Evidence map›Paper›PMID 23318173›Full record

ArticleBiochemical and biophysical research communications2013

Cardiac progenitor-derived exosomes protect ischemic myocardium from acute ischemia/reperfusion injury.

Lijuan Chen, Yingjie Wang, Yaohua Pan, Lan Zhang, Chengxing Shen, Gangjian Qin, Muhammad Ashraf, Neal Weintraub, Genshan Ma, Yaoliang Tang

Abstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 214 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
214citing papers in PubMed, 3 pooled it
12.3field-weighted citation impact, top 1% 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

214 citing papers in PubMed, 3 syntheses or guidelines pooled it, 348 citations in OpenAlex.

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154 more citing papers are in PubMed but not listed here.

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 5 institutions in 2 countries.

Lijuan ChenDepartment of Cardiology, Zhongda Hospital, Medical School of Southeast University, Nanjing 210009, China.
Yingjie Wang
Yaohua Pan
Lan Zhang
Chengxing Shen
Gangjian Qin
Muhammad Ashraf
Neal Weintraub
Genshan Ma
Yaoliang Tang
Sabin Vaccine Institute · USUniversity of Cincinnati · USNorthwestern University · USXinHua Hospital · CNZhongda Hospital Southeast University · CN

Funding

Vascular Protection During HypertensionP01HL062984 · NHLBI · UNIVERSITY OF IOWA · PI HEISTAD, DONALD D · 2000 to 2015
$22.2M
Hypoxia and cardiac stem cell homingR01HL086555 · NHLBI · UNIVERSITY OF CINCINNATI · PI TANG, YAO LIANG · 2008 to 2019
$3.5M
Angiotensin II, oxidative stress, and aneurysm formationR01HL076684 · NHLBI · UNIVERSITY OF IOWA · PI WEINTRAUB, NEAL L · 2005 to 2013
$3.0M
Perivascular adipose tissue and vascular remodelingR01HL112640 · NHLBI · UNIVERSITY OF CINCINNATI · PI WEINTRAUB, NEAL L · 2012 to 2016
$2.1M
NHLBI NIH HHS HL076684NHLBI NIH HHS HL086555NHLBI NIH HHS HL62984NHLBI NIH HHS P01 HL062984NHLBI NIH HHS R01 HL076684NHLBI NIH HHS R01 HL086555NHLBI NIH HHS R01 HL112640
6 · The paper itself

Abstract

backgroundCardiac progenitors (CPC) mediate cardioprotection via paracrine effects. To date, most of studies focused on secreted paracrine proteins. Here we investigated the CPC-derived-exosomes on protecting myocardium from acute ischemia/reperfusion (MI/R) injury. METHODS AND

resultsCPC were isolated from mouse heart using two-step protocol. Exosomes were purified from conditional medium, and confirmed by electron micrograph and Western blot using CD63 as a marker. qRT-PCR shows that CPC-exosomes have high level expression of GATA4-responsive-miR-451. Exosomes were ex vivo labeled with PKH26, We observed exosomes can be uptaken by H9C2 cardiomyoblasts with high efficiency after 12 h incubation. CPC-exosomes protect H9C2 from oxidative stress by inhibiting caspase 3/7 activation invitro. In vivo delivery of CPC-exosomes in an acute mouse myocardial ischemia/reperfusion model inhibited cardiomyocyte apoptosis by about 53% in comparison with PBS control (p<0.05).

conclusionOur results suggest, for the first time, the CPC-exosomes can be used as a therapeutic vehicle for cardioprotection, and highlights a new perspective for using non-cell exosomes for cardiac disease.

Indexed as

ExosomesAnimalsApoptosisDisease Models, AnimalMaleMiceMice, Inbred C57BLMyoblasts, CardiacMyocardial Reperfusion InjuryMyocardiumMyocytes, CardiacOxidative StressPolyethylene GlycolsPolyethylene Glycols

Identifiers

PMID23318173
PMCPMC3732190
OpenAlexW2170592926

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.