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超声响应性治疗平台,用于即时监测和提高 tPA 抵抗型血栓的溶栓效率。

Ultrasound-responsive theranostic platform for the timely monitoring and efficient thrombolysis in thrombi of tPA resistance.

机构信息

Department of Cell Biology, Third Military Medical University, Chongqing, China.

School of Medicine, Chongqing University, Chongqing, China.

出版信息

Nat Commun. 2024 Aug 4;15(1):6610. doi: 10.1038/s41467-024-50741-y.

Abstract

There is no effective and noninvasive solution for thrombolysis because the mechanism by which certain thrombi become tissue plasminogen activator (tPA)-resistant remains obscure. Endovascular thrombectomy is the last option for these tPA-resistant thrombi, thus a new noninvasive strategy is urgently needed. Through an examination of thrombi retrieved from stroke patients, we found that neutrophil extracellular traps (NETs), ε-(γ-glutamyl) lysine isopeptide bonds and fibrin scaffolds jointly comprise the key chain in tPA resistance. A theranostic platform is designed to combine sonodynamic and mechanical thrombolysis under the guidance of ultrasonic imaging. Breakdown of the key chain leads to a recanalization rate of more than 90% in male rat tPA-resistant occlusion model. Vascular reconstruction is observed one month after recanalization, during which there was no thrombosis recurrence. The system also demonstrates noninvasive theranostic capabilities in managing pigs' long thrombi (>8 mm) and in revascularizing thrombosis-susceptible tissue-engineered vascular grafts, indicating its potential for clinical application. Overall, this noninvasive theranostic platform provides a new strategy for treating tPA-resistant thrombi.

摘要

由于某些血栓形成变得对组织型纤溶酶原激活剂(tPA)具有抗性的机制仍不清楚,因此目前尚无有效的非侵入性溶栓解决方案。对于这些 tPA 抗性血栓,血管内血栓切除术是最后的选择,因此迫切需要一种新的非侵入性策略。通过对从中风患者中取出的血栓进行检查,我们发现中性粒细胞胞外陷阱(NETs)、ε-(γ-谷氨酰)赖氨酸异肽键和纤维蛋白支架共同构成了 tPA 抗性的关键链。设计了一种治疗诊断平台,以在超声成像的指导下结合声动力学和机械溶栓。关键链的破坏导致雄性大鼠 tPA 抗性闭塞模型的再通率超过 90%。再通后一个月观察到血管重建,在此期间没有血栓复发。该系统还在处理猪的长血栓(>8mm)和再通易血栓形成的组织工程血管移植物方面展示了非侵入性治疗诊断能力,表明其具有临床应用的潜力。总体而言,这种非侵入性治疗诊断平台为治疗 tPA 抗性血栓提供了一种新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc1a/11298549/58ddbe2909cd/41467_2024_50741_Fig1_HTML.jpg

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