Evidence map›Paper›PMID 36515985›Full record

ArticleeLife2022

The injured sciatic nerve atlas (iSNAT), insights into the cellular and molecular basis of neural tissue degeneration and regeneration.

Xiao-Feng Zhao, Lucas D Huffman, Hannah Hafner, Mitre Athaiya, Matthew C Finneran, Ashley L Kalinski, Rafi Kohen, Corey Flynn, Ryan Passino, Craig N Johnson and 7 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
7.8field-weighted citation impact, top 1% 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

47 citing papers in PubMed, 84 citations in OpenAlex.

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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

17 authors at 3 institutions in 1 country.

Xiao-Feng Zhao *Department of Cell and Developmental Biology, University of Michigan-Ann Arbor, Ann Arbor, United States.ORCID https://orcid.org/0000-0002-7574-7163
Lucas D Huffman *Department of Cell and Developmental Biology, University of Michigan-Ann Arbor, Ann Arbor, United States.ORCID https://orcid.org/0000-0002-7779-086X
Hannah Hafner *Department of Cell and Developmental Biology, University of Michigan-Ann Arbor, Ann Arbor, United States.
Mitre AthaiyaDepartment of Cell and Developmental Biology, University of Michigan-Ann Arbor, Ann Arbor, United States.
Matthew C FinneranDepartment of Cell and Developmental Biology, University of Michigan-Ann Arbor, Ann Arbor, United States.
Ashley L KalinskiDepartment of Cell and Developmental Biology, University of Michigan-Ann Arbor, Ann Arbor, United States.ORCID https://orcid.org/0000-0001-7611-0810
Rafi KohenDepartment of Cell and Developmental Biology, University of Michigan-Ann Arbor, Ann Arbor, United States.
Corey FlynnDepartment of Cell and Developmental Biology, University of Michigan-Ann Arbor, Ann Arbor, United States.ORCID https://orcid.org/0000-0001-5811-7269
Ryan PassinoDepartment of Cell and Developmental Biology, University of Michigan-Ann Arbor, Ann Arbor, United States.
Craig N JohnsonDepartment of Cell and Developmental Biology, University of Michigan-Ann Arbor, Ann Arbor, United States.ORCID https://orcid.org/0000-0003-3955-7394
David KohrmanKresge Hearing Institute, University of Michigan-Ann Arbor, Ann Arbor, United States.
Riki KawaguchiDepartments of Psychiatry and Neurology, University of California, Los Angeles, Los Angeles, United States.
Lynda J S YangDepartment of Neurosurgery, University of Michigan-Ann Arbor, Ann Arbor, United States.
Jeffery L TwissDepartment of Biological Sciences, University of South Carolina, Columbia, United States.ORCID https://orcid.org/0000-0001-7875-6682
Daniel H GeschwindDepartment of Neurology, Program in Neurogenetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, United States.ORCID https://orcid.org/0000-0003-2896-3450
Gabriel CorfasNeuroscience Graduate Program, University of Michigan-Ann Arbor, Ann Arbor, United States.ORCID https://orcid.org/0000-0001-5412-9473
Roman J GigerDepartment of Cell and Developmental Biology, University of Michigan-Ann Arbor, Ann Arbor, United States.ORCID https://orcid.org/0000-0002-2926-3336
University of Michigan · USUniversity of California, Los Angeles · USUniversity of South Carolina · US

Funding

TRAINING IN CLINICAL AND BASIC NEUROSCIENCET32NS007222 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Henry L Paulson · 1985 to 2026
$8.0M
The Roles of Neuronal Activity in Peripheral Nerve MyelinationR01DC018500 · NIDCD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CORFAS, GABRIEL · 2020 to 2024
$2.6M
Inhibitors of Synaptogenesis and Mental HealthR01MH119346 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GIGER, ROMAN JENO · 2019 to 2023
$2.6M
Training Program in Translational ResearchT32GM113900 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIEBERMAN, ANDREW P, NIKOLOVSKA-COLESKA, ZANETA · 2016 to 2020
$991k
(PQD4) Epigenetic loss of heterozygosity as a driver of the cancer field effectR21CA185000 · NCI · DANA-FARBER CANCER INST · PI GIMELBRANT, ALEXANDER, ZHAO, JEAN · 2014 to 2015
$406k
NCI NIH HHS R21 CA185000NIDCD NIH HHS R01 DC018500NIGMS NIH HHS T32 GM113900NIH HHS T32 GM113900NIMH NIH HHS R01 MH119346NINDS NIH HHS T32 NS007222
6 · The paper itself

Abstract

Upon trauma, the adult murine peripheral nervous system (PNS) displays a remarkable degree of spontaneous anatomical and functional regeneration. To explore extrinsic mechanisms of neural repair, we carried out single-cell analysis of naïve mouse sciatic nerve, peripheral blood mononuclear cells, and crushed sciatic nerves at 1 day, 3 days, and 7 days following injury. During the first week, monocytes and macrophages (Mo/Mac) rapidly accumulate in the injured nerve and undergo extensive metabolic reprogramming. Proinflammatory Mo/Mac with a high glycolytic flux dominate the early injury response and rapidly give way to inflammation resolving Mac, programmed toward oxidative phosphorylation. Nerve crush injury causes partial leakiness of the blood-nerve barrier, proliferation of endoneurial and perineurial stromal cells, and entry of opsonizing serum proteins. Micro-dissection of the nerve injury site and distal nerve, followed by single-cell RNA-sequencing, identified distinct immune compartments, triggered by mechanical nerve wounding and Wallerian degeneration, respectively. This finding was independently confirmed with

Indexed as

Peripheral Nerve InjuriesWallerian DegenerationAnimalsArmadillo Domain ProteinsCytoskeletal ProteinsLeukocytes, MononuclearMiceNerve CrushNerve DegenerationNerve RegenerationSciatic NerveArmadillo Domain ProteinsCytoskeletal ProteinsSARM1 protein, mouseimmunologyinflammationmouseneuroscienceparabiosisregenerationsciatic nervesingle-cell RNA seqWallerian degeneration

Identifiers

PMID36515985
PMCPMC9829412
OpenAlexW4311404511

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.