Evidence map›Paper›PMID 38646936›Full record

ArticleJCI insight2024

Fabry disease Schwann cells release p11 to induce sensory neuron hyperactivity.

Tyler B Waltz, Dongman Chao, Eve K Prodoehl, Jonathan D Enders, Vanessa L Ehlers, Bhavya S Dharanikota, Nancy M Dahms, Elena Isaeva, Quinn H Hogan, Bin Pan and 1 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Pathogenic mechanisms in Fabry disease.Frontiers in medicine · 2026
    Review
  7. Not Just Neurons: Pain Is Orchestrated in Partnership with Many Non-neuronal Cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Review
  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 2 countries.

Tyler B WaltzDepartment of Cell Biology, Neurobiology & Anatomy.
Dongman ChaoDepartment of Anesthesiology; and.
Eve K ProdoehlDepartment of Cell Biology, Neurobiology & Anatomy.
Jonathan D EndersDepartment of Cell Biology, Neurobiology & Anatomy.
Vanessa L EhlersDepartment of Cell Biology, Neurobiology & Anatomy.
Bhavya S DharanikotaDepartment of Cell Biology, Neurobiology & Anatomy.
Nancy M DahmsDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Elena IsaevaDepartment of Cell Biology, Neurobiology & Anatomy.
Quinn H HoganDepartment of Anesthesiology; and.
Bin PanDepartment of Anesthesiology; and.
Cheryl L StuckyDepartment of Cell Biology, Neurobiology & Anatomy.
Institute of Cell Biology and Neurobiology · ITMedical College of Wisconsin · US

Funding

Gene targeted rat resource for the study of complex diseaseR24HL114474 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI DWINELL, MELINDA R · 2013 to 2017
$8.7M
Medical Scientist Training ProgramT32GM080202 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI BARBIERI, JOSEPH T, SALZMAN, NITA H · 2010 to 2024
$5.7M
Pain Mechanisms in Fabry DiseaseR37NS108278 · NINDS · MEDICAL COLLEGE OF WISCONSIN · PI STUCKY, CHERYL LOUISE · 2019 to 2025
$5.6M
Fabry Disease in the Gla Knockout Rat: Development of Novel Protein TherapeuticsR21NS095627 · NINDS · MEDICAL COLLEGE OF WISCONSIN · PI DAHMS, NANCY M. · 2015 to 2016
$369k
Peripheral Neuronal and Non-neuronal Mechanisms of Fabry Disease PainF31NS122380 · NINDS · MEDICAL COLLEGE OF WISCONSIN · PI WALTZ, TYLER B. · 2022 to 2023
$81k
NHLBI NIH HHS R24 HL114474NIGMS NIH HHS T32 GM080202NINDS NIH HHS F31 NS122380NINDS NIH HHS R21 NS095627NINDS NIH HHS R37 NS108278
6 · The paper itself

Abstract

Patients with Fabry disease suffer from chronic debilitating pain and peripheral sensory neuropathy with minimal treatment options, but the cellular drivers of this pain are unknown. Here, we propose a mechanism we believe to be novel in which altered signaling between Schwann cells and sensory neurons underlies the peripheral sensory nerve dysfunction we observed in a genetic rat model of Fabry disease. Using in vivo and in vitro electrophysiological recordings, we demonstrated that Fabry rat sensory neurons exhibited pronounced hyperexcitability. Schwann cells probably contributed to this finding because application of mediators released from cultured Fabry Schwann cells induced spontaneous activity and hyperexcitability in naive sensory neurons. We examined putative algogenic mediators using proteomic analysis and found that Fabry Schwann cells released elevated levels of the protein p11 (S100A10), which induced sensory neuron hyperexcitability. Removal of p11 from Fabry Schwann cell media caused hyperpolarization of neuronal resting membrane potentials, indicating that p11 may contribute to the excessive neuronal excitability caused by Fabry Schwann cells. These findings demonstrate that sensory neurons from rats with Fabry disease exhibit hyperactivity caused in part by Schwann cell release of the protein p11.

Indexed as

Disease Models, AnimalFabry DiseaseSchwann CellsSensory Receptor CellsAnimalsCells, CulturedFemaleMaleProteomicsRatsRats, Sprague-DawleyS100 Calcium Binding Protein A10S100 Calcium Binding Protein A10Ion channelsNeurological disordersNeurosciencePain

Identifiers

PMID38646936
PMCPMC11141882
OpenAlexW4395054601

What OpenQuestion holds

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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.