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Biomimicking Fiber Scaffold as an Effective In Vitro and In Vivo MicroRNA Screening Platform for Directing Tissue Regeneration

机译:仿生纤维支架作为指导组织再生的有效体外和体内MicroRNA筛选平台

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摘要

MicroRNAs effectively modulate protein expression and cellular response. Unfortunately, the lack of robust nonviral delivery platforms has limited the therapeutic application of microRNAs. Additionally, there is a shortage of drug‐screening platforms that are directly translatable from in vitro to in vivo. Here, a fiber substrate that provides nonviral delivery of microRNAs for in vitro and in vivo microRNA screening is introduced. As a proof of concept, difficult‐to‐transfect primary neurons are targeted and the efficacy of this system is evaluated in a rat spinal cord injury model. With this platform, enhanced gene‐silencing is achieved in neurons as compared to conventional bolus delivery (p < 0.05). Thereafter, four well‐recognized microRNAs (miR‐21, miR‐222, miR‐132, and miR‐431) and their cocktails are screened systematically. Regardless of age and origin of the neurons, similar trends are observed. Next, this fiber substrate is translated into a 3D system for direct in vivo microRNA screening. Robust nerve ingrowth is observed as early as two weeks after scaffold implantation. Nerve regeneration in response to the microRNA cocktails is similar to in vitro experiments. Altogether, the potential of the fiber platform is demonstrated in providing effective microRNA screening and direct translation into in vivo applications.
机译:MicroRNA有效调节蛋白质表达和细胞反应。不幸的是,缺乏健壮的非病毒传递平台限制了microRNA的治疗应用。此外,缺乏可直接从体外转化为体内的药物筛选平台。在此,介绍了一种纤维底物,该纤维底物可提供非病毒的microRNA递送用于体外和体内microRNA筛选。作为概念的证明,靶向难以转染的原代神经元,并在大鼠脊髓损伤模型中评估了该系统的功效。与常规推注递送相比,使用该平台可增强神经元的基因沉默(p <0.05)。此后,系统地筛选了四个公认的microRNA(miR-21,miR-222,miR-132和miR-431)及其混合物。无论神经元的年龄和起源如何,都可以观察到类似的趋势。接下来,将该纤维基质转化为3D系统,以直接进行体内microRNA筛选。支架植入后两周即可观察到强健的神经向内生长。响应microRNA混合物的神经再生与体外实验相似。总而言之,光纤平台的潜力在提供有效的microRNA筛选和直接翻译到体内应用中得到了证明。

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