Evidence map›Paper›PMID 29677517›Full record

ArticleCell2018

GPR68 Senses Flow and Is Essential for Vascular Physiology.

Jie Xu, Jayanti Mathur, Emilie Vessières, Scott Hammack, Keiko Nonomura, Julie Favre, Linda Grimaud, Matt Petrus, Allain Francisco, Jingyuan Li and 15 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 174 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
174citing papers in PubMed, 1 pooled it
18.6field-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

174 citing papers in PubMed, 1 synthesis or guideline pooled it, 316 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  5. Article
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  7. Article
  8. Review
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  11. Article
  12. Article
  13. Mechanobiology of the Nucleolus.Biology of the cell · 2026
    Review
  14. Article
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  17. Article
  18. Article
  19. Article
  20. PIPProceedings of the National Academy of Sciences of the United States of America · 2025
    Article

114 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 7 institutions in 2 countries.

Jie XuGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
Jayanti MathurGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
Emilie VessièresMITOVASC Institute, CARFI Facility, CNRS UMR 6015, INSERM U1083, Angers University, Angers, France.
Scott HammackGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
Keiko NonomuraDoris Neuroscience Center, Howard Hughes Medical Institute, the Scripps Research Institute, La Jolla, CA 92037, USA.
Julie FavreMITOVASC Institute, CARFI Facility, CNRS UMR 6015, INSERM U1083, Angers University, Angers, France.
Linda GrimaudMITOVASC Institute, CARFI Facility, CNRS UMR 6015, INSERM U1083, Angers University, Angers, France.
Matt PetrusGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
Allain FranciscoDoris Neuroscience Center, Howard Hughes Medical Institute, the Scripps Research Institute, La Jolla, CA 92037, USA.
Jingyuan LiGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
Van LeeGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
Fu-Li XiangGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
James K MainquistGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
Stuart M CahalanDoris Neuroscience Center, Howard Hughes Medical Institute, the Scripps Research Institute, La Jolla, CA 92037, USA.
Anthony P OrthGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
John R WalkerGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
Shang MaDoris Neuroscience Center, Howard Hughes Medical Institute, the Scripps Research Institute, La Jolla, CA 92037, USA.
Viktor LukacsDoris Neuroscience Center, Howard Hughes Medical Institute, the Scripps Research Institute, La Jolla, CA 92037, USA.
Laura BordoneGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
Michael BandellGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
Bryan LaffitteGenomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
Yan XuDepartment of Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Shu ChienDepartments of Bioengineering and Medicine, and Institute of Engineering in Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Daniel HenrionMITOVASC Institute, CARFI Facility, CNRS UMR 6015, INSERM U1083, Angers University, Angers, France.
Ardem PatapoutianDoris Neuroscience Center, Howard Hughes Medical Institute, the Scripps Research Institute, La Jolla, CA 92037, USA. Electronic address: ardem@scripps.edu.
Genomics Institute of the Novartis Research Foundation · USHoward Hughes Medical Institute · USScripps Research Institute · USInserm · FRUniversité d'Angers · FRIndiana University School of MedicineUniversity of California, San Diego · US

Funding

Role of mechanically activated ion channels in somatosensationR01DE022358 · NIDCR · SCRIPPS RESEARCH INSTITUTE, THE · PI PATAPOUTIAN, ARDEM · 2012 to 2020
$5.3M
Howard Hughes Medical InstituteNIDCR NIH HHS R01 DE022358
6 · The paper itself

Abstract

Mechanotransduction plays a crucial role in vascular biology. One example of this is the local regulation of vascular resistance via flow-mediated dilation (FMD). Impairment of this process is a hallmark of endothelial dysfunction and a precursor to a wide array of vascular diseases, such as hypertension and atherosclerosis. Yet the molecules responsible for sensing flow (shear stress) within endothelial cells remain largely unknown. We designed a 384-well screening system that applies shear stress on cultured cells. We identified a mechanosensitive cell line that exhibits shear stress-activated calcium transients, screened a focused RNAi library, and identified GPR68 as necessary and sufficient for shear stress responses. GPR68 is expressed in endothelial cells of small-diameter (resistance) arteries. Importantly, Gpr68-deficient mice display markedly impaired acute FMD and chronic flow-mediated outward remodeling in mesenteric arterioles. Therefore, GPR68 is an essential flow sensor in arteriolar endothelium and is a critical signaling component in cardiovascular pathophysiology.

Indexed as

Mechanotransduction, CellularRNA InterferenceAnimalsBiocompatible MaterialsCalciumCell Line, TumorEndothelial CellsEndothelium, VascularHEK293 CellsHumansHuman Umbilical Vein Endothelial CellsHydrogen-Ion ConcentrationMesenteric ArteriesMiceMice, Inbred C57BLMice, KnockoutBiocompatible MaterialsCalciumGPR68 protein, humanGPR68 protein, mouseNitric OxideReceptors, G-Protein-CoupledRNA, Small Interferingblood flowGPCRmechanosensationmechanotransductionoutward remodelingshear stressvascular biologyvasodilation

Identifiers

PMID29677517
PMCPMC5951615
OpenAlexW2799943205

What OpenQuestion 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 OpenQuestion graph.