Evidence map›Paper›PMID 39707562›Full record

ArticleStem cell research & therapy2024

Small extracellular vesicles derived from umbilical cord mesenchymal stem cells alleviate radiation-induced cardiac organoid injury.

Hu Cao, Liang Yue, Jingyuan Shao, Fanxuan Kong, Shenghua Liu, Hongyu Huai, Zhichao He, Zhuang Mao, Yuefeng Yang, Yingxia Tan and 1 more

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

11 authors.

Hu Cao *Beijing Institute of Radiation Medicine, Beijing, 100850, China.
Liang Yue *Department of Stem Cell and Regenerative Medicine, Institute of Health Service and Transfusion Medicine, 27 Taiping Road, Beijing, 100850, P.R. China.
Jingyuan Shao *Beijing Institute of Radiation Medicine, Beijing, 100850, China.
Fanxuan KongPLA Strategic Support Force Characteristic Medical Center, Beijing, 100101, China.
Shenghua LiuState Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Hongyu HuaiState Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Zhichao HeBeijing Institute of Radiation Medicine, Beijing, 100850, China.
Zhuang MaoBeijing Institute of Radiation Medicine, Beijing, 100850, China.
Yuefeng YangDepartment of Experimental Medical Science, Ningbo No.2 Hospital, Ningbo, 315010, China.
Yingxia TanDepartment of Stem Cell and Regenerative Medicine, Institute of Health Service and Transfusion Medicine, 27 Taiping Road, Beijing, 100850, P.R. China. tanhu333@126.com.
Hua WangBeijing Institute of Radiation Medicine, Beijing, 100850, China. 18511712135@163.com.ORCID 0000-0002-5728-7714

Funding

Natural Science Foundation of Zhejiang Province LY19H160010
6 · The paper itself

Abstract

backgroundRadiation-induced heart disease (RIHD) is one of the most serious complications of radiation therapy (RT) for thoracic tumors, and new interventions are needed for its prevention and treatment. Small extracellular vesicles (sEVs) from stem cells have attracted much attention due to their ability to repair injury. However, the role of umbilical cord mesenchymal stem cell (UCMSC)-derived sEVs in protecting cardiac organoids from radiation-induced injury and the underlying mechanisms are largely unknown.

methodsA radiation-induced cardiac organoid injury model was established by using X-ray radiation, and the optimal radiation dose of 20 Gy was determined by live/dead staining. After radiation, the cardiac organoids were treated with sEVs derived from UCMSCs, and energy metabolism, calcium transient changes and the ultrastructure of the organoids were assessed through Seahorse analysis, optical mapping and transmission electron microscopy, respectively. Confocal microscopy was used to observe the changes in mitochondrial ROS and mitochondrial membrane potential (ΔΨm). Furthermore, real-time quantitative PCR was used to verify the RNA-seq results.

resultsAfter X-ray radiation, the mortality of cardiac organoids significantly increased, energy metabolism decreased, and calcium transients changed. We also observed that the mitochondrial structure of cardiac organoids was disrupted and that ΔΨm was decreased. These effects could be inhibited by sEVs treatment. sEVs may protect against radiation-induced cardiac organoid injury by regulating oxidative phosphorylation and the p53 signaling pathway.

conclusionsEVs derived from UCMSCs can be used as a potential therapeutic strategy for radiation-induced heart disease.

Indexed as

Extracellular VesiclesMesenchymal Stem CellsOrganoidsUmbilical CordAnimalsCalciumHumansMembrane Potential, MitochondrialMiceMyocytes, CardiacRadiation InjuriesReactive Oxygen SpeciesCalciumReactive Oxygen SpeciesCardiac organoidsMesenchymal stem cellsMitochondrial functionRadiation-induced heart diseaseSmall extracellular vesicles

Identifiers

PMID39707562
PMCPMC11662859

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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.