Protein transduction into the mouse otocyst using arginine-rich cell-penetrating peptides

被引:12
|
作者
Miwa, Toru [1 ]
Minoda, Ryosei [1 ]
Kaitsuka, Taku [2 ]
Ise, Momoko [1 ]
Tomizawa, Kazuhito [2 ]
Yumoto, Eiji [1 ]
机构
[1] Kumamoto Univ, Grad Sch Med, Dept Otolaryngol Head & Neck Surg, Kumamoto 8600811, Japan
[2] Kumamoto Univ, Fac Life Sci, Dept Mol Physiol, Kumamoto 8600811, Japan
关键词
cell-penetrating peptides; otocyst; poly-arginine; protein transduction; HUMAN IMMUNODEFICIENCY VIRUS; TRANSLOCATION MECHANISMS; GENE-TRANSFER; INNER-EAR; DELIVERY; TERMINUS; DOMAINS; COCHLEA; SYSTEM; CANCER;
D O I
10.1097/WNR.0b013e32834da8f8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The mouse otocyst, an anlage of the inner ear, is an attractive experimental target for developing treatment modalities for congenital inner ear diseases and for studying inner ear development. Poly-arginine (6-12 residues) is a cell-penetrating peptide and can be used to deliver cargo into cells. Here, we achieved transutero delivery of enhanced green fluorescent protein (EGFP) fused to a nine-arginine peptide into mouse embryonic otocysts. The EGFP signal was detected both in the lining cells of the otocysts and in their vicinity at 18 h post injection. Mice injected with EGFP fused to a nine-arginine peptide had normal auditory and vestibular functions. These data suggest that protein transduction using poly-arginine may be a useful alternative strategy to commonly used gene delivery methods for delivering therapeutically relevant molecules to the developing inner ear. NeuroReport 22:994-999 (C) 2011 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:994 / 999
页数:6
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