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

John K Mich, Smrithi Sunil, Nelson Johansen, Refugio A Martinez, Jiatai Liu, Bryan B Gore, Joseph T Mahoney, Mckaila Leytze, Yoav Ben-Simon, Darren Bertagnolli, Ravi Bhowmik, Yemeserach Bishaw, Krissy Brouner, Jazmin Campos, Ryan Canfield, Tamara Casper, Nicholas P Donadio, Nadezhda I Dotson, Tom Egdorf, Amanda Gary, Shane Gibson, Jeff Goldy, Erin L Groce, Kenta M Hagihara, Daniel Hirschstein, Han Hou, Will D Laird, Elizabeth Liang, Luke Loftus, Nicholas Lusk, Jocelin Malone, Naomi X Martin, Deja Monet, Josh S Nagra, Dakota Newman, Nhan-Kiet Ngo, Paul A Olsen, Victoria Omstead, Ximena Opitz-Araya, Aaron Oster, Christina Alice Pom, Lydia Potekhina, Melissa Reding, Christine Rimorin, Augustin Ruiz, Adriana E Sedeno-Cortes, Nadiya V Shapovalova, Michael Taormina, Naz Taskin, Michael Tieu, Nasmil J Valera Cuevas, Sharon W Way, Natalie Weed, Vonn Wright, Zizhen Yao, Thomas Zhou, Delissa A McMillen, Michael Kunst, Medea McGraw, Bargavi Thyagarajan, Jack Waters, Trygve Bakken, Nick Dee, Shenqin Yao, Kimberly A Smith, Karel Svoboda, Kaspar Podgorski, Yoshiko Kojima, Gregory D Horwitz, Hongkui Zeng, Tanya L Daigle, Ed S Lein, Bosiljka Tasic, Jonathan T Ting, Boaz P Levi
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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 also 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 the 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 across transgenes and 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.

增强型AAVs允许遗传途径进入不同物种的少突胶质细胞和不同群体的星形胶质细胞。
正确的大脑功能需要不同群体的神经元和神经胶质的组装和功能。单细胞基因表达研究主要集中在神经元细胞多样性的表征上;然而,最近的研究揭示了胶质细胞,特别是星形胶质细胞的多样性。为了更好地了解神经胶质细胞类型及其在神经生物学中的作用,我们建立了一套新的基于腺相关病毒(AAV)的遗传工具,以使星形胶质细胞和少突胶质细胞能够进行遗传访问。这些少突胶质细胞和星形胶质细胞增强子AAVs具有高度特异性(通常>95%的细胞类型特异性),表达水平可变,我们的星形胶质细胞增强因子AAVs显示出多种不同的表达模式,反映了星形胶质细胞类型的空间分布。为了提供最佳的神经胶质特异性功能工具,对几种增强子AAV进行了优化,以获得更高的表达水平,在大鼠和猕猴中显示出功能性和特异性,在传统启动子改变活性的癫痫中显示出维持特异性活性,并用于驱动星形胶质细胞中的功能性转基因,包括Cre重组酶和乙酰胆碱反应传感器iAChSnFR。星形胶质细胞特异性iAChSnFR揭示了伏隔核星形胶质细胞在强化学习过程中明显的奖赏依赖性乙酰胆碱反应。总之,这组胶质增强剂AAVs将能够表征星形胶质细胞和少突胶质细胞群体及其在物种、疾病状态和行为时代中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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