髓样
髓系细胞
医学
癌症研究
心室重构
人口
炎症
心力衰竭
细胞
纤维化
心肌梗塞
骨髓生成
细胞生物学
细胞因子
纤维细胞
生物
趋化因子
心脏纤维化
免疫学
电池类型
心肌纤维化
核糖核酸
趋化性
心功能曲线
促炎细胞因子
细胞培养
内科学
肿瘤坏死因子α
受体
细胞凋亡
作者
Masashi Tomimatsu,Masanori Obana,Shota Tanaka,Ryota Kajiura,Ryoko Nagano,Kotaro Matsumoto,Kosei Yokota,Shunsuke Kominami,Taro Ito,Shota Suzuki,Daisuke Motooka,Yu‐Chen Liu,Shigeto Seno,Daisuke Okuzaki,Izumi Nagatomo,Makiko Maeda,So‐ichiro Fukada,Yoshiaki Okada,Yasushi Fujio
出处
期刊:American Journal of Physiology-heart and Circulatory Physiology
[American Physical Society]
日期:2025-11-20
卷期号:330 (1): H12-H30
标识
DOI:10.1152/ajpheart.00595.2025
摘要
Myeloid cells are known to contribute to the progression of myocardial infarction. However, the precise roles of these cells have not been fully elucidated. Single-cell RNA sequencing analysis demonstrated a population of glycoprotein A repetition-predominant (GARP)-expressing myeloid cells (GEM cells) that were derived from heart-resident fibrocytes. GEM cells were found to regulate neutrophil infiltration and cardiomyocyte apoptosis, resulting in detrimental cardiac remodeling. Spatial transcriptomics suggests that GEM cells are also present in human infarcted myocardium.
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