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Protein transduction therapy into cochleae via the round window niche in guinea pigs

机译:通过豚鼠的圆窗小生境将蛋白质转导到耳蜗中

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摘要

Cell-penetrating peptides (CPPs) are short sequences of amino acids that facilitate the penetration of conjugated cargoes across mammalian cell membranes, and as such, they may provide a safe and effective method for drug delivery to the inner ear. Simple polyarginine peptides have been shown to induce significantly higher cell penetration rates among CPPs. Herein, we show that a peptide consisting of nine arginines (“9R”) effectively delivered enhanced green fluorescent protein (EGFP) into guinea pig cochleae via the round window niche without causing any deterioration in auditory function. A second application, 24 hours after the first, prolonged the presence of EGFP. To assess the feasibility of protein transduction using 9R-CPPs via the round window, we used “X-linked inhibitor of apoptosis protein” (XIAP) bonded to a 9R peptide (XIAP-9R). XIAP-9R treatment prior to acoustic trauma significantly reduced putative hearing loss and the number of apoptotic hair cells loss in the cochleae. Thus, the topical application of molecules fused to 9R-CPPs may be a simple and promising strategy for treating inner ear diseases.
机译:细胞穿透肽(CPPs)是氨基酸的短序列,可促进缀合的货物穿过哺乳动物细胞膜的穿透,因此,它们可以为将药物递送到内耳提供安全有效的方法。简单的聚精氨酸肽已显示出可诱导CPP之间明显更高的细胞渗透率。本文中,我们显示了由九个精氨酸(“ 9R”)组成的肽通过圆形窗口位有效地将增强的绿色荧光蛋白(EGFP)递送至豚鼠耳蜗,而不会引起听觉功能的任何恶化。第一次施用后24小时进行第二次施用可延长EGFP的存在时间。为了评估通过圆窗使用9R-CPPs进行蛋白转导的可行性,我们使用了与9R肽(XIAP-9R)结合的“ X连锁凋亡蛋白抑制剂”(XIAP)。在听觉创伤之前进行XIAP-9R治疗可显着降低假定的听力损失和耳蜗中凋亡性毛细胞的损失数量。因此,与9R-CPPs融合的分子的局部应用可能是治疗内耳疾病的简单而有前途的策略。

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