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载 miRNA 泡泡脂质体经系统给药治疗后肢缺血症中的 miR-126。

Systemic delivery of miR-126 by miRNA-loaded Bubble liposomes for the treatment of hindlimb ischemia.

机构信息

Department of Drug Delivery and Molecular Biopharmaceutics, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.

Laboratory of Drug and Gene Delivery Research, Faculty of Pharma-Sciences, Teikyo University, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan.

出版信息

Sci Rep. 2014 Jan 24;4:3883. doi: 10.1038/srep03883.

Abstract

Currently, micro RNA (miRNA) is considered an attractive target for therapeutic intervention. A significant obstacle to the miRNA-based treatments is the efficient delivery of miRNA to the target tissue. We have developed polyethylene glycol-modified liposomes (Bubble liposomes (BLs)) that entrap ultrasound (US) contrast gas and can serve as both plasmid DNA (pDNA) or small interfering RNA (siRNA) carriers and US contrast agents. In this study, we investigated the usability of miRNA-loaded BLs (mi-BLs) using a hindlimb ischemia model and miR-126. It has been reported that miR-126 promotes angiogenesis via the inhibition of negative regulators of VEGF signaling. We demonstrated that mi-BLs could be detected using diagnostic US and that mi-BLs with therapeutic US could deliver miR-126 to an ischemic hindlimb, leading to the induction of angiogenic factors and the improvement of blood flow. These results suggest that combining mi-BLs with US may be useful for US imaging and miRNA delivery.

摘要

目前,微 RNA(miRNA)被认为是治疗干预的一个有吸引力的靶点。miRNA 治疗的一个显著障碍是将 miRNA 高效递送到靶组织。我们已经开发了聚乙二醇修饰的脂质体(Bubble 脂质体(BLs)),其包埋超声(US)对比气体,并可作为质粒 DNA(pDNA)或小干扰 RNA(siRNA)载体和 US 对比剂。在这项研究中,我们使用后肢缺血模型和 miR-126 研究了负载 miRNA 的 BL(mi-BL)的可用性。据报道,miR-126 通过抑制 VEGF 信号通路的负调节剂促进血管生成。我们证明,mi-BL 可以使用诊断性 US 检测到,并且具有治疗性 US 的 mi-BL 可以将 miR-126 递送到缺血性后肢,从而诱导血管生成因子并改善血流。这些结果表明,将 mi-BL 与 US 结合使用可能有助于 US 成像和 miRNA 递送。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c56f/3900923/e6e7f424b7df/srep03883-f1.jpg

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