVELOPMENT FROM MOUSE PLURIPOTENT STEM CELLS.
bioRxiv. 2025 May 13:2025.05.01.651743. doi: 10.1101/2025.05.01.651743.

本文引用的文献

1
Adaptation of innate lymphoid cells to a micronutrient deficiency promotes type 2 barrier immunity.
Science. 2014 Jan 24;343(6169):432-7. doi: 10.1126/science.1247606.
2
The epigenomics of embryonic stem cell differentiation.
Int J Biol Sci. 2013 Dec 9;9(10):1134-44. doi: 10.7150/ijbs.7998. eCollection 2013.
3
An intrinsic propensity of murine peritoneal B1b cells to switch to IgA in presence of TGF-β and retinoic acid.
PLoS One. 2013 Dec 6;8(12):e82121. doi: 10.1371/journal.pone.0082121. eCollection 2013.
4
Identification of a tissue-specific, C/EBPβ-dependent pathway of differentiation for murine peritoneal macrophages.
J Immunol. 2013 Nov 1;191(9):4665-75. doi: 10.4049/jimmunol.1300581. Epub 2013 Sep 27.
5
Tissue-resident macrophages.
Nat Immunol. 2013 Oct;14(10):986-95. doi: 10.1038/ni.2705. Epub 2013 Sep 18.
6
The nuclear receptor LXRα controls the functional specialization of splenic macrophages.
Nat Immunol. 2013 Aug;14(8):831-9. doi: 10.1038/ni.2622. Epub 2013 Jun 16.
7
Macrophage biology in development, homeostasis and disease.
Nature. 2013 Apr 25;496(7446):445-55. doi: 10.1038/nature12034.
8
Retinoic acid promotes the development of Arg1-expressing dendritic cells for the regulation of T-cell differentiation.
Eur J Immunol. 2013 Apr;43(4):967-78. doi: 10.1002/eji.201242772. Epub 2013 Feb 14.
10
A lineage of myeloid cells independent of Myb and hematopoietic stem cells.
Science. 2012 Apr 6;336(6077):86-90. doi: 10.1126/science.1219179. Epub 2012 Mar 22.

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