TFEB-mediated activation of the lysosome-autophagy system affects the transduction efficiency of adeno-associated virus 2

被引:7
作者
Popp, Lauren [1 ]
Gomez, Eric [2 ]
Orji, Whitney [2 ]
Ho, Michelle [2 ]
Suh, Junghae [2 ,3 ,4 ]
Segatori, Laura [1 ,2 ,3 ,4 ]
机构
[1] Rice Univ, Dept Chem & Biomol Engn, 6100 Main St,MS 362, Houston, TX 77005 USA
[2] Rice Univ, Dept Bioengn, 6500 Main St,Suite 1030, Houston, TX USA
[3] Rice Univ, Dept Biosci, 6100 Main St,MS 140, Houston, TX 77005 USA
[4] Rice Univ, Syst Synthet & Phys Biol Program, 6100 Main St,MS 180, Houston, TX 77005 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Adeno-associated virus; Autophagy; Lysosome; Transcription factor EB; CELLULAR CLEARANCE; GENE-THERAPY; IN-VITRO; INFECTION; VECTORS; PATHWAY; LC3; REPLICATION; BIOGENESIS; IMMUNITY;
D O I
10.1016/j.virol.2017.06.030
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Adeno-associated virus (AAV)-mediated gene transfer is an appealing therapeutic option due to AAV's safety profile. Effective delivery of AAV's genetic cargo to the nucleus, however, requires evasion of host cell barriers, including cellular clearance mechanisms mediated by the lysosome-autophagy system. We used AAV serotype 2 to monitor the autophagic response to cellular internalization of AAV and to characterize the effect of AAV-induced activation of autophagy on transgene expression. We found AAV2 internalization to induce activation of transcription factor EB, a master regulator of autophagy and lysosomal biogenesis, and upregulation of the lysosome-autophagy system. We showed that AAV2-induced activation of autophagy parallels a reduction in transgene expression, but also an increase in autophagic clearance of protein aggregates. These results can inform the design of AAV vectors with autophagy-modulating properties for applications ranging from the design of efficient gene delivery vectors to the treatment of diseases characterized by accumulation of autophagic cargo.
引用
收藏
页码:1 / 8
页数:8
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