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鉴定 HIV-1 和肺动脉高压之间的共享枢纽基因特征和分子机制。

Identification of the shared hub gene signatures and molecular mechanisms between HIV-1 and pulmonary arterial hypertension.

机构信息

School of Public Health, Guangxi Medical University, Nanning, 530021, China.

Guangxi Key Laboratory of AIDS Prevention and Treatment, Guangxi Medical University, Nanning, 530021, China.

出版信息

Sci Rep. 2024 Mar 25;14(1):7048. doi: 10.1038/s41598-024-55645-x.


DOI:10.1038/s41598-024-55645-x
PMID:38528047
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10963360/
Abstract

The close link between HIV-1 infection and the occurrence of pulmonary arterial hypertension (PAH). However, the underlying molecular mechanisms of their interrelation remain unclear. The microarray data of HIV-1 and PAH were downloaded from GEO database. We utilized WGCNA to identify shared genes between HIV-1 and PAH, followed by conducting GO and pathway enrichment analyses. Subsequently, differentially genes analysis was performed using external validation datasets to further filter hub genes. Immunoinfiltration analysis was performed using CIBERSORT. Finally, hub gene expression was validated using scRNA-seq data. We identified 109 shared genes through WGCNA, primarily enriched in type I interferon (IFN) pathways. By taking the intersection of WGCNA important module genes and DEGs, ISG15 and IFI27 were identified as pivotal hub genes. Immunoinfiltration analysis and scRNA-seq results indicated the significant role of monocytes in the shared molecular mechanisms of HIV-1 and PAH. In summary, our study illustrated the possible mechanism of PAH secondary to HIV-1 and showed that the heightened IFN response in HIV-1 might be a crucial susceptibility factor for PAH, with monocytes being pivotal cells involved in the type I IFN response pathway. This provides potential new insights for further investigating the molecular mechanisms connecting HIV-1 and PAH.

摘要

HIV-1 感染与肺动脉高压(PAH)的发生密切相关。然而,它们相互关系的潜在分子机制尚不清楚。从 GEO 数据库中下载了 HIV-1 和 PAH 的微阵列数据。我们利用 WGCNA 来识别 HIV-1 和 PAH 之间的共享基因,然后进行 GO 和通路富集分析。随后,使用外部验证数据集进行差异基因分析,以进一步筛选枢纽基因。使用 CIBERSORT 进行免疫浸润分析。最后,使用 scRNA-seq 数据验证枢纽基因的表达。通过 WGCNA 我们确定了 109 个共享基因,主要富集在 I 型干扰素(IFN)途径中。通过取 WGCNA 重要模块基因和 DEGs 的交集,确定 ISG15 和 IFI27 为关键枢纽基因。免疫浸润分析和 scRNA-seq 结果表明单核细胞在 HIV-1 和 PAH 的共享分子机制中起着重要作用。总之,我们的研究说明了 HIV-1 继发 PAH 的可能机制,并表明 HIV-1 中增强的 IFN 反应可能是 PAH 的一个关键易感因素,单核细胞是参与 I 型 IFN 反应途径的关键细胞。这为进一步研究 HIV-1 和 PAH 之间的分子机制提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/fb39dbc1e939/41598_2024_55645_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/a6ac53c963b9/41598_2024_55645_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/fba4a418bd3b/41598_2024_55645_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/1e83c2f2fe0a/41598_2024_55645_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/003b553c2e7c/41598_2024_55645_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/defdf6aba0aa/41598_2024_55645_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/cd918e3b140e/41598_2024_55645_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/0705d112f462/41598_2024_55645_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/fb39dbc1e939/41598_2024_55645_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/a6ac53c963b9/41598_2024_55645_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/fba4a418bd3b/41598_2024_55645_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/1e83c2f2fe0a/41598_2024_55645_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/003b553c2e7c/41598_2024_55645_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/defdf6aba0aa/41598_2024_55645_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/cd918e3b140e/41598_2024_55645_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/0705d112f462/41598_2024_55645_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c84/10963360/fb39dbc1e939/41598_2024_55645_Fig8_HTML.jpg

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本文引用的文献

[1]
Designing a Next-Generation Multiepitope-Based Vaccine against Using Reverse Vaccinology Approaches.

Pathogens. 2023-2-25

[2]
Blood transcriptome analysis revealed the crosstalk between COVID-19 and HIV.

Front Immunol. 2022

[3]
Single-cell sequencing resolves the landscape of immune cells and regulatory mechanisms in HIV-infected immune non-responders.

Cell Death Dis. 2022-10-4

[4]
Membrane Protein OTOF Is a Type I Interferon-Induced Entry Inhibitor of HIV-1 in Macrophages.

mBio. 2022-8-30

[5]
Type I interferons and TGF-β cooperate to induce liver fibrosis during HIV-1 infection under antiretroviral therapy.

JCI Insight. 2022-7-8

[6]
Epigenetic Regulation of IFI44L Expression in Monocytes Affects the Functions of Monocyte-Derived Dendritic Cells in Systemic Lupus Erythematosus.

J Immunol Res. 2022

[7]
Peripheral blood CD4CCR6 compartment differentiates HIV-1 infected or seropositive elite controllers from long-term successfully treated individuals.

Commun Biol. 2022-4-13

[8]
Immune Cells in Pulmonary Arterial Hypertension.

Heart Lung Circ. 2022-7

[9]
Comparative Transcriptional Analysis Identified Characteristic Genes and Patterns in HIV-Infected Immunological Non-Responders.

Front Immunol. 2022

[10]
Exploring capsule polysaccharide proteins to design multiepitope subunit vaccine to fight against pneumonia.

Expert Rev Vaccines. 2022-4

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