医学
结扎
体内
心肌梗塞
成纤维细胞
缺血
梗塞
离体
病理
心脏病学
再灌注损伤
心脏缺血
动物模型
动脉
分布(数学)
邻近连接试验
心室重构
Pet成像
生物医学工程
受体
心功能曲线
阻塞(统计)
正电子发射断层摄影术
核医学
细胞
心肌缺血
作者
Gyu Seong Heo,Ying‐Hwey Nai,Jaume Ramon Otaegui,Steven Yang,Hannah Luehmann,Gengyang Yuan,David Onthank,Madeleine Ennis,Jeffrey S. Brown,Kory J. Lavine,Robert J. Gropler,Yongjian Liu
标识
DOI:10.2967/jnumed.125.270555
摘要
Fibroblast activation protein-expressing (FAP+) fibroblasts are central mediators of cardiac remodeling after injury or disease. The aim of this study was to evaluate a new PET tracer, 64Cu-LNTH-1363S, to detect FAP+ fibroblasts in myocardial infarction (MI) mouse models. Methods: The permanent left anterior descending coronary artery ligation and the echocardiography-guided ischemia reperfusion models were used to assess the targeting efficiency of 64Cu-LNTH-1363S. Competitive receptor blocking and autoradiography studies were performed to confirm the in vivo targeting specificity. Results: 64Cu-LNTH-1363S demonstrated sensitive and specific detection of FAP+ cells in the 2 MI models. Kinetic modeling data showed that the distribution volume was higher in the infarct zone than in the remote myocardium. Conclusion: This study establishes the feasibility of 64Cu-LNTH-1363S for noninvasive detection of FAP+ fibroblasts in MI mouse models and provides preclinical data to support further investigation of this process in humans after various forms of cardiac injury.
科研通智能强力驱动
Strongly Powered by AbleSci AI