Skip to main content

This is a preprint.

It has not yet been peer reviewed by a journal.

The National Library of Medicine is running a pilot to include preprints that result from research funded by NIH in PMC and PubMed.

bioRxiv logoLink to bioRxiv
[Preprint]. 2023 Sep 21:2023.09.20.558718. [Version 1] doi: 10.1101/2023.09.20.558718

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

John K Mich, Smrithi Sunil, Nelson Johansen, Refugio A Martinez, Mckaila Leytze, Bryan B Gore, Joseph T Mahoney, Yoav Ben-Simon, Yemeserach Bishaw, Krissy Brouner, Jazmin Campos, Ryan Canfield, Tamara Casper, Nick Dee, Tom Egdorf, Amanda Gary, Shane Gibson, Jeff Goldy, Erin L Groce, Daniel Hirschstein, Luke Loftus, Nick Lusk, Jocelin Malone, Naomi X Martin, Deja Monet, Victoria Omstead, Ximena Opitz-Araya, Aaron Oster, Christina A Pom, Lydia Potekhina, Melissa Reding, Christine Rimorin, Augustin Ruiz, Adriana E Sedeño-Cortés, Nadiya V Shapovalova, Michael Taormina, Naz Taskin, Michael Tieu, Nasmil J Valera Cuevas, Natalie Weed, Sharon Way, Zizhen Yao, Delissa A McMillen, Michael Kunst, Medea McGraw, Bargavi Thyagarajan, Jack Waters, Trygve E Bakken, Shenqin Yao, Kimberly A Smith, Karel Svoboda, Kaspar Podgorski, Yoshiko Kojima, Greg D Horwitz, Hongkui Zeng, Tanya L Daigle, Ed S Lein, Bosiljka Tasic, Jonathan T Ting, Boaz P Levi
PMCID: PMC10542530  PMID: 37790503

Abstract

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.

Full Text Availability

The license terms selected by the author(s) for this preprint version do not permit archiving in PMC. The full text is available from the preprint server.


Articles from bioRxiv are provided here courtesy of Cold Spring Harbor Laboratory Preprints

RESOURCES