Single-cell and spatial heterogeneity landscapes of mature epicardial cells

被引:10
作者
Du, Jianlin [1 ]
Yuan, Xin [2 ]
Deng, Haijun [3 ]
Huang, Rongzhong [4 ]
Liu, Bin [1 ]
Xiong, Tianhua [1 ]
Long, Xianglin [1 ]
Zhang, Ling [5 ]
Li, Yingrui [1 ]
She, Qiang [1 ]
机构
[1] Chongqing Med Univ, Dept Cardiol, Affiliated Hosp 2, Chongqing 400010, Peoples R China
[2] Chongqing Med Univ, Dept Nephrol, Affiliated Hosp 2, Chongqing 400010, Peoples R China
[3] Chongqing Med Univ, Inst Viral Hepatitis, Key Lab Mol Biol Infect Dis, Minist Educ,Affiliated Hosp 2, Chongqing 400010, Peoples R China
[4] Chongqing Med Univ, Precis Med Ctr, Affiliated Hosp 2, Chongqing 400010, Peoples R China
[5] Chongqing Med Univ, Basic Med Res & Innovat Ctr Novel Target & Therap, Minist Educ, Affiliated Hosp 2, Chongqing 400010, Peoples R China
基金
中国国家自然科学基金;
关键词
Epicardial cells; Gene markers; Single-cell sequencing; Spatial transcriptomics; EXTRACELLULAR-MATRIX PROTEINS; IN-SITU HYBRIDIZATION; UROTHELIAL DIFFERENTIATION; MYOCARDIAL-INFARCTION; HEART REGENERATION; PROGENITOR CELLS; MOUSE EMBRYOS; STEM-CELLS; EXPRESSION; CLONING;
D O I
10.1016/j.jpha.2023.07.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tbx18, Wt1, and Tcf21 have been identified as epicardial markers during the early embryonic stage. However, the gene markers of mature epicardial cells remain unclear. Single-cell transcriptomic analysis was performed with the Seurat, Monocle, and CellphoneDB packages in R software with standard procedures. Spatial transcriptomics was performed on chilled Visium Tissue Optimization Slides (10x Genomics) and Visium Spatial Gene Expression Slides (10x Genomics). Spatial transcriptomics analysis was performed with Space Ranger software and R software. Immunofluorescence, whole-mount RNA in situ hybridization and X-gal staining were performed to validate the analysis results. Spatial transcriptomics analysis revealed distinct transcriptional profiles and functions between epicardial tissue and non-epicardial tissue. Several gene markers specific to postnatal epicardial tissue were identified, including Msln, C3, Efemp1, and Upk3b. Single-cell transcriptomic analysis revealed that cardiac cells from wildtype mouse hearts (from embryonic day 9.5 to postnatal day 9) could be categorized into six major cell types, which included epicardial cells. Throughout epicardial development, Wt1, Tbx18, and Upk3b were consistently expressed, whereas genes including Msln, C3, and Efemp1 exhibited increased expression during the mature stages of development. Pseudotime analysis further revealed two epicardial cell fates during maturation. Moreover, Upk3b, Msln, Efemp1, and C3 positive epicardial cells were enriched in extracellular matrix signaling. Our results suggested Upk3b, Efemp1, Msln, C3, and other genes were mature epicardium markers. Extracellular matrix signaling was found to play a critical role in the mature epicardium, thus suggesting potential therapeutic targets for heart regeneration in future clinical practice. (c) 2023 The Author(s). Published by Elsevier B.V. on behalf of Xi'an Jiaotong University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:894 / 907
页数:14
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