Transduction and Genome Editing of the Heart with Adeno-Associated Viral Vectors Loaded onto Electrospun Polydioxanone Nonwoven Fabrics

被引:2
作者
Furuno, Kotoko [1 ]
Suzuki, Keiichiro [1 ,2 ,3 ]
Sakai, Shinji [1 ]
机构
[1] Osaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, 1-3 Machikaneyama Cho, Toyonaka 5608531, Japan
[2] Osaka Univ, Inst Adv Cocreat Studies, 1-3 Machikaneyama Cho, Toyonaka 5608531, Japan
[3] Osaka Univ, Grad Sch Frontier Biosci, 1-3 Yamadaoka, Suita 5650871, Japan
基金
日本学术振兴会;
关键词
polydioxanone; electrospinning; gene delivery; genome editing; electrospun nonwoven fabrics; HYDROLYTIC DEGRADATION; GENE DELIVERY; IMPROVES; THERAPY; RELEASE;
D O I
10.3390/biom14040506
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we introduce electrospun polydioxanone (PDO) nonwoven fabrics as a platform for the delivery of adeno-associated virus (AAV) vectors for transduction and genome editing by adhering them to organ surfaces, including the heart. AAV vectors were loaded onto the PDO fabrics by soaking the fabrics in a solution containing AAV vectors. In vitro, the amount of AAV vectors loaded onto the fabrics could be adjusted by changing their concentration in the solution, and the number of cells expressing the green fluorescent protein (GFP) encoded by the AAV vectors increased in correlation with the increasing amount of loaded AAV vectors. In vivo, both transduction and genome editing resulted in the observation of GFP expression around AAV vector-loaded PDO fabrics attached to the surfaces of mouse hearts, indicating effective transduction and expression at the target site. These results demonstrate the great potential of electrospun PDO nonwoven fabrics carrying therapeutic AAV vectors for gene therapy.
引用
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页数:12
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