Evidence map›Paper›PMID 30155598›Full record

ArticleJournal of cardiovascular translational research2018

Exosome-Derived Dystrophin from Allograft Myogenic Progenitors Improves Cardiac Function in Duchenne Muscular Dystrophic Mice.

Xuan Su, Yue Jin, Yan Shen, Chengwei Ju, Jingwen Cai, Yutao Liu, Il-Man Kim, Yu Wang, Hong Yu, Neal L Weintraub and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cardiovascular translational research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  4. Enhanced secretion of promyogenic exosomes by quiescent muscle cells.Frontiers in cell and developmental biology · 2024
    Article
  5. Extracellular Vesicles for Muscle Atrophy Treatment.Advances in experimental medicine and biology · 2023
    Review
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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

12 authors at 4 institutions in 2 countries.

Xuan SuDepartment of Cardiology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, 160, Pujian Road, Shanghai, 200127, China.
Yue JinDepartment of Cardiology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, 160, Pujian Road, Shanghai, 200127, China.
Yan ShenVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA, 30912, USA.
Chengwei JuDepartment of Cardiology, Zhongda Hospital, Medical School of Southeast University, Nanjing, China.
Jingwen CaiVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA, 30912, USA.
Yutao LiuVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA, 30912, USA.
Il-Man KimVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA, 30912, USA.
Yu WangDepartment of Cardiology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, 160, Pujian Road, Shanghai, 200127, China.
Hong YuDepartment of Cardiology, Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, 310009, China.
Neal L WeintraubVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA, 30912, USA.
Meng JiangDepartment of Cardiology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, 160, Pujian Road, Shanghai, 200127, China. jiangmeng0919@163.com.
Yaoliang TangVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA, 30912, USA. yaotang@augusta.edu.ORCID 0000-0002-8372-1545
Augusta University · USRenji Hospital · CNSecond Affiliated Hospital of Zhejiang University · CNZhongda Hospital Southeast University · CN

Funding

Hypoxia and cardiac stem cell homingR01HL086555 · NHLBI · UNIVERSITY OF CINCINNATI · PI TANG, YAO LIANG · 2008 to 2019
$3.5M
Innovative Approaches to Treat Duchenne Muscular Dystrophy Using iPSC-Derived Muscle ProgenitorsR01AR070029 · NIAMS · AUGUSTA UNIVERSITY · PI ASHRAF, MUHAMMAD, TANG, YAO LIANG · 2016 to 2021
$2.6M
Notch1/miR-322 Axis in Stem Cell Mediated Vascular RepairR01HL134354 · NHLBI · AUGUSTA UNIVERSITY · PI ASHRAF, MUHAMMAD, TANG, YAO LIANG · 2016 to 2020
$2.5M
Beta-arrestin signaling and microRNA biogenesis in cardioprotectionR01HL124251 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI KIM, IL-MAN · 2014 to 2018
$1.9M
Epigenetic regulation of HDAC9 in obesity and atherosclerosisR01HL126949 · NHLBI · AUGUSTA UNIVERSITY · PI WEINTRAUB, NEAL L · 2016 to 2019
$1.8M
American Heart Association-American Stroke Association 18TPA34170104NHLBI NIH HHS R01 HL086555NHLBI NIH HHS R01 HL124251NHLBI NIH HHS R01 HL126949NHLBI NIH HHS R01 HL134354NIAMS NIH HHS R01 AR070029
6 · The paper itself

Abstract

Progressive cardiomyocyte loss in Duchenne muscular dystrophy (DMD) leads to cardiac fibrosis, cardiomyopathy, and eventually heart failure. In the present study, we observed that myogenic progenitor cells (MPC) carry mRNA for the dystrophin gene. We tested whether cardiac function can be improved in DMD by allograft transplantation of MPC-derived exosomes (MPC-Exo) into the heart to restore dystrophin protein expression. Exo from C2C12 cells (an MPC cell line) or vehicle were delivered locally into the hearts of MDX mice. After 2 days of treatment, we observed that MPC-Exo restored dystrophin expression in the hearts of MDX mice, which correlated with improved myocardial function in dystrophin-deficient MDX mouse hearts. In conclusion, this study demonstrated that allogeneic WT-MPC-Exo transplantation transiently restored dystrophin gene expression and improved cardiac function in MDX mice, suggesting that allogenic exosomal delivery may serve as an alternative treatment for cardiomyopathy of DMD.

Indexed as

Ventricular Function, LeftAllograftsAnimalsCardiomyopathiesCell LineDisease Models, AnimalDystrophinExosomesMaleMice, Inbred mdxMuscular Dystrophy, DuchenneMyoblastsMyocardiumRecovery of FunctionStem Cell Transplantationapo-dystrophin 1DystrophinCardiomyopathyDystrophinExosomeMyogenic progenitor cells

Identifiers

PMID30155598
PMCPMC6212302
OpenAlexW2889220630

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.