Login / Signup

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

John K MichSmrithi SunilNelson J JohansenRefugio A MartinezMckaila LeytzeBryan B GoreJoseph T MahoneyYoav Ben-SimonYemeserach BishawKrissy BrounerJazmin CamposRyan A CanfieldTamara CasperNick DeeTom EgdorfAmanda GaryShane GibsonJeff GoldyErin L GroceDaniel HirschsteinLuke V LoftusNicholas A LuskJocelin MaloneNaomi X MartinDeja MonetVictoria OmsteadXimena Opitz-ArayaAaron OsterChristina Alice PomLydia PotekhinaMelissa RedingChristine RimorinAugustin RuizAdriana Sedeño CortésNadiya V ShapovalovaMichael J TaorminaNaz TaskinMichael TieuNasmil Valera CuevasNatalie WeedSharon W WayZizhen YaoDelissa A McMillenMichael KunstMedea McGrawBargavi ThyagarajanJack WatersTrygve E BakkenShenqin YaoKimberly A SmithKarel SvobodaKaspar PodgorskiYoshiko KojimaGregory D HorwitzHongkui ZengTanya L DaigleEd S LeinBosiljka TasicJonathan T TingBoaz P Levi
Published in: bioRxiv : the preprint server for biology (2023)
Proper 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.
Keyphrases