首页|基于单细胞测序研究心阳片改善尿毒症心肌病心肌纤维化的分子机制

基于单细胞测序研究心阳片改善尿毒症心肌病心肌纤维化的分子机制

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运用单细胞测序技术探究心阳片对尿毒症心肌病(uremic cardiomyopathy,UCM)心肌纤维化的改善作用。采用5/6肾切术(5/6 nephrectomy,NPM)建立UCM小鼠模型,并随机分为模型组、心阳片组,假手术组为对照。心阳片组术后接受心阳片(0。34 g·kg-1)干预。8周后,解离各组小鼠心脏,进行10×Genomics单细胞测序。数据经过t-SNE降维、K-means聚类方法和CellMarker注释后,使用Seurat和Monocle3工具进行差异表达和细胞分化轨迹分析。CellChat工具用于解析细胞间信号通讯。结果显示,该研究共鉴定出成纤维细胞、内皮细胞、免疫细胞等9种细胞。成纤维细胞的单细胞表达结果和基因本体论(Gene Ontology,GO)富集分析显示,心阳片调节心肌纤维化因子和相关信号。拟时序分析结果鉴定出小鼠心脏成纤维细胞主要的3条分化轨迹,并识别分泌型磷酸蛋白1(secreted phosphoprotein 1,Spp1)的表达与成纤维细胞分化轨迹一致。细胞交互网络分析结果表明,与模型组相比,心阳片组小鼠心脏成纤维细胞与其他细胞之间的通讯信号减弱。配体-受体互作分析结果表明,与模型组相比,心阳片组小鼠髓系细胞来源的骨桥蛋白(osteopontin,OPN)与心脏成纤维细胞的相互作用减弱,髓系细胞Spp1配体与心脏成纤维细胞受体之间的相互作用减弱。综上所述,心阳片可能通过抑制内源性和外源性OPN,在单细胞水平上改善UCM心肌纤维化。
Molecular mechanism of Xinyang Tablets in improving myocardial fibrosis in uremic cardiomyopathy based on single-cell sequencing technology
This study aimed to investigate the ameliorative effect of Xinyang Tablets on myocardial fibrosis in uremic cardiomyopathy (UCM) using single-cell sequencing technology.UCM mouse models were established by 5/6 nephrectomy (NPM) and randomly divided into the model group,Xinyang Tablets group,and sham-operated (sham) group as the control.The Xinyang Tablets group received postoperative interventions of Xinyang Tablets (0.34 g·kg-1).After eight weeks,the hearts of the mice in each group were disassociated and subjected to 10×Genomics single-cell sequencing.The data were subjected to t-SNE dimensionality reduction,K-means clustering,and CellMarker annotation prior to analyzing differential expression and cell differentiation trajectories using the Seurat and Monocle3 tools.Additionally,the CellChat tool was used to parse intercellular signaling communication.The results showed that a total of nine types of cells including fibroblasts,endothelial cells,and immune cells were identified in this study.The single-cell expression results of fibroblasts and Gene Ontology (GO) enrichment analysis showed that Xinyang Tablets regulated myocardial fibrosis factors and related signals.Mimetic timing analysis identified three major differentiation trajectories of mouse cardiac fibroblasts and identified the expression of secreted phosphoprotein 1 (Spp1) as consistent with the fibroblast differentiation trajectory.Cellular interaction network analysis showed that the communication signals between mouse cardiac fibroblasts and other cells were weakened in the Xinyang Tablets group compared with the model group.The results of ligand-receptor interaction analysis showed that the interaction between myeloid cell-derived osteopontin (OPN) and cardiac fibroblasts and between myeloid cell Spp1 ligand and cardiac fibroblast receptor of mice in the Xinyang Tablets group was weakened compared with the model group.In conclusion,Xinyang Tablets may improve myocardial fibrosis in UCM by inhibiting both endogenous and exogenous OPN at the single-cell level.

uremic cardiomyopathyXinyang Tabletsosteopontinmyocardial fibrosissingle-cell sequencing

倪世豪、李姿儒、李思静、何星灵、李锦、陈星伶、龙文杰、张维维、廖慧丽、鲁路、杨忠奇

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中医证候全国重点实验室广州中医药大学第一附属医院,广东广州 510407

广州中医药大学岭南医学研究中心,广东广州 510405

广东省中医临床研究院,广东广州 510407

广州中医药大学 第一附属医院老年病科,广东广州 510407

深圳市宝安中医院(集团),广东深圳 518133

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尿毒症心肌病 心阳片 骨桥蛋白 心肌纤维化 单细胞测序

2024

中国中药杂志
中国药学会

中国中药杂志

CSTPCD北大核心
影响因子:1.718
ISSN:1001-5302
年,卷(期):2024.49(24)