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HIV 和 SARS-CoV-2 感染中髓样细胞功能的表观遗传调控。

Epigenetic modulation of myeloid cell functions in HIV and SARS-CoV-2 infection.

机构信息

Institute of Clinical Chemistry and Clinical Pharmacology, University Hospital Bonn, 53127, Bonn, Germany.

Department of Microbiology and Immunology, the Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, VIC, 3000, Australia.

出版信息

Mol Biol Rep. 2024 Feb 24;51(1):342. doi: 10.1007/s11033-024-09266-2.


DOI:10.1007/s11033-024-09266-2
PMID:38400997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10894183/
Abstract

Myeloid cells play a vital role in innate immune responses as they recognize and phagocytose pathogens like viruses, present antigens, produce cytokines, recruit other immune cells to combat infections, and contribute to the attenuation of immune responses to restore homeostasis. Signal integration by pathogen recognition receptors enables myeloid cells to adapt their functions by a network of transcription factors and chromatin remodelers. This review provides a brief overview of the subtypes of myeloid cells and the main epigenetic regulation mechanisms. Special focus is placed on the epigenomic alterations in viral nucleic acids of HIV and SARS-CoV-2 along with the epigenetic changes in the host's myeloid cell compartment. These changes are important as they lead to immune suppression and promote the progression of the disease. Finally, we highlight some promising examples of 'epidrugs' that modulate the epigenome of immune cells and could be used as therapeutics for viral infections.

摘要

髓样细胞在先天免疫反应中起着至关重要的作用,因为它们能够识别和吞噬病毒等病原体,呈递抗原,产生细胞因子,招募其他免疫细胞来对抗感染,并有助于减轻免疫反应以恢复体内平衡。病原体识别受体的信号整合使髓样细胞能够通过转录因子和染色质重塑剂网络来适应其功能。本综述简要概述了髓样细胞的亚型和主要的表观遗传调控机制。特别关注 HIV 和 SARS-CoV-2 病毒核酸中的表观基因组改变以及宿主髓样细胞区室中的表观遗传改变。这些变化很重要,因为它们导致免疫抑制并促进疾病的进展。最后,我们强调了一些有前途的“epidrug”范例,这些范例可以调节免疫细胞的表观基因组,并可用于治疗病毒感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a890/10894183/0d83f2b990a8/11033_2024_9266_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a890/10894183/3ddf9932605c/11033_2024_9266_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a890/10894183/dc42d2083a07/11033_2024_9266_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a890/10894183/a0e6b58be30f/11033_2024_9266_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a890/10894183/781b54da2b80/11033_2024_9266_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a890/10894183/0d83f2b990a8/11033_2024_9266_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a890/10894183/3ddf9932605c/11033_2024_9266_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a890/10894183/dc42d2083a07/11033_2024_9266_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a890/10894183/a0e6b58be30f/11033_2024_9266_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a890/10894183/781b54da2b80/11033_2024_9266_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a890/10894183/0d83f2b990a8/11033_2024_9266_Fig5_HTML.jpg

相似文献

[1]
Epigenetic modulation of myeloid cell functions in HIV and SARS-CoV-2 infection.

Mol Biol Rep. 2024-2-24

[2]
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Eur Rev Med Pharmacol Sci. 2021-10

[3]
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Pathogens. 2025-2-1

[4]
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Biochim Biophys Acta Mol Basis Dis. 2023-3

[5]
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J Leukoc Biol. 2021-7

[6]
Epigenetic Lens to Visualize the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) Infection in COVID-19 Pandemic.

Front Genet. 2021-3-22

[7]
SARS-CoV-2 exacerbates proinflammatory responses in myeloid cells through C-type lectin receptors and Tweety family member 2.

Immunity. 2021-6-8

[8]
SARS-CoV-2 Modulation of HIV Latency Reversal in a Myeloid Cell Line: Direct and Bystander Effects.

Viruses. 2024-8-17

[9]
The emerging role of SARS-CoV-2 nonstructural protein 1 (nsp1) in epigenetic regulation of host gene expression.

FEMS Microbiol Rev. 2024-9-18

[10]
Targeting Myeloid Differentiation Primary Response Protein 88 (MyD88) and Galectin-3 to Develop Broad-Spectrum Host-Mediated Therapeutics against SARS-CoV-2.

Int J Mol Sci. 2024-8-1

引用本文的文献

[1]
HIV-Induced Sialoglycans on Infected Cells Promote Immune Evasion from Myeloid Cell-Mediated Killing.

bioRxiv. 2025-2-27

[2]
An Epigenetic Locus Associated with Loss of Smell in COVID-19.

Diagnostics (Basel). 2024-12-15

[3]
Is There such a Thing as Post-Viral Depression?: Implications for Precision Medicine.

Biomol Ther (Seoul). 2024-11-1

本文引用的文献

[1]
Paired ATAC- and RNA-seq offer insight into the impact of HIV on alveolar macrophages: a pilot study.

Sci Rep. 2023-9-15

[2]
Prevalence and impact of myocardial injury among patients hospitalized with COVID-19.

Front Cardiovasc Med. 2023-8-1

[3]
A high-throughput screening assay for silencing established HIV-1 macrophage infection identifies nucleoside analogs that perturb H3K9me3 on proviral genomes.

J Virol. 2023-8-31

[4]
Integration of gene expression and DNA methylation data across different experiments.

Nucleic Acids Res. 2023-8-25

[5]
CD4 T cell calibration of antigen-presenting cells optimizes antiviral CD8 T cell immunity.

Nat Immunol. 2023-6

[6]
The generation, activation, and polarization of monocyte-derived macrophages in human malignancies.

Front Immunol. 2023

[7]
SARS-CoV-2 restructures host chromatin architecture.

Nat Microbiol. 2023-4

[8]
Tissue-specific macrophages: how they develop and choreograph tissue biology.

Nat Rev Immunol. 2023-9

[9]
Spatial epigenome-transcriptome co-profiling of mammalian tissues.

Nature. 2023-4

[10]
A methylation clock model of mild SARS-CoV-2 infection provides insight into immune dysregulation.

Mol Syst Biol. 2023-5-9

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