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  • 李春雨,何思宇,胡桑宇,等.基于免疫细胞微环境分析不同心肌病的异质性[J].同济大学学报(医学版),2025,46(2):174-184.    [点击复制]
  • LI Chunyu,HE Siyu,HU Sangyu,et al.Identification of heterogeneity in different cardiomyopathies based on immune cell microenvironment[J].Journal of Tongji University(Medical Science),2025,46(2):174-184.   [点击复制]
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基于免疫细胞微环境分析不同心肌病的异质性
李春雨,何思宇,胡桑宇,彭鲁英,李丽
0
(同济大学医学院,上海200331;同济大学心脏病全国重点实验室,上海200120)
摘要:
目的通过心脏免疫细胞的单细胞转录组测序(single cell RNA-sequencing, scRNA-seq)和批量转录组测序(bulk RNA-sequencing, RNA-seq)数据联合分析,探究不同类型心肌病的细胞异质性和免疫细胞微环境变化,为心脏免疫治疗提供一定的依据。 方法从基因表达综合数据库(gene expression omnibus, GEO)获取人类扩张型心肌病(dilated cardiomyopathy, DCM)、肥厚型心肌病(hypertrophic cardiomyopathy, HCM)、缺血性心肌病(ischemic cardiomyopathy, ICM)和健康对照心脏样本的免疫细胞scRNA-seq和RNA-seq数据,使用Seurat、Monocle和clusterProfiler等R包进行单细胞数据分析: 数据整合、差异表达基因(differentially expressed genes, DEGs)筛选、细胞类型鉴定、通路富集和拟时序分析等,利用CIBERSORT进行RNA-seq数据的免疫浸润分析。 结果整合了健康对照和3种心肌病的心脏免疫细胞scRNA-seq数据,优化筛选后获得19 348个细胞,并分为7种免疫细胞类型。分析发现自然杀伤细胞(natural killer cell, NK)在ICM中占比较高,说明NK细胞与心脏炎症高度相关。通过对胸腺依赖淋巴细胞(thymus dependent lymphocyte, T)进行亚型鉴定和拟时序分析,识别了10种T细胞亚型,发现应激反应状态的T细胞仅在ICM中形成拟时序轨迹,并进一步筛选到12个在T细胞各亚型间差异表达并且随拟时序变化的特异性的基因,主要在炎症和免疫调节过程中发挥作用。RNA-seq数据的免疫浸润分析发现,单核细胞(monocyte, MO)在DCM和ICM患者中浸润率较低,CD4+ T细胞和M2巨噬细胞(macrophage, Mφ)在HCM患者中浸润率较低,肥大细胞(mast cell, MC)则在HCM患者中浸润率较高。 结论发现了3种心肌病的免疫细胞异质性和免疫微环境变化,为探索不同心肌病的机制提供了一定的参考依据。
关键词:  单细胞转录组测序  批量转录组测序  免疫细胞  免疫微环境  心肌病
DOI:10.12289/j.issn.2097-4345.24290
通信作者:李丽,E-mail: lilirz@tongji.edu.cn
投稿时间:2024-07-15
录用日期:2024-11-01
基金项目:
Identification of heterogeneity in different cardiomyopathies based on immune cell microenvironment
LI Chunyu,HE Siyu,HU Sangyu,PENG Luying,LI Li
(School of Medicine, Tongji University, Shanghai 200331, China;State Key Laboratory of Cardiology,Shanghai East Hospital, School of Medicine, Tongji University, Shanghai 200120, China)
Abstract:
ObjectiveTo investigate the cell heterogeneity of different types and the changes of immune cell microenvironment of cardiomyopathy by jointly analyzing single cell RNA-sequencing(scRNA-seq) and bulk RNA-sequencing(RNA-seq) so as to provide some basis for cardiac immunotherapy. MethodsHuman immune cell scRNA-seq and RNA-seq data of dilated cardiomyopathy(DCM), hypertrophic cardiomyopathy(HCM), ischemic cardiomyopathy(ICM) and healthy controls were obtained from the Gene Expression Omnibus(GEO) database. The scRNA-seq and RNA-seq data were analyzed using R packages such as Seurat, monocle and clusterProfiler: data integration, differentially expressed genes(DEGs), cell type identification, enrichment analysis and pseudotime-ordered analysis. CIBERSOR was used for immunoinfiltration analysis of RNA-seq data. ResultsThe scRNA-seq data of cardiac immune cells from normal control and three types of cardiomyopathy were integrated, and 19 348 cells were obtained after optimized screening, and were divided into 7 types of immune cells. The high proportion of NK cells in ICM indicated that NK cells were associated with high cardiac inflammation. The T cells including ten subtypes identified by subtype identification and pseudotime-ordered analysis. It was found that T cells in stress response state only seemed to form a pseudo-temporal locus in ICM, and 12 specific genes of DEGs among T cell subtypes with pseudo-temporal variation were screened, which played a role in the process of inflammation and immune regulation. Immunoinfiltration analysis of RNA-seq data showed that monocytes had a low infiltration rate in DCM and ICM patients, CD4+T cells and M2 macrophages had a low infiltration rate in HCM patients, and mast cells had a high infiltration rate in HCM patients. ConclusionThe heterogeneity of immune cells and the changes of immune microenvironment in three kinds of cardiomyopathy are found in this study, which provide a certain reference for exploring the mechanism of different cardiomyopathy.
Key words:  single cell RNA-sequencing  bulk RNA-sequencing  immune cells  immune microenvironment  cardiomyopathy

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