Evidence map›Paper›PMID 35858549›Full record

ArticleCell reports2022

Sensory neurons display cell-type-specific vulnerability to loss of neuron-glia interactions.

Benayahu Elbaz, Lite Yang, Maia Vardy, Sara Isaac, Braesen L Rader, Riki Kawaguchi, Maria Traka, Clifford J Woolf, William Renthal, Brian Popko

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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  13. Transcriptional profiles of non-neuronal and immune cells in mouse trigeminal ganglia.Frontiers in pain research (Lausanne, Switzerland) · 2023
    Article
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

10 authors at 4 institutions in 2 countries.

Benayahu ElbazDepartment of Neurology, Northwestern Feinberg School of Medicine, Chicago, IL, USA. Electronic address: benayahu.elbaz-eilon@northwestern.edu.
Lite YangDepartment of Neurology, Brigham and Women's Hospital and Harvard Medical School, 60 Fenwood Road, Boston, MA 02115, USA.
Maia VardyDepartment of Neurology, Northwestern Feinberg School of Medicine, Chicago, IL, USA.
Sara IsaacDepartment of Cell and Developmental Biology, The Alexander Silberman Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem, Israel.
Braesen L RaderDepartment of Neurology, Northwestern Feinberg School of Medicine, Chicago, IL, USA.
Riki KawaguchiProgram in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Maria TrakaDepartment of Anatomy, College of Graduate Studies, Midwestern University, Downers Grove, IL, USA.
Clifford J WoolfDepartment of Neurobiology, Harvard Medical School, 220 Longwood Avenue, Boston, MA 02115, USA; F.M. Kirby Neurobiology Center, Boston Children's Hospital, 3 Blackfan Circle, Boston, MA 02115, USA.
William RenthalDepartment of Neurology, Brigham and Women's Hospital and Harvard Medical School, 60 Fenwood Road, Boston, MA 02115, USA.
Brian PopkoDepartment of Neurology, Northwestern Feinberg School of Medicine, Chicago, IL, USA. Electronic address: brian.popko@northwestern.edu.
Northwestern University · USHebrew University of Jerusalem · ILMidwestern University · USUniversity of California, Los Angeles · US

Funding

Unravelling Mechanisms and Novel Therapeutic Targets for Peripheral Neuropathy and Neuropathic Pain (Diversity Supplement)R35NS105076 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI WOOLF, CLIFFORD J · 2018 to 2025
$9.5M
Genetic Analysis and Manipulation Core (GAEC)P50HD105351 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Hisashi Umemori · 2021 to 2026
$9.4M
Targeting the integrated stress response to protect oligodendrocyte lineage cells - Resubmission 01R01NS034939 · NINDS · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI POPKO, BRIAN J · 1997 to 2024
$7.5M
Next Generation Gene Therapy for Refractory PainR01NS119476 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI William Russell Renthal · 2022 to 2026
$3.4M
ZFP24 Control of the myelination program of oligodendrocytesR01NS067550 · NINDS · UNIVERSITY OF CHICAGO · PI ELBAZ-EILON, BENAYAHU · 2009 to 2024
$3.4M
Epigenomic labeling of cells that drive drug abuse behaviorDP1DA054343 · NIDA · BRIGHAM AND WOMEN'S HOSPITAL · PI RENTHAL, WILLIAM RUSSELL · 2021 to 2025
$2.7M
Exploring the origins of myelin abnormalities in normal ageing and in vascular dementiaRF1AG072080 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI FLANAGAN, MARGARET E, POPKO, BRIAN J · 2021 to 2021
$2.2M
Regulation of CD4+ T cell-mediated Demyelination Following Oligo AblationR01NS099334 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MILLER, STEPHEN D, POPKO, BRIAN J · 2017 to 2021
$2.1M
Reversible mRNA methylation in oligodendrocyte development and CNS myelinationR01NS109372 · NINDS · UNIVERSITY OF CHICAGO · PI POPKO, BRIAN J · 2018 to 2022
$1.7M
Exploring the origins of myelin abnormalities in normal ageing and in vascular dementiaR01AG072080 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI FLANAGAN, MARGARET E, POPKO, BRIAN J · 2024 to 2025
$1.4M
CONTROL OF LONG GENE EXPRESSION AS A NOVEL THERAPEUTIC APPROACH FOR RETT SYNDROMEK08NS101064 · NINDS · HARVARD MEDICAL SCHOOL · PI RENTHAL, WILLIAM RUSSELL · 2017 to 2021
$940k
nvestigating the role of neuroinflammation in Limbic-predominant age related TDP43 encephalopathyK08AG065463 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI FLANAGAN, MARGARET E · 2020 to 2024
$816k
NIA NIH HHS K08 AG065463NIA NIH HHS R01 AG072080NIA NIH HHS RF1 AG072080NICHD NIH HHS P50 HD105351NIDA NIH HHS DP1 DA054343NINDS NIH HHS K08 NS101064NINDS NIH HHS R01 NS034939NINDS NIH HHS R01 NS067550NINDS NIH HHS R01 NS099334NINDS NIH HHS R01 NS109372NINDS NIH HHS R01 NS119476NINDS NIH HHS R35 NS105076
6 · The paper itself

Abstract

Peripheral nervous system (PNS) injuries initiate transcriptional changes in glial cells and sensory neurons that promote axonal regeneration. While the factors that initiate the transcriptional changes in glial cells are well characterized, the full range of stimuli that initiate the response of sensory neurons remain elusive. Here, using a genetic model of glial cell ablation, we find that glial cell loss results in transient PNS demyelination without overt axonal loss. By profiling sensory ganglia at single-cell resolution, we show that glial cell loss induces a transcriptional injury response preferentially in proprioceptive and Aβ RA-LTMR neurons. The transcriptional response of sensory neurons to mechanical injury has been assumed to be a cell-autonomous response. By identifying a similar response in non-injured, demyelinated neurons, our study suggests that this represents a non-cell-autonomous transcriptional response of sensory neurons to glial cell loss and demyelination.

Indexed as

Demyelinating DiseasesNeurogliaHumansPeripheral Nervous SystemSensory Receptor CellsCP: Neuroscience

Identifiers

PMID35858549
PMCPMC9354470
OpenAlexW4286249805

What Socratic 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 Socratic graph.