Evidence map›Paper›PMID 39091840›Full record

ArticlebioRxiv : the preprint server for biology2024

Endothelial TRPV4/Cx43 Signaling Complex Regulates Vasomotor Tone in Resistance Arteries.

Pía C Burboa, Pablo S Gaete, Ping Shu, Priscila A Araujo, Annie V Beuve, Walter N Durán, Jorge E Contreras, Mauricio A Lillo

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Pía C BurboaDepartment of Pharmacology, Physiology and Neuroscience, Rutgers-New Jersey Medical School, Newark, NJ 07103, U.S.A.
Pablo S GaeteDepartment of Physiology and Membrane Biology, School of Medicine, University of California Davis, Davis, CA, U.S.A.
Ping ShuDepartment of Pharmacology, Physiology and Neuroscience, Rutgers-New Jersey Medical School, Newark, NJ 07103, U.S.A.
Priscila A AraujoDepartment of Physiology and Membrane Biology, School of Medicine, University of California Davis, Davis, CA, U.S.A.
Annie V BeuveDepartment of Pharmacology, Physiology and Neuroscience, Rutgers-New Jersey Medical School, Newark, NJ 07103, U.S.A.
Walter N DuránDepartment of Pharmacology, Physiology and Neuroscience, Rutgers-New Jersey Medical School, Newark, NJ 07103, U.S.A.
Jorge E ContrerasDepartment of Physiology and Membrane Biology, School of Medicine, University of California Davis, Davis, CA, U.S.A.
Mauricio A LilloDepartment of Pharmacology, Physiology and Neuroscience, Rutgers-New Jersey Medical School, Newark, NJ 07103, U.S.A.ORCID 0000-0002-2823-6619

Funding

Regulation of Soluble Guanylyl Cyclase, the NO-ReceptorR01GM067640 · NIGMS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI BEUVE, ANNIE V · 2003 to 2021
$5.8M
Gating and Regulation of Connexin HemichannelsR01GM099490 · NIGMS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI CONTRERAS, JORGE ENRIQUE · 2011 to 2025
$4.9M
NO signaling by a Soluble Guanylyl Cyclase-Thioredoxin transnitrosation complexR01GM112415 · NIGMS · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI BEUVE, ANNIE V · 2015 to 2023
$3.5M
Inactivation Mechanisms of Microvascular HyperpermeabilityR01HL146539 · NHLBI · RBHS-NEW JERSEY MEDICAL SCHOOL · PI DURAN, WALTER N. · 2020 to 2022
$1.9M
Connexin 43: a new player in Duchenne muscular dystrophy associated cardiomyopathyR01HL141170 · NHLBI · RBHS-NEW JERSEY MEDICAL SCHOOL · PI CONTRERAS, JORGE ENRIQUE, FRAIDENRAICH, DIEGO · 2018 to 2021
$1.6M
Role of S-nitrosylated Cx43 in normal cardiac contractilityR21HL163930 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CONTRERAS, JORGE ENRIQUE · 2022 to 2023
$451k
NHLBI NIH HHS R01 HL141170NHLBI NIH HHS R01 HL146539NHLBI NIH HHS R21 HL163930NIGMS NIH HHS R01 GM067640NIGMS NIH HHS R01 GM099490NIGMS NIH HHS R01 GM112415
6 · The paper itself

Abstract

S-nitrosylation of Cx43 gap junction channels critically regulates communication between smooth muscle cells and endothelial cells. This posttranslational modification also induces the opening of undocked Cx43 hemichannels. However, its specific impact on vasomotor regulation remains unclear. Considering the role of endothelial TRPV4 channel activation in promoting vasodilation through nitric oxide (NO) production, we investigated the direct modulation of endothelial Cx43 hemichannels by TRPV4 channel activation. Using the proximity ligation assay, we identify that Cx43 and TRPV4 are found in close proximity in the endothelium of resistance arteries. In primary endothelial cell cultures from resistance arteries (ECs), GSK-induced TRPV4 activation enhances eNOS activity, increases NO production, and opens Cx43 hemichannels via direct S-nitrosylation. Notably, the elevated intracellular Ca

Indexed as

CaveolaeECshyperpolarizationresting membrane potential

Identifiers

PMID39091840
PMCPMC11291137

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.