Enhancer-AAVs allow genetic access to oligodendrocytes and diverse populations of astrocytes across species

Author:

Mich John K.ORCID,Sunil SmrithiORCID,Johansen NelsonORCID,Martinez Refugio A.ORCID,Leytze MckailaORCID,Gore Bryan B.ORCID,Mahoney Joseph T.ORCID,Ben-Simon YoavORCID,Bishaw YemeserachORCID,Brouner KrissyORCID,Campos JazminORCID,Canfield RyanORCID,Casper TamaraORCID,Dee NickORCID,Egdorf TomORCID,Gary AmandaORCID,Gibson ShaneORCID,Goldy JeffORCID,Groce Erin L.ORCID,Hirschstein DanielORCID,Loftus LukeORCID,Lusk NickORCID,Malone JocelinORCID,Martin Naomi X.ORCID,Monet DejaORCID,Omstead VictoriaORCID,Opitz-Araya XimenaORCID,Oster AaronORCID,Pom Christina A.ORCID,Potekhina LydiaORCID,Reding MelissaORCID,Rimorin ChristineORCID,Ruiz AugustinORCID,Sedeño-Cortés Adriana E.ORCID,Shapovalova Nadiya V.ORCID,Taormina MichaelORCID,Taskin NazORCID,Tieu MichaelORCID,Valera Cuevas Nasmil J.ORCID,Weed NatalieORCID,Way SharonORCID,Yao ZizhenORCID,McMillen Delissa A.ORCID,Kunst MichaelORCID,McGraw MedeaORCID,Thyagarajan BargaviORCID,Waters JackORCID,Bakken Trygve E.ORCID,Yao ShenqinORCID,Smith Kimberly A.ORCID,Svoboda KarelORCID,Podgorski KasparORCID,Kojima YoshikoORCID,Horwitz Greg D.ORCID,Zeng HongkuiORCID,Daigle Tanya L.ORCID,Lein Ed S.ORCID,Tasic BosiljkaORCID,Ting Jonathan T.ORCID,Levi Boaz P.ORCID

Abstract

AbstractProper brain function requires the assembly and function of diverse populations of neurons and glia. Single cell gene expression studies have mostly focused on characterization of neuronal cell diversity; however, recent studies have revealed substantial diversity of glial cells, particularly astrocytes. To better understand glial cell types and their roles in neurobiology, we built a new suite of adeno-associated viral (AAV)-based genetic tools to enable genetic access to astrocytes and oligodendrocytes. These oligodendrocyte and astrocyte enhancer-AAVs are highly specific (usually > 95% cell type specificity) with variable expression levels, and our astrocyte enhancer-AAVs show multiple distinct expression patterns reflecting the spatial distribution of astrocyte cell types. To provide the best glial-specific functional tools, several enhancer-AAVs were: optimized for higher expression levels, shown to be functional and specific in rat and macaque, shown to maintain specific activity in epilepsy where traditional promoters changed activity, and used to drive functional transgenes in astrocytes including Cre recombinase and acetylcholine-responsive sensor iAChSnFR. The astrocyte-specific iAChSnFR revealed a clear reward-dependent acetylcholine response in astrocytes of the nucleus accumbens during reinforcement learning. Together, this collection of glial enhancer-AAVs will enable characterization of astrocyte and oligodendrocyte populations and their roles across species, disease states, and behavioral epochs.

Publisher

Cold Spring Harbor Laboratory

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