Evidence map›Paper›PMID 41413833›Full record

ArticleCell communication and signaling : CCS2025

Mitochondria-derived vesicles serve as reactors in response to stress in cardiomyocytes.

Yiqing Zhou, Shi Jia, Yufei Xiong, Lebin Gan, Saifang Yan, Junhui Zhao, Minghong Leng, Fenghe Yang, Mingyang Zhao, Limei Liu and 3 more

Abstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Review
  2. Review
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

13 authors.

Yiqing Zhou *Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Peking University, Beijing, 100191, P.R. China.
Shi Jia *Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Peking University, Beijing, 100191, P.R. China.
Yufei XiongDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Peking University, Beijing, 100191, P.R. China.
Lebin GanKey Laboratory of Trauma Treatment and Neural Regeneration (Peking University), Trauma Treatment Center, National Center for Trauma Medicine, Peking University People's Hospital, Beijing, 100044, P.R. China.
Saifang YanDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Peking University, Beijing, 100191, P.R. China.
Junhui ZhaoDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Peking University, Beijing, 100191, P.R. China.
Minghong LengDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Peking University, Beijing, 100191, P.R. China.
Fenghe YangDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Peking University, Beijing, 100191, P.R. China.
Mingyang ZhaoDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Peking University, Beijing, 100191, P.R. China.
Limei LiuDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Peking University, Beijing, 100191, P.R. China.
Yangpo CaoDepartment of Pharmacology, School of Medicine, Southern University of Science and Technology, Shenzhen, China.
Jingjing YeKey Laboratory of Trauma Treatment and Neural Regeneration (Peking University), Trauma Treatment Center, National Center for Trauma Medicine, Peking University People's Hospital, Beijing, 100044, P.R. China. yejingjing@bjmu.edu.cn.
Ming ZhengDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Peking University, Beijing, 100191, P.R. China. zhengm@bjmu.edu.cn.

Funding

Beijing Tongzhou District Science and Technology Innovation Talent Outstanding Youth Project JCQN2024006National Key Research and Development Program of China 2020YFA0803802National Natural Science Foundation of China 31800974National Natural Science Foundation of China 81873457National Natural Science Foundation of China 82470247National Natural Science Foundation of China 82572864Natural Science Foundation of Beijing Municipality 7222193
6 · The paper itself

Abstract

backgroundMitochondria-derived vesicles (MDVs) are a novel type of mitochondrial quality control (MQC) found in different types of cells. Strictly-organized adult cardiomyocytes contain abundant mitochondria; however, the precise characteristics and functions of MDVs in the heart remain unclear.

methodsRat cardiomyocytes were examined using transmission electron microscopy (TEM) to visualize MDVs. Live-cell imaging with STED microscopy and fluorescent mitochondrial dyes (PK Mito Red and PK Mito Deep Red) was performed to track MDV dynamics in neonatal and adult rat cardiomyocytes. Nanoparticle tracking analysis (NTA) was used to assess the size and quantity of MDVs. MDVs were purified from heart mitochondria, and their protein profile was analyzed by proteomics. RNA sequencing was conducted on neonatal cardiomyocytes treated with MDVs to explore transcriptomic changes.

resultsMDVs were observed in live rat cardiomyocytes with TEM revealing vesicles 70-150 nm in diameter. MDVs were universally distributed, showed active motility, and colocalized with other intracellular organelles in adult cardiomyocytes. Proteomics analysis showed MDV-associated proteins and found that the respiratory functions of MDVs were preserved in cardiomyocytes. The number of MDVs in cardiomyocytes was found to increase in response to various acute physiological and pathological stimuli. By increasing the number of MDVs in cardiomyocytes with exogenously purified myocardial MDVs and analyzing transcriptomic changes via RNA sequencing, we found that a greater number of MDVs in cardiomyocytes altered genes in stress-related signaling pathways.

conclusionMDVs in cardiomyocytes colocalize with other organelles, which might facilitate inter-organelle communication, and serve as reactors in response to stress in adult cardiomyocytes.

Indexed as

MitochondriaMitochondria, HeartMyocytes, CardiacStress, PhysiologicalAnimalsProteomicsRatsRats, Sprague-DawleyAdult cardiomyocyteInter-organelle communicationMDVsMitochondrial dynamicsResponse to stress

Identifiers

PMID41413833
PMCPMC12825251

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.