A toolbox of astrocyte-specific, serotype-independent adeno-associated viral vectors using microRNA targeting sequences

Amy J. Gleichman, Riki Kawaguchi, Michael V. Sofroniew and S. Thomas Carmichael ()
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Amy J. Gleichman: David Geffen School of Medicine at University of California—Los Angeles
Riki Kawaguchi: University of California Los Angeles
Michael V. Sofroniew: University of California—Los Angeles
S. Thomas Carmichael: David Geffen School of Medicine at University of California—Los Angeles

Nature Communications, 2023, vol. 14, issue 1, 1-18

Abstract: Abstract Astrocytes, one of the most prevalent cell types in the central nervous system (CNS), are critically involved in neural function. Genetically manipulating astrocytes is an essential tool in understanding and affecting their roles. Adeno-associated viruses (AAVs) enable rapid genetic manipulation; however, astrocyte specificity of AAVs can be limited, with high off-target expression in neurons and sparsely in endothelial cells. Here, we report the development of a cassette of four copies of six miRNA targeting sequences (4x6T) which triggers transgene degradation specifically in neurons and endothelial cells. In combination with the GfaABC1D promoter, 4x6T increases astrocytic specificity of Cre with a viral reporter from 99% in multiple serotypes in mice, and confers astrocyte specificity in multiple recombinases and reporters. We also present empty vectors to add 4x6T to other cargo, independently and in Cre/Dre-dependent forms. This toolbox of AAVs allows rapid manipulation of astrocytes throughout the CNS, is compatible with different AAV serotypes, and demonstrates the efficacy of using multiplexed miRNA targeting sequences to decrease expression in multiple off-target cell populations simultaneously.

Date: 2023
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DOI: 10.1038/s41467-023-42746-w

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