A Novel Adeno-Associated Viral Variant for Efficient and Selective Intravitreal Transduction of Rat Muller Cells

被引:145
作者
Klimczak, Ryan R.
Koerber, James T.
Dalkara, Deniz
Flannery, John G.
Schaffer, David V.
机构
[1] Department of Molecular and Cellular Biology, University of California, Berkeley, CA
[2] Department of Chemical Engineering, Department of Bioengineering, The University of California, Berkeley, CA
[3] Helen Wills Neuroscience Institute, University of California, Berkeley, CA
来源
PLOS ONE | 2009年 / 4卷 / 10期
关键词
RETINAL-DETACHMENT; VISUAL FUNCTION; GENE-TRANSFER; VIRUS; VECTOR; THERAPY; ASTROCYTES; TROPISM; BINDING; VISION;
D O I
10.1371/journal.pone.0007467
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The pathologies of numerous retinal degenerative diseases can be attributed to a multitude of genetic factors, and individualized treatment options for afflicted patients are limited and cost-inefficient. In light of the shared neurodegenerative phenotype among these disorders, a safe and broad-based neuroprotective approach would be desirable to overcome these obstacles. As a result, gene delivery of secretable-neuroprotective factors to Muller cells, a type of retinal glia that contacts all classes of retinal neurons, represents an ideal approach to mediate protection of the entire retina through a simple and innocuous intraocular, or intravitreal, injection of an efficient vehicle such as an adeno-associated viral vector (AAV). Although several naturally occurring AAV variants have been isolated with a variety of tropisms, or cellular specificities, these vectors inefficiently infect Muller cells via intravitreal injection. Methodology/Principal Findings: We have previously applied directed evolution to create several novel AAV variants capable of efficient infection of both rat and human astrocytes through iterative selection of a panel of highly diverse AAV libraries. Here, in vivo and in vitro characterization of these isolated variants identifies a previously unreported AAV variant ShH10, closely related to AAV serotype 6 (AAV6), capable of efficient, selective Muller cell infection through intravitreal injection. Importantly, this new variant shows significantly improved transduction relative to AAV2 (>60%) and AAV6. Conclusions/Significance: Our findings demonstrate that AAV is a highly versatile vector capable of powerful shifts in tropism from minor sequence changes. This isolated variant represents a new therapeutic vector to treat retinal degenerative diseases through secretion of neuroprotective factors from Muller cells as well as provides new opportunities to study their biological functions in the retina.
引用
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页数:10
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