Evidence map›Paper›PMID 37989085›Full record

ArticleCell reports methods2023

Third-generation rabies viral vectors allow nontoxic retrograde targeting of projection neurons with greatly increased efficiency.

Lei Jin, Heather A Sullivan, Mulangma Zhu, Nicholas E Lea, Thomas K Lavin, Xin Fu, Makoto Matsuyama, YuanYuan Hou, Guoping Feng, Ian R Wickersham

Open access · goldAbstract read
In one paragraph

Article in Cell reports methods, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Rabies virus-based barcoded neuroanatomy resolved by single-cell RNA andbioRxiv : the preprint server for biology · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Lei JinMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Heather A SullivanMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Mulangma ZhuMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Nicholas E LeaMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Thomas K LavinMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Xin FuMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA; Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.
Makoto MatsuyamaMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
YuanYuan HouMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Guoping FengMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA; Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Ian R WickershamMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA. Electronic address: wickersham@mit.edu.
McGovern Institute for Brain Research · USBroad Institute · US

Funding

Generation of novel cell type specific mouse genetic toolsU19MH114830 · NIMH · ALLEN INSTITUTE · PI NGAI, JOHN J. · 2017 to 2021
$64.7M
Anatomical characterization of neuronal cell types of the mouse brainU01MH114829 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ASCOLI, GIORGIO A, DONG, HONG-WEI · 2017 to 2021
$13.9M
Re-engineering Rabies VirusRF1MH120017 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WICKERSHAM, IAN R · 2019 to 2019
$2.6M
Novel technologies for nontoxic transsynaptic tracingU01MH106018 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WICKERSHAM, IAN R · 2014 to 2016
$2.5M
NIMH NIH HHS RF1 MH120017NIMH NIH HHS U01 MH106018NIMH NIH HHS U01 MH114829NIMH NIH HHS U19 MH114830
6 · The paper itself

Abstract

Rabies viral vectors have become important components of the systems neuroscience toolkit, allowing both direct retrograde targeting of projection neurons and monosynaptic tracing of inputs to defined postsynaptic populations, but the rapid cytotoxicity of first-generation (ΔG) vectors limits their use to short-term experiments. We recently introduced second-generation, double-deletion-mutant (ΔGL) rabies viral vectors, showing that they efficiently retrogradely infect projection neurons and express recombinases effectively but with little to no detectable toxicity; more recently, we have shown that ΔGL viruses can be used for monosynaptic tracing with far lower cytotoxicity than the first-generation system. Here, we introduce third-generation (ΔL) rabies viral vectors, which appear to be as nontoxic as second-generation ones but have the major advantage of growing to much higher titers, resulting in significantly increased numbers of retrogradely labeled neurons in vivo.

Indexed as

RabiesRabies virusGenetic VectorsHumansInterneuronsNeuronsCP: Neuroscience

Identifiers

PMID37989085
PMCPMC10694603
OpenAlexW4388821794

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.