Wang Dingchen, Lin Miao, Wang Ruobing, Huang Xiaoran, Liang Yaowen, Wang Xiran, Chen Yuge, Gao Yunfei, Guo Huiming, Liang Huiying, Li Xin
School of Medicine, South China University of Technology, Guangzhou, Guangdong Province, China.
Department of Emergency Medicine, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong Province, China.
J Cell Mol Med. 2025 Feb;29(3):e70366. doi: 10.1111/jcmm.70366.
The relationship between the changes in endothelial cell-cell junctions and microvascular abnormalities in the progression of hypertrophic cardiomyopathy (HCM), as well as their potential as early biomarkers, remains unclear. Here, we analysed single-nucleus RNA-sequencing data from the left ventricles of 44 health donors and HCM patients. First, we observed that endothelial cell-cell junctions were significantly altered in HCM vascular endothelial cells (ECs), including tight junctions, gap junctions and adherens junctions, especially in capillary ECs. The proposed pseudo-timing analysis predicted that endothelial cell-cell junctions abnormalities occurred in the early stages of HCM. Second, we verified that endothelial cell-cell junctions disorders occur at early stages of HCM disease progression in two time-series single-nucleus datasets of mice. The expression of eight cell-cell junction genes showed an initial increase in the early stage, followed by a slight decrease in the middle stage, and a sharp increase in the later stage. Subsequently, cell communication and transcription factor analysis were used to explore the underlying mechanisms. Furthermore, an early HCM prediction model was developed and independently validated using three mRNA datasets comprising 204 health individuals and HCM patients for the eight genes panel, the accuracy was 0.81 [0.63-0.98]. Finally, we validated this panel in HCM tissues. This study demonstrated in humans and mice that eight cell-cell junction genes were significantly elevated in the early stages of HCM and may be potential biomarkers for the early diagnosis of HCM.
肥厚型心肌病(HCM)进展过程中内皮细胞间连接变化与微血管异常之间的关系及其作为早期生物标志物的潜力仍不清楚。在此,我们分析了44名健康供体和HCM患者左心室的单核RNA测序数据。首先,我们观察到HCM血管内皮细胞(ECs)中的内皮细胞间连接发生了显著改变,包括紧密连接、缝隙连接和黏附连接,尤其是在毛细血管ECs中。所提出的伪时间分析预测内皮细胞间连接异常发生在HCM的早期阶段。其次,我们在小鼠的两个时间序列单核数据集中验证了内皮细胞间连接紊乱发生在HCM疾病进展的早期阶段。八个细胞间连接基因的表达在早期阶段最初增加,随后在中期略有下降,在后期急剧增加。随后,使用细胞通讯和转录因子分析来探索潜在机制。此外,开发了一个早期HCM预测模型,并使用包含204名健康个体和HCM患者的三个mRNA数据集对八个基因面板进行了独立验证,准确率为0.81[0.63-0.98]。最后,我们在HCM组织中验证了这个基因面板。这项研究在人类和小鼠中证明,八个细胞间连接基因在HCM早期阶段显著升高,可能是HCM早期诊断的潜在生物标志物。