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MSCs 仿生超声相变型纳米颗粒促进急性心肌梗死后的心脏功能恢复。

MSCs biomimetic ultrasonic phase change nanoparticles promotes cardiac functional recovery after acute myocardial infarction.

机构信息

Department of Ultrasound, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China; Ultrasound Molecular Imaging Joint Laboratory of Heilongjiang Province (International Cooperation), Harbin, 150086, China; Key Laboratories of Myocardial Ischemia, Harbin Medical University, Ministry of Education, Harbin, 150086, China.

Laboratory Animal Center, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.

出版信息

Biomaterials. 2025 Feb;313:122775. doi: 10.1016/j.biomaterials.2024.122775. Epub 2024 Aug 26.

Abstract

Acute Myocardial Infarction (AMI) has seen rising cases, particularly in younger people, leading to public health concerns. Standard treatments, like coronary artery recanalization, often don't fully repair the heart's microvasculature, risking heart failure. Advances show that Mesenchymal Stromal Cells (MSCs) transplantation improves cardiac function after AMI, but the harsh microenvironment post-AMI impacts cell survival and therapeutic results. MSCs aid heart repair via their membrane proteins and paracrine extracellular vesicles that carry microRNA-125b, which regulates multiple targets, preventing cardiomyocyte death, limiting fibroblast growth, and combating myocardial remodeling after AMI. This study introduces ultrasound-responsive phase-change bionic nanoparticles, leveraging MSCs' natural properties. These particles contain MSC membrane and microRNA-125b, with added macrophage membrane for stability. Using Ultrasound Targeted Microbubble Destruction (UTMD), this method targets the delivery of MSC membrane proteins and microRNA-125b to AMI's inflamed areas. This aims to enhance cardiac function recovery and provide precise, targeted AMI therapy.

摘要

急性心肌梗死(AMI)的病例不断增加,尤其是在年轻人中,引起了公众健康的关注。标准治疗方法,如冠状动脉再通,往往不能完全修复心脏的微血管,从而增加心力衰竭的风险。研究进展表明,间充质基质细胞(MSCs)移植可以改善 AMI 后的心脏功能,但 AMI 后恶劣的微环境会影响细胞的存活和治疗效果。MSCs 通过其膜蛋白和旁分泌的外泌体携带 microRNA-125b 来帮助心脏修复,microRNA-125b 可以调节多个靶标,防止心肌细胞死亡、限制成纤维细胞生长,并在 AMI 后对抗心肌重构。本研究引入了超声响应的相变仿生纳米粒子,利用了 MSCs 的天然特性。这些粒子包含 MSC 膜和 microRNA-125b,外加巨噬细胞膜以增加稳定性。通过超声靶向微泡破坏(UTMD),该方法将 MSC 膜蛋白和 microRNA-125b 靶向输送到 AMI 的炎症区域。目的是增强心脏功能的恢复,并提供精确、靶向的 AMI 治疗。

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