Evidence map›Paper›PMID 26351678›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Piezo1 regulates mechanotransductive release of ATP from human RBCs.

Eyup Cinar, Sitong Zhou, James DeCourcey, Yixuan Wang, Richard E Waugh, Jiandi Wan

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 124 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
124citing papers in PubMed, 1 pooled it
8.9field-weighted citation impact, top 2% 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

124 citing papers in PubMed, 1 synthesis or guideline pooled it, 193 citations in OpenAlex.

  1. Pooled it
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  13. Mechanosensitive ion channels and inflammation: key links in cellular signal transduction.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
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  18. Cellular mechanisms of traumatic brain injury.npj biological physics and mechanics · 2025
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64 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

6 authors at 2 institutions in 2 countries.

Eyup CinarMicrosystems Engineering, Rochester Institute of Technology, Rochester, NY 14623;
Sitong ZhouMicrosystems Engineering, Rochester Institute of Technology, Rochester, NY 14623;
James DeCourceyDepartment of Biology, Rochester Institute of Technology, Rochester, NY 14623;
Yixuan WangMicrosystems Engineering, Rochester Institute of Technology, Rochester, NY 14623; School of Mechanical Engineering, University of Science and Technology, Beijing 100083, China;
Richard E WaughDepartment of Biomedical Engineering, University of Rochester, Rochester, NY 14627.
Jiandi WanMicrosystems Engineering, Rochester Institute of Technology, Rochester, NY 14623; jdween@rit.edu.
Rochester Institute of Technology · USUniversity of Rochester · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Piezo proteins (Piezo1 and Piezo2) are recently identified mechanically activated cation channels in eukaryotic cells and associated with physiological responses to touch, pressure, and stretch. In particular, human RBCs express Piezo1 on their membranes, and mutations of Piezo1 have been linked to hereditary xerocytosis. To date, however, physiological functions of Piezo1 on normal RBCs remain poorly understood. Here, we show that Piezo1 regulates mechanotransductive release of ATP from human RBCs by controlling the shear-induced calcium (Ca(2+)) influx. We find that, in human RBCs treated with Piezo1 inhibitors or having mutant Piezo1 channels, the amounts of shear-induced ATP release and Ca(2+) influx decrease significantly. Remarkably, a critical extracellular Ca(2+) concentration is required to trigger significant ATP release, but membrane-associated ATP pools in RBCs also contribute to the release of ATP. Our results show how Piezo1 channels are likely to function in normal RBCs and suggest a previously unidentified mechanotransductive pathway in ATP release. Thus, we anticipate that the study will impact broadly on the research of red cells, cellular mechanosensing, and clinical studies related to red cell disorders and vascular disease.

Indexed as

Mechanotransduction, CellularAdenosine TriphosphateCalciumCalibrationErythrocyte MembraneErythrocytesExtracellular SpaceHumansIon ChannelsMicrofluidicsModels, BiologicalShear StrengthAdenosine TriphosphateCalciumIon ChannelsPIEZO1 protein, humanATP releasecalcium fluxmechanosensingPizeo1RBCs

Identifiers

PMID26351678
PMCPMC4586865
OpenAlexW1684606992

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.