医学
自噬
基因敲除
基因剔除小鼠
细胞生物学
炎症
机制(生物学)
跨膜蛋白
程序性细胞死亡
泛素
疾病
神经科学
细胞
生物信息学
细胞损伤
融合蛋白
下调和上调
限制
癌症研究
再灌注损伤
功能(生物学)
心功能曲线
表型
恶化
体内
血运重建
促进
心肌细胞
信号转导
死因
缺血
转基因小鼠
作者
Siyi Zhou,Jiayi Liu,Manli Hu,Song Tian,Junjie Zhou,Wei Li,Hailian Chen,Maoji Yin,Shiyi Wang,Lei Luo,Long Zhang,Xiangqiang Zhou,Xu Cheng,Quanqing Qiu,Jinsheng Wang,Weiyi Qu,Yufeng Hu,Péter Ferdinandy,Mario Chiong,Mayarling F. Troncoso
出处
期刊:Circulation
[Lippincott Williams & Wilkins]
日期:2026-08-04
标识
DOI:10.1161/circulationaha.125.077971
摘要
BACKGROUND: Myocardial ischemia-reperfusion (MIR) injury compromises therapeutic effects of revascularization and leads to functional impairment and exacerbation of structural damage in the heart. Limiting the damage caused by MIR is crucial but is still an unmet clinical need because of the complexity of the underlying mechanisms. Increasing evidence suggests that lysosomal autophagy plays a significant regulatory role in MIR injury. The specific mechanisms involved remain to be fully understood. METHODS: We here systematically analyzed the murine MIR model database to screen the potentially protective lysosome-localized proteins against MIR injury. The positive hits were further functionally screened and validated for their capability on autophagy and hypoxia/reoxygenation insults of cardiomyocytes. After exploring the detailed molecular mechanism underlying the protective effects of the target protein, we generated target gene cardiac-specific knockout mice and overexpression mice to verify its function in mouse MIR injury models. RESULTS: LAPTM4A (lysosome-associated protein transmembrane 4 alpha) stood out as a significant protective lysosome-localized protein from the screening. LAPTM4A deficiency significantly heightened the inflammatory response and cell death both in primary cardiomyocytes and in a MIR-induced mouse model. Conversely, LAPTM4A overexpression exerted protective effects on cell viability and myocardial damage. Mechanistically, LAPTM4A interacts with Rubicon (Run domain Beclin1-interacting and cysteine-rich domain-containing protein), hindering its engagement within the Beclin1 complex, resulting in a robust augmentation of autophagic flux and thereby mitigating cardiac damage during reperfusion. It is important to note that Rubicon knockdown markedly reversed the aggravated injury induced by LAPTM4A knockdown, further verifying the effects of LAPTM4A depend on Rubicon. CONCLUSIONS: Our findings screened out and validated that LAPTM4A is a lysosome-localized protein exerting protective effects against MIR injury by facilitating autophagic flux. Targeting LAPTM4A represents a promising therapeutic strategy for mitigating MIR injury.
科研通智能强力驱动
Strongly Powered by AbleSci AI