Evidence map›Paper›PMID 26564600›Full record

ArticleJournal of the American College of Cardiology2015

Enhanced Cardiac Regenerative Ability of Stem Cells After Ischemia-Reperfusion Injury: Role of Human CD34+ Cells Deficient in MicroRNA-377.

Darukeshwara Joladarashi, Venkata Naga Srikanth Garikipati, Rajarajan A Thandavarayan, Suresh K Verma, Alexander R Mackie, Mohsin Khan, Anna M Gumpert, Arvind Bhimaraj, Keith A Youker, Cesar Uribe and 4 more

Abstract read
In one paragraph

Article in Journal of the American College of Cardiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

46 citing papers in PubMed, 68 citations in OpenAlex.

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  9. The interplay of inflammation, exosomes and CaCardiovascular diabetology · 2023
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  13. MicroRNA-181c-5p modulates phagocytosis efficiency in bone marrow-derived macrophages.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Article
  14. Article
  15. Article
  16. Non-coding RNAs: Important participants in cardiac fibrosis.Frontiers in cardiovascular medicine · 2022
    Review
  17. miR-451-3p alleviates myocardial ischemia/reperfusion injury by inhibiting MAP1LC3B-mediated autophagy.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
    Article
  18. Article
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  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 1 country.

Darukeshwara JoladarashiDepartment of Cardiovascular Sciences, Center for Cardiovascular Regeneration, Houston Methodist Research Institute, Houston, Texas.
Venkata Naga Srikanth GarikipatiCenter for Translational Medicine, Temple University School of Medicine, Philadelphia, Pennsylvania.
Rajarajan A ThandavarayanDepartment of Cardiovascular Sciences, Center for Cardiovascular Regeneration, Houston Methodist Research Institute, Houston, Texas.
Suresh K VermaCenter for Translational Medicine, Temple University School of Medicine, Philadelphia, Pennsylvania.
Alexander R MackieFeinberg Cardiovascular Research Institute, Northwestern University, Chicago, Illinois.
Mohsin KhanCenter for Translational Medicine, Temple University School of Medicine, Philadelphia, Pennsylvania.
Anna M GumpertCenter for Translational Medicine, Temple University School of Medicine, Philadelphia, Pennsylvania.
Arvind BhimarajHouston Methodist DeBakey Heart & Vascular Center, Houston Methodist Hospital, Houston, Texas.
Keith A YoukerHouston Methodist DeBakey Heart & Vascular Center, Houston Methodist Hospital, Houston, Texas.
Cesar UribeHouston Methodist DeBakey Heart & Vascular Center, Houston Methodist Hospital, Houston, Texas.
Sahana Suresh BabuDepartment of Cardiovascular Sciences, Center for Cardiovascular Regeneration, Houston Methodist Research Institute, Houston, Texas.
Prince JeyabalDepartment of Cardiovascular Sciences, Center for Cardiovascular Regeneration, Houston Methodist Research Institute, Houston, Texas.
Raj KishoreCenter for Translational Medicine, Temple University School of Medicine, Philadelphia, Pennsylvania.
Prasanna KrishnamurthyDepartment of Cardiovascular Sciences, Center for Cardiovascular Regeneration, Houston Methodist Research Institute, Houston, Texas; Department of Cell and Developmental Biology, Department of Cardiothoracic Surgery, Weill Cornell Medical College, New York, New York. Electronic address: pkrishnamurthy@houstonmethodist.org.
Houston Methodist · USTemple University · USNorthwestern University · US

Funding

PKC alpha as a translational target in Heart FailureP01HL108806 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI RABINOWITZ, JOSEPH E · 2012 to 2016
$11.3M
Small Animal Surgery and HistologyP01HL108795 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOSORDO, DOUGLAS W · 2011 to 2015
$10.7M
TNF mRNA stability and restenosisR01HL091983 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KISHORE, RAJ · 2009 to 2022
$5.3M
Therapeutic Angiogenesis in Vascular Medicine IVR01HL053354 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KISHORE, RAJ · 1995 to 2015
$4.2M
microRNA mediation of Endothelial Progenitor Cell function in Myocardial IchemiaR01HL116729 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KRISHNAMURTHY, PRASANNA · 2013 to 2017
$1.9M
Pluripotent cell-derived exosomes as mediators of myocardial regenerationR01HL126186 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KISHORE, RAJ · 2015 to 2018
$1.6M
Novel approaches to ischemic tissue repairR01HL095874 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI KISHORE, RAJ · 2009 to 2012
$1.5M
Effect of chronic alcohol on ischemic injury and endothelial cellsR01HL105597 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KISHORE, RAJ · 2011 to 2014
$1.5M
THERAPEUTIC ANGIOGENESIS IN VASCULAR MEDICINE IIR37HL053354 · NHLBI · CARITAS ST. ELIZABETH'S MEDICAL CENTER · PI ISNER, JEFFREY · 2000 to 2001
$726k
Ethanol mediated endothelial injury and dysfunctionR21AA014575 · NIAAA · STEWARD ST. ELIZABETH'S MEDICAL CENTER · PI KISHORE, RAJ · 2006 to 2007
$413k
NHLBI NIH HHS 1R01HL116729NHLBI NIH HHS HL053354NHLBI NIH HHS HL091983NHLBI NIH HHS HL108795NHLBI NIH HHS HL108806NHLBI NIH HHS P01 HL108795NHLBI NIH HHS P01 HL108806NHLBI NIH HHS R01 HL053354NHLBI NIH HHS R01 HL091983NHLBI NIH HHS R01 HL095874NHLBI NIH HHS R01 HL105597NHLBI NIH HHS R01 HL116729NHLBI NIH HHS R01 HL126186NHLBI NIH HHS R37 HL053354NIAAA NIH HHS R21 AA014575
6 · The paper itself

Abstract

backgroundMicroRNA (miR) dysregulation in the myocardium has been implicated in cardiac remodeling after injury or stress.

objectivesThe aim of this study was to explore the role of miR in human CD34(+) cell (hCD34(+)) dysfunction in vivo after transplantation into the myocardium under ischemia-reperfusion (I-R) conditions.

methodsIn response to inflammatory stimuli, the miR array profile of endothelial progenitor cells was analyzed using a polymerase chain reaction-based miR microarray. miR-377 expression was assessed in myocardial tissue from human patients with heart failure (HF). We investigated the effect of miR-377 inhibition on an hCD34(+) cell angiogenic proteome profile in vitro and on cardiac repair and function after I-R injury in immunodeficient mice.

resultsThe miR array data from endothelial progenitor cells in response to inflammatory stimuli indicated changes in numerous miR, with a robust decrease in the levels of miR-377. Human cardiac biopsies from patients with HF showed significant increases in miR-377 expression compared with nonfailing control hearts. The proteome profile of hCD34(+) cells transfected with miR-377 mimics showed significant decrease in the levels of proangiogenic proteins versus nonspecific control-transfected cells. We also validated that serine/threonine kinase 35 is a target of miR-377 using a dual luciferase reporter assay. In a mouse model of myocardial I-R, intramyocardial transplantation of miR-377 silenced hCD34(+) cells in immunodeficient mice, promoting neovascularization (at 28 days, post-I-R) and lower interstitial fibrosis, leading to improved left ventricular function.

conclusionsThese findings indicate that HF increased miR-377 expression in the myocardium, which is detrimental to stem cell function, and transplantation of miR-377 knockdown hCD34(+) cells into ischemic myocardium promoted their angiogenic ability, attenuating left ventricular remodeling and cardiac fibrosis.

Indexed as

AdultAnimalsAntigens, CD34Endothelial Progenitor CellsFemaleHeartHeart FailureHumansInflammationMaleMiceMice, Inbred C57BLMice, KnockoutMicroRNAsMyocardiumNeovascularization, PhysiologicAntigens, CD34MicroRNAsMIRN377 microRNA, humanendothelial progenitor cellsheart failureneovascularization

Identifiers

PMID26564600
PMCPMC4644493
OpenAlexW2131283387

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.