We used kidney-targeted, non-viral, transposon-mediated gene delivery to express the mouse Slc3a1 transgene in one kidney of cystinuria type A (Slc3a1 (-/-)) mice. We found a 44% reduction in urinary cystine concentration at 154 days post-gene transfer, although there was no significant effect on cystine stone formation. Our results indicate that it is possible to achieve kidney-targeted gene transfer, resulting in reduction of cystine concentration in the urine of a cystinuria type A animal model. This proof of concept lays the foundation for future studies directed at gene therapy for cystinuria and other kidney diseases.
Partial correction of cystinuria type A in mice via kidney-targeted transposon delivery.
通过肾脏靶向转座子递送部分纠正小鼠 A 型胱氨酸尿症
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作者:Woodard Lauren E, Welch Richard C, Menshikh Anna, Luo Wentian, Williams Felisha M, Peek Jennifer L, Sha Feng, Veach Ruth Ann, Kaja Aparna, Beckerman Thomas M, Ikizler Talat Alp, Wilson Matthew H
| 期刊: | Molecular Therapy-Nucleic Acids | 影响因子: | 6.100 |
| 时间: | 2025 | 起止号: | 2025 Jul 21; 36(3):102639 |
| doi: | 10.1016/j.omtn.2025.102639 | ||
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