Evidence map›Paper›PMID 35903933›Full record

ArticleGlia2022

Piezo channels contribute to the regulation of myelination in Schwann cells.

Jenica Acheta, Urja Bhatia, Jeanette Haley, Jiayue Hong, Kyle Rich, Rachel Close, Marie E Bechler, Sophie Belin, Yannick Poitelon

Open access · greenAbstract read
In one paragraph

Article in Glia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
8.7field-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

50 citing papers in PubMed, 80 citations in OpenAlex.

  1. Review
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  3. Article
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  6. Review
  7. Review
  8. Article
  9. Article
  10. PIEZO1 enhances pancreatic cancer neurotropism.Cancer cell international · 2026
    Article
  11. Article
  12. Review
  13. Article
  14. Mechanobiology of Myelin Generation/Regeneration in Health and Disease.Results and problems in cell differentiation · 2026
    Review
  15. Review
  16. Review
  17. Article
  18. Review
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  20. 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

9 authors at 2 institutions in 1 country.

Jenica AchetaDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, New York, USA.
Urja BhatiaDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, New York, USA.
Jeanette HaleyDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, New York, USA.
Jiayue HongDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, New York, USA.
Kyle RichDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, New York, USA.
Rachel CloseDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, New York, USA.
Marie E BechlerDepartment of Cell and Developmental Biology, State University of New York Upstate Medical University, Syracuse, New York, USA.ORCID 0000-0002-2443-1353
Sophie BelinDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, New York, USA.ORCID 0000-0003-2686-7318
Yannick PoitelonDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, New York, USA.ORCID 0000-0001-9868-1569
Albany Medical Center Hospital · USSUNY Upstate Medical University · US

Funding

Transduction of Mechanical Stimuli in Myelination and Peripheral Nerve RepairR01NS110627 · NINDS · ALBANY MEDICAL COLLEGE · PI POITELON, YANNICK · 2020 to 2024
$2.1M
NINDS NIH HHS R01 NS110627
6 · The paper itself

Abstract

Peripheral nerves and Schwann cells have to sustain constant mechanical constraints, caused by developmental growth as well as stretches associated with movements of the limbs and mechanical compressions from daily activities. In Schwann cells, signaling molecules sensitive to stiffness or stretch of the extracellular matrix, such as YAP/TAZ, have been shown to be critical for Schwann cell development and peripheral nerve regeneration. YAP/TAZ have also been suggested to contribute to tumorigenesis, neuropathic pain, and inherited disorders. Yet, the role of mechanosensitive ion channels in myelinating Schwann cells is vastly unexplored. Here we comprehensively assessed the expression of mechanosensitive ion channels in Schwann cells and identified that PIEZO1 and PIEZO2 are among the most abundant mechanosensitive ion channels expressed by Schwann cells. Using classic genetic ablation studies, we show that PIEZO1 is a transient inhibitor of radial and longitudinal myelination in Schwann cells. Contrastingly, we show that PIEZO2 may be required for myelin formation, as the absence of PIEZO2 in Schwann cells delays myelin formation. We found an epistatic relationship between PIEZO1 and PIEZO2, at both the morphological and molecular levels. Finally, we show that PIEZO1 channels affect the regulation of YAP/TAZ activation in Schwann cells. Overall, we present here the first demonstration that PIEZO1 and PIEZO2 contribute to mechanosensation in Schwann cells as well myelin development in the peripheral nervous system.

Indexed as

Ion ChannelsSchwann CellsMyelin SheathNeurogenesisIon ChannelsFam38aFam38bmyelinPIEZO1PIEZO2Schwann cell

Identifiers

PMID35903933
PMCPMC10638658
OpenAlexW4288714732

What Socratic holds

Textmetadata
LicenceTDM
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.