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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
来源:
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.
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页码:994 / 999
页数:6
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