Evidence map›Paper›PMID 33259856›Full record

ArticleJournal of molecular and cellular cardiology2021

Protective role of ErbB3 signaling in myeloid cells during adaptation to cardiac pressure overload.

Haifeng Yin, Amanda J Favreau-Lessard, Joanne T deKay, Yodit R Herrmann, Michael P Robich, Robert A Koza, Igor Prudovsky, Douglas B Sawyer, Sergey Ryzhov

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

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  9. Mechanisms and strategies for a therapeutic cardiac immune response.Journal of molecular and cellular cardiology · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Haifeng YinMaine Medical Center Research Institute, Scarborough, ME, United States of America.
Amanda J Favreau-LessardMaine Medical Center Research Institute, Scarborough, ME, United States of America.
Joanne T deKayMaine Medical Center Research Institute, Scarborough, ME, United States of America.
Yodit R HerrmannMaine Medical Center Research Institute, Scarborough, ME, United States of America.
Michael P RobichMaine Medical Center Research Institute, Scarborough, ME, United States of America; Maine Medical Center, Cardiovascular Institute, Portland, ME, United States of America.
Robert A KozaMaine Medical Center Research Institute, Scarborough, ME, United States of America.
Igor PrudovskyMaine Medical Center Research Institute, Scarborough, ME, United States of America.
Douglas B SawyerMaine Medical Center Research Institute, Scarborough, ME, United States of America; Maine Medical Center, Cardiovascular Institute, Portland, ME, United States of America.
Sergey RyzhovMaine Medical Center Research Institute, Scarborough, ME, United States of America. Electronic address: sryzhov@mmc.org.
Maine Medical Center · USMaine Medical Center Research Institute · US

Funding

Understanding Factors Influencing COVID-19 Testing and Vaccination in Immigrant Low-income and Homeless Populations and Testing Targeted InterventionsU54GM115516 · NIGMS · MAINEHEALTH · PI Jan Kirk Carney · 2017 to 2026
$51.6M
Optimizing Cardiovascular Stem Cells for Cardiac Repair and RegenerationU01HL100398 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HATZOPOULOS, ANTONIS · 2009 to 2015
$8.0M
Progenitor Cell Analysis CoreP30GM106391 · NIGMS · MAINEHEALTH · PI FRIESEL, ROBERT E · 2013 to 2017
$5.7M
Neuregulin signaling in myeloid cellsR01HL136560 · NHLBI · MAINEHEALTH · PI Sergey Ryzhov · 2017 to 2026
$3.3M
Molecular determinants of the fate of human heart mesenchymal progenitor cellsR01HL139887 · NHLBI · MAINEHEALTH · PI SAWYER, DOUGLAS B, VARY, CALVIN PARDEE HULL · 2019 to 2022
$2.0M
NHLBI NIH HHS R01 HL136560NHLBI NIH HHS R01 HL139887NHLBI NIH HHS U01 HL100398NIGMS NIH HHS P30 GM106391NIGMS NIH HHS U54 GM115516
6 · The paper itself

Abstract

backgroundMyeloid cells play an important role in a wide variety of cardiovascular disorders, including both ischemic and non-ischemic cardiomyopathies. Neuregulin-1 (NRG-1)/ErbB signaling has recently emerged as an important factor contributing to the control of inflammatory activation of myeloid cells after an ischemic injury. However, the role of ErbB signaling in myeloid cells in non-ischemic cardiomyopathy is not fully understood. This study investigated the role of ErbB3 receptors in the regulation of early adaptive response using a mouse model of transverse aortic constriction (TAC) for non-ischemic cardiomyopathy. METHODS AND

resultsTAC surgery was performed in groups of age- and sex-matched myeloid cell-specific ErbB3-deficient mice (ErbB3

conclusionOur data demonstrate the crucial role of myeloid cell-specific ErbB3 signaling in the cardiac accumulation of myeloid cells, which contributes to the activation of cardiac endothelial cells and fibroblasts and development of an early adaptive response to cardiac pressure overload in male mice.

Indexed as

Adaptation, PhysiologicalDisease Models, AnimalAnimalsCardiomegalyFemaleHypertrophy, Left VentricularMaleMiceMice, KnockoutMyeloid CellsReceptor, ErbB-3ErbB3 protein, mouseReceptor, ErbB-3ErbB3Insulin growth factor-1Myeloid cellsNon-ischemic cardiomyopathyTransverse aortic constriction

Identifiers

PMID33259856
PMCPMC7981250
OpenAlexW3109302029

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.