Hoffman Jessica R, Jayaraman Arun R, Bheri Sruti, Davis Michael E
Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology & Emory University School of Medicine, Atlanta, GA 30322, USA.
Molecular & Systems Pharmacology Graduate Training Program, Graduate Division of Biological & Biomedical Sciences, Laney Graduate School, Emory University, Atlanta, GA 30322, USA.
J Cardiovasc Dev Dis. 2022 Nov 1;9(11):374. doi: 10.3390/jcdd9110374.
Human cardiac-derived c-kit+ stromal cells (CSCs) have demonstrated efficacy in preclinical trials for the treatment of heart failure and myocardial dysfunction. Unfortunately, large variability in patient outcomes and cell populations remains a problem. Previous research has demonstrated that the reparative capacity of CSCs may be linked to the age of the cells: CSCs derived from neonate patients increase cardiac function and reduce fibrosis. However, age-dependent differences between CSC populations have primarily been explored with bulk sequencing methods. In this work, we hypothesized that differences in CSC populations and subsequent cell therapy outcomes may arise from differing cell subtypes within donor CSC samples. We performed single-cell RNA sequencing on four neonatal CSC (nCSC) and five child CSC (cCSC) samples. Subcluster analysis revealed cCSC-enriched clusters upregulated in several fibrosis- and immune response-related genes. Module-based analysis identified upregulation of chemotaxis and ribosomal activity-related genes in nCSCs and upregulation of immune response and fiber synthesis genes in cCSCs. Further, we identified versican and integrin alpha 2 as potential markers for a fibrotic cell subtype. By investigating differences in patient-derived CSC populations at the single-cell level, this research aims to identify and characterize CSC subtypes to better optimize CSC-based therapy and improve patient outcomes.
人心脏来源的c-kit+基质细胞(CSCs)在治疗心力衰竭和心肌功能障碍的临床前试验中已显示出疗效。不幸的是,患者预后和细胞群体的巨大变异性仍然是一个问题。先前的研究表明,CSCs的修复能力可能与细胞年龄有关:来自新生儿患者的CSCs可改善心脏功能并减少纤维化。然而,CSC群体之间的年龄依赖性差异主要是通过批量测序方法进行探索的。在这项研究中,我们假设CSC群体的差异以及随后的细胞治疗结果可能源于供体CSC样本中不同的细胞亚型。我们对四个新生儿CSC(nCSC)和五个儿童CSC(cCSC)样本进行了单细胞RNA测序。亚群分析显示,cCSC富集的簇在几个与纤维化和免疫反应相关的基因中上调。基于模块的分析确定了nCSCs中趋化性和核糖体活性相关基因的上调以及cCSCs中免疫反应和纤维合成基因的上调。此外,我们确定versican和整合素α2是纤维化细胞亚型的潜在标志物。通过在单细胞水平上研究患者来源的CSC群体的差异,本研究旨在识别和表征CSC亚型,以更好地优化基于CSC的治疗并改善患者预后。