Cell ReportsNeurosciencePeer-reviewed journal article
Enhancer AAVs for targeting spinal motor neurons and descending motor pathways in rodents and macaque
Emily KussickiD, Nelson JohanseniD, Naz TaskiniD, Ananya ChowdhuryiD, Meagan A. QuinlaniD, Alex FraseriD, Andrew G. Clark, Brooke WynaldaiD, Refugio A. MartineziD, Erin L GroceiD, Melissa RedingiD, Elizabeth LiangiD, Lyudmila ShulgaiD, Cindy Tzu-Ling HuangiD, Tamara CasperiD, Michael ClarkiD, Windy HoiD, Yuan GaoiD, Cindy T. J. van VelthoveniD, Cassandra SobieskiiD, Rebecca FerreriD, Melissa R. BergiD, Britni C CurtisiD, Christopher N. EnglishiD, Jesse C. Day, , Tanya L. DaigleiD
Abstract
Experimental access to cell types within the mammalian spinal cord is severely limited by the availability of genetic tools. To enable access to lower motor neurons (LMNs) and LMN subtypes, we generated single cell multiome datasets from mouse and macaque spinal cords and discovered putative enhancers for each neuronal population. We cloned these enhancers into adeno-associated viral vectors (AAVs) driving a reporter fluorophore and functionally screened them in mouse. We extensively characterized the most promising candidate enhancers in rat and macaque and developed an optimized pan LMN enhancer virus. Additionally, we generated derivative viruses expressing iCre297T recombinase or ChR2-EYFP for labeling and functional studies, and we created a single vector with combined enhancer elements to achieve simultaneous labeling of layer 5 extratelencephalic projecting (ET) neurons and LMNs. This unprecedented LMN toolkit will enable future investigations of cell type function across species and potential therapeutic interventions for human neurodegenerative diseases.
- organism: mouse
- organism: rat
- organism: non-human primate
- assay: scRNA-seq
- research focus: cell type annotation
- approach: experimental assay
- Citations
- 27
- FWCI
- 14.78
- Field percentile
- top 1%
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