N-CADHERIN+/CD168- subpopulation determines therapeutic variations of UC-MSCs for cardiac repair after myocardial infarction.

IF 7.1 2区 医学 Q1 CELL & TISSUE ENGINEERING Stem Cell Research & Therapy Pub Date : 2024-11-13 DOI:10.1186/s13287-024-04032-4
Yukang Wu, Jianguo Li, Ke Feng, Ailing Tan, Yingying Gao, Wen Chen, Wenwen Jia, Xudong Guo, Jiuhong Kang
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Abstract

Background: The efficiency of mesenchymal stem cells (MSCs) in treating myocardial infarction (MI) remains inconsistent, which limits their therapeutic applications. Therefore, exploring the mechanism for the inconsistent efficacy of MSCs and identification the criteria for screening MSCs are important for improving the efficiency of MSCs.

Methods: Mouse model after MI was utilized to test the role of MSCs from different donors and the functional subpopulation in improving cardiac function. Heterogeneity of MSCs was identified using single-cell RNA sequencing (scRNA-seq) of MSC-GY. GSEA and Scissor analyses were used to find the functional subpopulations of MSCs that promote angiogenesis. The role of functional subpopulations in promoting angiogenesis was verified by detecting the secretory proteins, the ratio of N-CADHERIN+/CD168- subpopulations in MSCs, and the tube formation, migration, and proliferation of HUVECs after treatment with conditional medium (CM) derived from different MSCs.

Results: We found that umbilical cord-derived MSCs (UC-MSCs) from different donors have varied therapeutic efficacy in MI mice and UC-MSCs with higher therapeutic effectiveness exhibited the most potent pro-angiogenic effects by secreting elevated levels of angiogenesis-related proteins, such as MYDGF, VEGFA, and FGF2. ScRNA-seq of 10,463 UC-MSCs revealed that the N-CADHERIN+/CD168- subpopulation was closely associated with pro-angiogenic effects, and the ratio of this cell subpopulation was positively correlated with the angiogenic potential of MSCs. We also found that the N-CADHERIN+/CD168- subpopulation was the functional subpopulation of MSCs in improving cardiac function of MI mice.

Conclusions: Our study identified that the N-CADHERIN+/CD168- subpopulation was the functional subpopulation of MSCs in treating MI, which was essential for the development and utilization of MSCs in MI treatment.

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N-CADHERIN+/CD168- 亚群决定了 UC-间充质干细胞在心肌梗塞后心脏修复中的治疗变化。
背景:间充质干细胞(MSCs)治疗心肌梗死(MI)的疗效仍不一致,这限制了其治疗应用。因此,探索间充质干细胞疗效不一致的机制并确定筛选间充质干细胞的标准对提高间充质干细胞的疗效非常重要:方法:利用心肌梗死后的小鼠模型测试不同供体的间充质干细胞和功能亚群在改善心脏功能方面的作用。利用间充质干细胞-GY的单细胞RNA测序(scRNA-seq)确定了间充质干细胞的异质性。利用GSEA和Scissor分析找到了促进血管生成的间充质干细胞功能亚群。通过检测间充质干细胞的分泌蛋白、N-CADHERIN+/CD168-亚群的比例,以及不同间充质干细胞衍生的条件培养基(CM)处理后HUVECs的管形成、迁移和增殖,验证了功能亚群在促进血管生成中的作用:结果:我们发现来自不同供体的脐带间充质干细胞(UC-MSCs)对心肌梗死小鼠有不同的疗效,疗效较高的 UC-MSCs 能分泌更高水平的血管生成相关蛋白,如 MYDGF、VEGFA 和 FGF2,从而表现出最强的促血管生成作用。对 10,463 个 UC-MSCs 进行的 ScRNA 序列分析表明,N-CADHERIN+/CD168-亚群与促血管生成效应密切相关,而且该细胞亚群的比例与间充质干细胞的血管生成潜能呈正相关。我们还发现,N-CADHERIN+/CD168-亚群是间充质干细胞改善心肌梗死小鼠心脏功能的功能亚群:我们的研究发现,N-CADHERIN+/CD168-亚群是间充质干细胞治疗心肌梗死的功能亚群,这对开发和利用间充质干细胞治疗心肌梗死至关重要。
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来源期刊
Stem Cell Research & Therapy
Stem Cell Research & Therapy CELL BIOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
CiteScore
13.20
自引率
8.00%
发文量
525
审稿时长
1 months
期刊介绍: Stem Cell Research & Therapy serves as a leading platform for translational research in stem cell therapies. This international, peer-reviewed journal publishes high-quality open-access research articles, with a focus on basic, translational, and clinical research in stem cell therapeutics and regenerative therapies. Coverage includes animal models and clinical trials. Additionally, the journal offers reviews, viewpoints, commentaries, and reports.
期刊最新文献
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