Uncovering SPP1+ Macrophage, Neutrophils and Their Related Diagnostic Biomarkers in Intracranial Aneurysm and Subarachnoid Hemorrhage.

IF 4.2 2区 医学 Q2 IMMUNOLOGY
Journal of Inflammation Research Pub Date : 2024-11-09 eCollection Date: 2024-01-01 DOI:10.2147/JIR.S493828
Haipeng Jie, Boyang Wang, Jingjing Zhang, Xinzhao Wang, Xiang Song, Fan Yang, Changning Fu, Bo Dong, Feng Yan
{"title":"Uncovering SPP1<sup>+</sup> Macrophage, Neutrophils and Their Related Diagnostic Biomarkers in Intracranial Aneurysm and Subarachnoid Hemorrhage.","authors":"Haipeng Jie, Boyang Wang, Jingjing Zhang, Xinzhao Wang, Xiang Song, Fan Yang, Changning Fu, Bo Dong, Feng Yan","doi":"10.2147/JIR.S493828","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Intracranial aneurysms (IA) frequently cause subarachnoid hemorrhage (SAH) and have poor prognosis. However, the molecular mechanisms and diagnostic biomarkers associated with IA and ruptured IA (rIA) remain poorly understood.</p><p><strong>Methods: </strong>In this study, single-cell and transcriptome datasets were obtained from the GEO database. The cell populations were annotated to identify potential pathogenic subpopulations, followed by intercellular communication, pseudotime, and SCENIC analyses. Proteome-wide and transcriptome-wide Mendelian randomization (MR) analyses were conducted to identify risk factors for IA and SAH. The major pathological changes and diagnostic biomarkers of IA and SAH were identified based on the transcriptome datasets. A clinical cohort was established to identify the diagnostic biomarkers and validate the results.</p><p><strong>Results: </strong>Macrophages and neutrophils were predominantly increased in IA and rIA tissues, and neutrophils were markedly upregulated in the blood of SAH patients. SPP1<sup>+</sup> Macrophage was progressively elevated in aneurysms, promoting vascular smooth muscle cell (VSMC) phenotypic transformation and collagen matrix remodeling through the SPP1 and TGF-β pathways. Furthermore, HIF1α regulon was enriched in SPP1<sup>+</sup> Macrophage, mediating inflammation and metabolic reprogramming, which contributed to IA progression. Integrated MR analysis identified CD36 as a risk factor for both IA and SAH, and it has been recognized as an effective blood biomarker for SAH. Neutrophils and their related indicators have emerged as excellent biomarkers of SAH in clinical cohorts.</p><p><strong>Conclusion: </strong>This study highlighted the detrimental role of SPP1<sup>+</sup> Macrophage in IA and SAH using single-cell sequencing and MR analyses. CD36 was identified as a risk factor for IA and SAH and was also an efficient blood biomarker for SAH. In a clinical cohort, neutrophils and related indicators were valuable for the early diagnosis of SAH.</p>","PeriodicalId":16107,"journal":{"name":"Journal of Inflammation Research","volume":"17 ","pages":"8569-8587"},"PeriodicalIF":4.2000,"publicationDate":"2024-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11559423/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Inflammation Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/JIR.S493828","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Intracranial aneurysms (IA) frequently cause subarachnoid hemorrhage (SAH) and have poor prognosis. However, the molecular mechanisms and diagnostic biomarkers associated with IA and ruptured IA (rIA) remain poorly understood.

Methods: In this study, single-cell and transcriptome datasets were obtained from the GEO database. The cell populations were annotated to identify potential pathogenic subpopulations, followed by intercellular communication, pseudotime, and SCENIC analyses. Proteome-wide and transcriptome-wide Mendelian randomization (MR) analyses were conducted to identify risk factors for IA and SAH. The major pathological changes and diagnostic biomarkers of IA and SAH were identified based on the transcriptome datasets. A clinical cohort was established to identify the diagnostic biomarkers and validate the results.

Results: Macrophages and neutrophils were predominantly increased in IA and rIA tissues, and neutrophils were markedly upregulated in the blood of SAH patients. SPP1+ Macrophage was progressively elevated in aneurysms, promoting vascular smooth muscle cell (VSMC) phenotypic transformation and collagen matrix remodeling through the SPP1 and TGF-β pathways. Furthermore, HIF1α regulon was enriched in SPP1+ Macrophage, mediating inflammation and metabolic reprogramming, which contributed to IA progression. Integrated MR analysis identified CD36 as a risk factor for both IA and SAH, and it has been recognized as an effective blood biomarker for SAH. Neutrophils and their related indicators have emerged as excellent biomarkers of SAH in clinical cohorts.

Conclusion: This study highlighted the detrimental role of SPP1+ Macrophage in IA and SAH using single-cell sequencing and MR analyses. CD36 was identified as a risk factor for IA and SAH and was also an efficient blood biomarker for SAH. In a clinical cohort, neutrophils and related indicators were valuable for the early diagnosis of SAH.

揭示颅内动脉瘤和蛛网膜下腔出血的 SPP1+ 巨噬细胞、中性粒细胞及其相关诊断生物标志物
背景:颅内动脉瘤(IA)经常导致蛛网膜下腔出血(SAH),且预后不良。然而,人们对与颅内动脉瘤和破裂颅内动脉瘤(rIA)相关的分子机制和诊断生物标志物仍然知之甚少:本研究从 GEO 数据库中获取了单细胞和转录组数据集。对细胞群进行注释以确定潜在的致病亚群,然后进行细胞间通讯、伪时间和 SCENIC 分析。对整个蛋白质组和整个转录组进行了孟德尔随机化(MR)分析,以确定IA和SAH的风险因素。根据转录组数据集确定了IA和SAH的主要病理变化和诊断生物标志物。建立了临床队列以确定诊断生物标志物并验证结果:结果:IA和rIA组织中巨噬细胞和中性粒细胞主要增加,SAH患者血液中中性粒细胞明显上调。SPP1+巨噬细胞在动脉瘤中逐渐升高,通过SPP1和TGF-β途径促进血管平滑肌细胞(VSMC)表型转化和胶原基质重塑。此外,SPP1+巨噬细胞中富含HIF1α调控因子,介导炎症和代谢重编程,从而导致内皮瘤进展。综合磁共振分析发现,CD36是IA和SAH的危险因素,它已被认为是SAH的有效血液生物标志物。在临床队列中,中性粒细胞及其相关指标已成为SAH的优秀生物标志物:本研究通过单细胞测序和磁共振分析,强调了SPP1+巨噬细胞在IA和SAH中的有害作用。CD36被确定为IA和SAH的危险因素,也是SAH的有效血液生物标志物。在临床队列中,中性粒细胞和相关指标对早期诊断 SAH 很有价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信