Evidence map›Paper›PMID 26071893›Full record

ArticleJournal of molecular and cellular cardiology2015

Inhibition of Wnt6 by Sfrp2 regulates adult cardiac progenitor cell differentiation by differential modulation of Wnt pathways.

Jeffrey Schmeckpeper, Amanda Verma, Lucy Yin, Farideh Beigi, Lunan Zhang, Alan Payne, Zhiping Zhang, Richard E Pratt, Victor J Dzau, Maria Mirotsou

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 41 citations in OpenAlex.

  1. Reversal of injury-induced fibrosis and anal sphincter muscle dysfunction by sFRP2 in rabbits.American journal of physiology. Gastrointestinal and liver physiology · 2026
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  10. A role for Sfrp2 in cardiomyogenesis in vivo.Proceedings of the National Academy of Sciences of the United States of America · 2021
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  15. Article
  16. Multiple Roles of sFRP2 in Cardiac Development and Cardiovascular Disease.International journal of biological sciences · 2020
    Review
  17. Role of Sfrps in cardiovascular disease.Therapeutic advances in chronic disease · 2020
    Review
  18. Expression and Function of WNT6: From Development to Disease.Frontiers in cell and developmental biology · 2020
    Review
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  20. Article
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

10 authors at 1 institution in 1 country.

Jeffrey SchmeckpeperDivision of Cardiology, Department of Medicine, Duke University Medical Center & Duke Cardiovascular Research Center, Durham, NC 27710, USA.
Amanda VermaDivision of Cardiology, Department of Medicine, Duke University Medical Center & Duke Cardiovascular Research Center, Durham, NC 27710, USA.
Lucy YinDivision of Cardiology, Department of Medicine, Duke University Medical Center & Duke Cardiovascular Research Center, Durham, NC 27710, USA.
Farideh BeigiDivision of Cardiology, Department of Medicine, Duke University Medical Center & Duke Cardiovascular Research Center, Durham, NC 27710, USA.
Lunan ZhangDivision of Cardiology, Department of Medicine, Duke University Medical Center & Duke Cardiovascular Research Center, Durham, NC 27710, USA.
Alan PayneDivision of Cardiology, Department of Medicine, Duke University Medical Center & Duke Cardiovascular Research Center, Durham, NC 27710, USA.
Zhiping ZhangDivision of Cardiology, Department of Medicine, Duke University Medical Center & Duke Cardiovascular Research Center, Durham, NC 27710, USA.
Richard E PrattDivision of Cardiology, Department of Medicine, Duke University Medical Center & Duke Cardiovascular Research Center, Durham, NC 27710, USA; Duke Cardiovascular Research Center, Durham, NC 27710, USA.
Victor J DzauDivision of Cardiology, Department of Medicine, Duke University Medical Center & Duke Cardiovascular Research Center, Durham, NC 27710, USA; Duke Cardiovascular Research Center, Durham, NC 27710, USA. Electronic address: victor.dzau@duke.edu.
Maria MirotsouDivision of Cardiology, Department of Medicine, Duke University Medical Center & Duke Cardiovascular Research Center, Durham, NC 27710, USA; Duke Cardiovascular Research Center, Durham, NC 27710, USA.
Duke Medical Center · US

Funding

X-RAY RESEARCH AND DEVELOPMENT WITH/WITHOUT LIVE ANIMALSP41RR005959 · NCRR · DUKE UNIVERSITY · PI DZAU, VICTOR J · 1990 to 2011
$16.0M
GENE THERAPY FOR LONG-TERM MYOCARDIAL PROTECTIONR01HL072010 · NHLBI · DUKE UNIVERSITY · PI DZAU, VICTOR J · 2003 to 2013
$4.5M
Sfrp2 as a Stem Cell Derived Paracrine Factor for CardioprotectionR01HL081744 · NHLBI · DUKE UNIVERSITY · PI DZAU, VICTOR J · 2006 to 2015
$3.8M
RENIN GENE EXPRESSION IN HYPERTENSIONR01HL035610 · NHLBI · STANFORD UNIVERSITY · PI DZAU, VICTOR J · 1985 to 2011
$3.6M
Homing and Genetic Modification of Mesenchymal Stem CellR01HL073219 · NHLBI · DUKE UNIVERSITY · PI DZAU, VICTOR J · 2003 to 2012
$3.5M
NCRR NIH HHS P41 RR005959NHLBI NIH HHS HL72010NHLBI NIH HHS HL73219NHLBI NIH HHS HL81744NHLBI NIH HHS R01 HL035610NHLBI NIH HHS R01 HL072010NHLBI NIH HHS R01 HL073219NHLBI NIH HHS R01 HL081744NHLBI NIH HHS R01 HL35610
6 · The paper itself

Abstract

Wnt signaling has recently emerged as an important regulator of cardiac progenitor cell proliferation and differentiation, but the exact mechanisms by which Wnt signaling modulates these effects are not known. Understanding these mechanisms is essential for advancing our knowledge of cardiac progenitor cell biology and applying this knowledge to enhance cardiac therapy. Here, we explored the effects of Sfrp2, a canonical Wnt inhibitor, in adult cardiac progenitor cell (CPC) differentiation and investigated the molecular mechanisms involved. Our data show that Sfrp2 treatment can promote differentiation of CPCs after ischemia-reperfusion injury. Treatment of CPCs with Sfrp2 inhibited CPC proliferation and primed them for cardiac differentiation. Sfrp2 binding to Wnt6 and inhibition of Wnt6 canonical pathway was essential for the inhibition of CPC proliferation. This inhibition of Wnt6 canonical signaling by Sfrp2 was important for activation of the non-canonical Wnt/Planar Cell Polarity (PCP) pathway through JNK, which in turn induced expression of cardiac transcription factors and CPC differentiation. Taken together, these results demonstrate a novel role of Sfrp2 and Wnt6 in regulating the dynamic process of CPC proliferation and differentiation, as well as providing new insights into the mechanisms of Wnt signaling in cardiac differentiation.

Indexed as

Cell DifferentiationAnimalsCell ProliferationCells, CulturedGene ExpressionMembrane ProteinsMiceMyocytes, CardiacProto-Oncogene ProteinsSecreted Frizzled-Related ProteinsStem CellsTranscriptional ActivationTranscription FactorsUp-RegulationWnt ProteinsWnt Signaling PathwayMembrane ProteinsProto-Oncogene ProteinsSecreted Frizzled-Related ProteinsSfrp2 protein, mouseTranscription FactorsWnt6 protein, mouseWnt ProteinsCardiac injuryCardiac progenitor cellsDifferentiationSfrp2Wnt signaling

Identifiers

PMID26071893
PMCPMC4838816
OpenAlexW1959889113

What OpenQuestion holds

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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.