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载有 VEGF 的有指导意义的纳米纤维支架为血管生成和心脏修复创造了一个微环境。

Instructive nanofiber scaffolds with VEGF create a microenvironment for arteriogenesis and cardiac repair.

机构信息

Institute of Biomedical Sciences, Academia Sinica, Taipei 11574, Taiwan.

出版信息

Sci Transl Med. 2012 Aug 8;4(146):146ra109. doi: 10.1126/scitranslmed.3003841.

Abstract

Angiogenic therapy is a promising approach for tissue repair and regeneration. However, recent clinical trials with protein delivery or gene therapy to promote angiogenesis have failed to provide therapeutic effects. A key factor for achieving effective revascularization is the durability of the microvasculature and the formation of new arterial vessels. Accordingly, we carried out experiments to test whether intramyocardial injection of self-assembling peptide nanofibers (NFs) combined with vascular endothelial growth factor (VEGF) could create an intramyocardial microenvironment with prolonged VEGF release to improve post-infarct neovascularization in rats. Our data showed that when injected with NF, VEGF delivery was sustained within the myocardium for up to 14 days, and the side effects of systemic edema and proteinuria were significantly reduced to the same level as that of control. NF/VEGF injection significantly improved angiogenesis, arteriogenesis, and cardiac performance 28 days after myocardial infarction. NF/VEGF injection not only allowed controlled local delivery but also transformed the injected site into a favorable microenvironment that recruited endogenous myofibroblasts and helped achieve effective revascularization. The engineered vascular niche further attracted a new population of cardiomyocyte-like cells to home to the injected sites, suggesting cardiomyocyte regeneration. Follow-up studies in pigs also revealed healing benefits consistent with observations in rats. In summary, this study demonstrates a new strategy for cardiovascular repair with potential for future clinical translation.

摘要

血管生成治疗是一种有前途的组织修复和再生方法。然而,最近使用蛋白质输送或基因治疗来促进血管生成的临床试验未能提供治疗效果。实现有效再血管化的关键因素是微血管的耐久性和新动脉血管的形成。因此,我们进行了实验,以测试心肌内注射自组装肽纳米纤维(NFs)与血管内皮生长因子(VEGF)结合是否可以创建具有延长 VEGF 释放的心肌内微环境,以改善大鼠心肌梗死后的新血管生成。我们的数据表明,当注射 NF 时,VEGF 输送在心肌内持续长达 14 天,并且全身水肿和蛋白尿的副作用显著降低到与对照组相同的水平。NF/VEGF 注射可显著改善心肌梗死后 28 天的血管生成、动脉生成和心脏功能。NF/VEGF 注射不仅允许进行局部控制释放,还将注射部位转化为有利的微环境,募集内源性成肌纤维细胞,并有助于实现有效的再血管化。工程化的血管壁龛进一步吸引了新的心肌细胞样细胞群体归巢到注射部位,提示心肌细胞再生。在猪中的后续研究也揭示了与在大鼠中观察到的一致的愈合益处。总之,这项研究展示了一种具有未来临床转化潜力的心血管修复新策略。

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