Evidence map›Paper›PMID 37873336›Full record

ArticlebioRxiv : the preprint server for biology2023

Cell specific single viral vector CRISPR/Cas9 editing and genetically encoded tool delivery in the central and peripheral nervous systems.

Jamie C Moffa, India N Bland, Jessica R Tooley, Vani Kalyanaraman, Monique Heitmeier, Meaghan C Creed, Bryan A Copits

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Jamie C MoffaWashington University Pain Center, Department of Anesthesiology, Washington University School of Medicine; St. Louis, MO.
India N BlandWashington University Pain Center, Department of Anesthesiology, Washington University School of Medicine; St. Louis, MO.
Jessica R TooleyWashington University Pain Center, Department of Anesthesiology, Washington University School of Medicine; St. Louis, MO.
Vani KalyanaramanWashington University Pain Center, Department of Anesthesiology, Washington University School of Medicine; St. Louis, MO.
Monique HeitmeierWashington University Pain Center, Department of Anesthesiology, Washington University School of Medicine; St. Louis, MO.
Meaghan C CreedWashington University Pain Center, Department of Anesthesiology, Washington University School of Medicine; St. Louis, MO.
Bryan A CopitsWashington University Pain Center, Department of Anesthesiology, Washington University School of Medicine; St. Louis, MO.
Washington University in St. Louis · US

Funding

Ventral pallidal transcriptional adaptations underlying punishment-resistant opioid intakeR01DA056829 · NIDA · WASHINGTON UNIVERSITY · PI Meaghan C Creed, Vijay K Samineni · 2023 to 2026
$3.2M
Dissecting ventral pallidal plasticity in punishment-resistant opioid self-administrationR01DA058755 · NIDA · WASHINGTON UNIVERSITY · PI Meaghan C Creed · 2023 to 2026
$2.5M
Dissecting the role of ventral pallidal projections to nucleus accumbens in reward processingR01DA049924 · NIDA · WASHINGTON UNIVERSITY · PI CREED, MEAGHAN C · 2020 to 2024
$2.0M
Synaptic mechanisms of somatosensory circuit assemblyR01NS130046 · NINDS · WASHINGTON UNIVERSITY · PI Bryan Copits · 2023 to 2026
$2.0M
BRAIN Viral Vector Services and Distribution CoreU24NS124025 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RITOLA, KIMBERLY · 2021 to 2025
$1.9M
NIDA NIH HHS R01 DA049924NIDA NIH HHS R01 DA058755NINDS NIH HHS R01 NS130046NINDS NIH HHS U24 NS124025
6 · The paper itself

Abstract

Gene manipulation strategies using germline knockout, conditional knockout, and more recently CRISPR/Cas9 are crucial tools for advancing our understanding of the nervous system. However, traditional gene knockout approaches can be costly and time consuming, may lack cell-type specificity, and can induce germline recombination. Viral gene editing presents and an exciting alternative to more rapidly study genes of unknown function; however, current strategies to also manipulate or visualize edited cells are challenging due to the large size of Cas9 proteins and the limited packaging capacity of adeno-associated viruses (AAVs). To overcome these constraints, we have developed an alternative gene editing strategy using a single AAV vector and mouse lines that express Cre-dependent Cas9 to achieve efficient cell-type specific editing across the nervous system. Expressing Cre-dependent Cas9 in specific cell types in transgenic mouse lines affords more space to package guide RNAs for gene editing together with Cre-dependent, genetically encoded tools to manipulate, map, or monitor neurons using a single virus. We validated this strategy with three commonly used tools in neuroscience: ChRonos, a channelrhodopsin, for manipulating synaptic transmission using optogenetics; GCaMP8f for recording Ca2+ transients using fiber photometry, and mCherry for anatomical tracing of axonal projections. We tested these tools in multiple brain regions and cell types, including GABAergic neurons in the nucleus accumbens (NAc), glutamatergic neurons projecting from the ventral pallidum (VP) to the lateral habenula (LHb), dopaminergic neurons in the ventral tegmental area (VTA), and parvalbumin (PV)-positive proprioceptive neurons in the periphery. This flexible approach should be useful to identify novel genes that affect synaptic transmission, circuit activity, or morphology with a single viral injection.

Identifiers

PMID37873336
PMCPMC10592710
OpenAlexW4387536505

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.