Evidence map›Paper›PMID 30341180›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2018

Global Connectivity and Function of Descending Spinal Input Revealed by 3D Microscopy and Retrograde Transduction.

Zimei Wang, Brian Maunze, Yunfang Wang, Pantelis Tsoulfas, Murray G Blackmore

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

61 citing papers in PubMed, 92 citations in OpenAlex.

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  15. Single-Nuclei Sequencing Reveals a Robust Corticospinal Response to Nearby Axotomy But Overall Insensitivity to Spinal Injury.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  16. Nonresolving Neuroinflammation Regulates Axon Regeneration in Chronic Spinal Cord Injury.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  17. Article
  18. Review
  19. Injury distance limits the transcriptional response to spinal injury.bioRxiv : the preprint server for biology · 2024
    Article
  20. Article

1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Zimei WangDepartment of Biomedical Sciences, Marquette University, Milwaukee, Wisconsin 53211, and.
Brian MaunzeDepartment of Biomedical Sciences, Marquette University, Milwaukee, Wisconsin 53211, and.
Yunfang WangDepartment of Neurological Surgery, Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Miami, Florida 33136.
Pantelis TsoulfasDepartment of Neurological Surgery, Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Miami, Florida 33136 murray.blackmore@marquette.edu ptsoulfa@med.miami.edu.ORCID 0000-0003-1974-6366
Murray G BlackmoreDepartment of Biomedical Sciences, Marquette University, Milwaukee, Wisconsin 53211, and murray.blackmore@marquette.edu ptsoulfa@med.miami.edu.
Marquette University · USUniversity of Miami · US

Funding

Functional Testing of KLF7 in Spinal Cord Injury: An Optogenetic ApproachR01NS083983 · NINDS · MARQUETTE UNIVERSITY · PI BLACKMORE, MURRAY G · 2013 to 2023
$3.5M
Strategies to maximize the functional benefit of regenerated corticospinal tract axonsR01NS107807 · NINDS · MARQUETTE UNIVERSITY · PI BLACKMORE, MURRAY G · 2018 to 2022
$1.7M
NINDS NIH HHS R01 NS083983NINDS NIH HHS R01 NS107807
6 · The paper itself

Abstract

The brain communicates with the spinal cord through numerous axon tracts that arise from discrete nuclei, transmit distinct functions, and often collateralize to facilitate the coordination of descending commands. This complexity presents a major challenge to interpreting functional outcomes from therapies that target supraspinal connectivity after injury or disease, while the wide distribution of supraspinal nuclei complicates the delivery of therapeutics. Here we harness retrograde viral vectors to overcome these challenges. We demonstrate that injection of AAV2-Retro to the cervical spinal cord of adult female mice results in highly efficient transduction of supraspinal populations throughout the brainstem, midbrain, and cortex. Some supraspinal populations, including corticospinal and rubrospinal neurons, were transduced with >90% efficiency, with robust transgene expression within 3 d of injection. In contrast, propriospinal and raphe spinal neurons showed much lower rates of retrograde transduction. Using tissue clearing and light-sheet microscopy we present detailed visualizations of descending axons tracts and create a mesoscopic projectome for the spinal cord. Moreover, chemogenetic silencing of supraspinal neurons with retrograde vectors resulted in complete and reversible forelimb paralysis, illustrating effective modulation of supraspinal function. Retrograde vectors were also highly efficient when injected after spinal injury, highlighting therapeutic potential. These data provide a global view of supraspinal connectivity and illustrate the potential of retrograde vectors to parse the functional contributions of supraspinal inputs.

Indexed as

AnimalsBrainBrain ChemistryFemaleImaging, Three-DimensionalMiceMice, Inbred C57BLNerve NetProprioceptionPyramidal TractsSignal TransductionSpinal CordcorticospinalDREADDlight-sheet microscopymotor controlretrograde gene therapysupraspinal centers

Identifiers

PMID30341180
PMCPMC6284107
OpenAlexW2802035465

What OpenQuestion holds

Textmetadata
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.