Evidence map›Paper›PMID 31390561›Full record

ArticleCell reports2019

Select Septate Junction Proteins Direct ROS-Mediated Paracrine Regulation of Drosophila Cardiac Function.

Hui-Ying Lim, Hong Bao, Ying Liu, Weidong Wang

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Analysis of the Ubiquitylomic Responses toJournal of inflammation research · 2022
    Article
  5. Article
  6. Review
  7. Review
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

4 authors at 1 institution in 1 country.

Hui-Ying LimDepartment of Physiology, University of Oklahoma Health Science Center, Oklahoma City, OK, USA. Electronic address: hlim@ouhsc.edu.
Hong BaoDepartment of Physiology, University of Oklahoma Health Science Center, Oklahoma City, OK, USA.
Ying LiuDepartment of Physiology, University of Oklahoma Health Science Center, Oklahoma City, OK, USA.
Weidong WangDepartment of Medicine, Section of Endocrinology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
University of Oklahoma Health Sciences Center · US

Funding

Understanding connective tissue development and disease with PDGFR-driven..... P20GM103636 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI THOMPSON, LINDA F · 2013 to 2023
$26.9M
ROS signaling, intercellular communication and heart development and functionR01HL128455 · NHLBI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI LIM, HUI-YING · 2015 to 2019
$2.0M
Cytoprotection and the mechanism of action of a natural product Khellin against ER stressR01DK116017 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI WANG, WEIDONG · 2018 to 2021
$1.6M
NHLBI NIH HHS R01 HL128455NIDDK NIH HHS R01 DK116017NIGMS NIH HHS P20 GM103636
6 · The paper itself

Abstract

Septate junction (SJ) complex proteins act in unison to provide a paracellular barrier and maintain structural integrity. Here, we identify a non-barrier role of two individual SJ proteins, Coracle (Cora) and Kune-kune (Kune). Reactive oxygen species (ROS)-p38 MAPK signaling in non-myocytic pericardial cells (PCs) is important for maintaining normal cardiac physiology in Drosophila. However, the underlying mechanisms remain unknown. We find that in PCs, Cora and Kune are altered in abundance in response to manipulations of ROS-p38 signaling. Genetic analyses establish Cora and Kune as key effectors of ROS-p38 signaling in PCs on proper heart function. We further determine that Cora regulates normal Kune levels in PCs, which in turn modulates normal Kune levels in the cardiomyocytes essential for proper heart function. Our results thereby reveal select SJ proteins Cora and Kune as signaling mediators of the PC-derived ROS regulation of cardiac physiology.

Indexed as

Paracrine CommunicationAnimalsClaudinsDrosophilaDrosophila ProteinsFemaleMaleMAP Kinase Signaling SystemMembrane ProteinsMyocytes, CardiacPericardiumReactive Oxygen SpeciesSignal TransductionTight JunctionsClaudinscora protein, DrosophilaDrosophila Proteinskune protein, DrosophilaMembrane ProteinsReactive Oxygen SpeciescardiomyocyteCoracleDrosophilaheart functionmitogen activated kinasep38pericardial nephrocytereactive oxygen speciesseptate junctionsignaling pathway

Identifiers

PMID31390561
PMCPMC6703176
OpenAlexW2965428656

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.