Evidence map›Paper›PMID 31118291›Full record

ArticleScience translational medicine2019

Circulating exosomes derived from transplanted progenitor cells aid the functional recovery of ischemic myocardium.

Progyaparamita Saha, Sudhish Sharma, Laxminarayana Korutla, Srinivasa Raju Datla, Farnaz Shoja-Taheri, Rachana Mishra, Grace E Bigham, Malini Sarkar, David Morales, Gregory Bittle and 11 more

Open access · greenAbstract read
In one paragraph

Article in Science translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

60 citing papers in PubMed, 94 citations in OpenAlex.

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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

21 authors at 3 institutions in 1 country.

Progyaparamita SahaDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.ORCID 0000-0002-0248-3531
Sudhish SharmaDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Laxminarayana KorutlaDivision of Cardiovascular Surgery, University of Pennsylvania, Philadelphia, PA 19104, USA.
Srinivasa Raju DatlaDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Farnaz Shoja-TaheriWallace H. Coulter Department of Biomedical Engineering and Division of Cardiology, Emory University School of Medicine, Atlanta, GA 30322, USA.ORCID 0000-0003-3939-6674
Rachana MishraDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Grace E BighamDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Malini SarkarDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.ORCID 0000-0003-1013-5841
David MoralesDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.ORCID 0000-0003-3751-4614
Gregory BittleDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Muthukumar GunasekaranDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Chetan AmbasthaDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Mir Yasir ArfatDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Deqiang LiDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Andreas HabertheuerDivision of Cardiovascular Surgery, University of Pennsylvania, Philadelphia, PA 19104, USA.
Robert HuDivision of Cardiovascular Surgery, University of Pennsylvania, Philadelphia, PA 19104, USA.
Manu O PlattWallace H. Coulter Department of Biomedical Engineering and Division of Cardiology, Emory University School of Medicine, Atlanta, GA 30322, USA.ORCID 0000-0001-6390-4320
Peixin YangDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Michael E DavisWallace H. Coulter Department of Biomedical Engineering and Division of Cardiology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Prashanth VallabhajosyulaDivision of Cardiovascular Surgery, University of Pennsylvania, Philadelphia, PA 19104, USA. skaushal@smail.umaryland.edu prashanth.vallabhajosyula@uphs.upenn.edu.
Sunjay KaushalDivision of Cardiovascular Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA. skaushal@smail.umaryland.edu prashanth.vallabhajosyula@uphs.upenn.edu.ORCID 0000-0002-0511-9997
University of Maryland, Baltimore · USUniversity of Pennsylvania · USThe Wallace H. Coulter Department of Biomedical Engineering · US

Funding

Interdisciplinary Training Program Muscle BiologyT32AR007592 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Aikaterini Kontrogianni-Konstantopoulos · 1996 to 2026
$11.7M
Mechanism of transplanted neonatal cardiac progenitor cells to repair ischemic myocardiumR01HL118491 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI SCHUMACKER, PAUL T · 2014 to 2024
$4.4M
Predictive and systems modeling of exosome cargoR01HL145644 · NHLBI · EMORY UNIVERSITY · PI DAVIS, MICHAEL E · 2019 to 2022
$3.1M
Characterization of the Cardiac Progenitor Cell Exosomes for Optimal TherapeuticsR01HL141922 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI KAUSHAL, SUNJAY · 2019 to 2022
$2.8M
MicroRNA-Suppressed Mitochondrial Fusion in Mediating the Teratogenicity of Maternal Diabetes Leading to Heart DefectsR01HL134368 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI WANG, JIAN-YING, YANG, PEIXIN · 2017 to 2020
$2.4M
The Role of C-Kit Positive Cardiac Progenitors in Maternal Diabetes-Induced Heart Defects and the Therapeutic Values of These CellsR01HL139060 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI KAUSHAL, SUNJAY, YANG, PEIXIN · 2017 to 2020
$2.4M
NHLBI NIH HHS R01 HL118491NHLBI NIH HHS R01 HL139060NHLBI NIH HHS R01 HL141922NHLBI NIH HHS R01 HL145644NIAMS NIH HHS T32 AR007592
6 · The paper itself

Abstract

The stem cell field is hindered by its inability to noninvasively monitor transplanted cells within the target organ in a repeatable, time-sensitive, and condition-specific manner. We hypothesized that quantifying and characterizing transplanted cell-derived exosomes in the recipient plasma would enable reliable, noninvasive surveillance of the conditional activity of the transplanted cells. To test this hypothesis, we used a human-into-rat xenogeneic myocardial infarction model comparing two well-studied progenitor cell types: cardiosphere-derived cells (CDCs) and c-kit

Indexed as

Recovery of FunctionStem Cell TransplantationAgedAnimalsExosomesFemaleHumansMajor Histocompatibility ComplexMaleMicroRNAsMyocardial IschemiaMyocytes, CardiacPhenotypeProto-Oncogene Proteins c-kitRats, NudeReproducibility of ResultsMicroRNAsProto-Oncogene Proteins c-kit

Identifiers

PMID31118291
PMCPMC6857931
OpenAlexW2945889684

What OpenQuestion holds

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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.