Evidence map›Paper›PMID 31593566›Full record

ArticlePLoS biology2019

Cisd2 is essential to delaying cardiac aging and to maintaining heart functions.

Chi-Hsiao Yeh, Zhao-Qing Shen, Shao-Yu Hsiung, Pei-Chun Wu, Yuan-Chi Teng, Yi-Ju Chou, Su-Wen Fang, Chian-Feng Chen, Yu-Ting Yan, Lung-Sen Kao and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 55 citations in OpenAlex.

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  9. CISD3/MiNT is required for complex I function, mitochondrial integrity, and skeletal muscle maintenance.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  14. Rejuvenation: Turning Back Time by Enhancing CISD2.International journal of molecular sciences · 2022
    Review
  15. Review
  16. Article
  17. Article
  18. Dysregulated CaCells · 2022
    Review
  19. Article
  20. Article
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 1 country.

Chi-Hsiao YehDepartment of Thoracic and Cardiovascular Surgery, Chang Gung Memorial Hospital, Keelung, Taiwan.ORCID 0000-0002-8850-4144
Zhao-Qing ShenDepartment of Life Sciences and Institute of Genome Sciences, National Yang-Ming University, Taipei, Taiwan.
Shao-Yu HsiungProgram in Molecular Medicine, School of Life Sciences, National Yang-Ming University and Academia Sinica, Taipei, Taiwan.ORCID 0000-0002-3776-0623
Pei-Chun WuBrain Research Center, National Yang-Ming University, Taipei, Taiwan.
Yuan-Chi TengDepartment of Life Sciences and Institute of Genome Sciences, National Yang-Ming University, Taipei, Taiwan.ORCID 0000-0002-0372-6734
Yi-Ju ChouProgram in Molecular Medicine, School of Life Sciences, National Yang-Ming University and Academia Sinica, Taipei, Taiwan.
Su-Wen FangDepartment of Thoracic and Cardiovascular Surgery, Chang Gung Memorial Hospital, Keelung, Taiwan.
Chian-Feng ChenGenome Research Center, National Yang-Ming University, Taipei, Taiwan.ORCID 0000-0002-4906-7949
Yu-Ting YanInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Lung-Sen KaoDepartment of Life Sciences and Institute of Genome Sciences, National Yang-Ming University, Taipei, Taiwan.
Cheng-Heng KaoCenter of General Education, Chang Gung University, Taoyuan, Taiwan.
Ting-Fen TsaiDepartment of Life Sciences and Institute of Genome Sciences, National Yang-Ming University, Taipei, Taiwan.
National Yang Ming Chiao Tung University · TWChang Gung University · TWInstitute of Biomedical Sciences, Academia Sinica · TWKeelung Chang Gung Memorial Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CDGSH iron-sulfur domain-containing protein 2 (Cisd2) is pivotal to mitochondrial integrity and intracellular Ca2+ homeostasis. In the heart of Cisd2 knockout mice, Cisd2 deficiency causes intercalated disc defects and leads to degeneration of the mitochondria and sarcomeres, thereby impairing its electromechanical functioning. Furthermore, Cisd2 deficiency disrupts Ca2+ homeostasis via dysregulation of sarco/endoplasmic reticulum Ca2+-ATPase (Serca2a) activity, resulting in an increased level of basal cytosolic Ca2+ and mitochondrial Ca2+ overload in cardiomyocytes. Most strikingly, in Cisd2 transgenic mice, a persistently high level of Cisd2 is sufficient to delay cardiac aging and attenuate age-related structural defects and functional decline. In addition, it results in a younger cardiac transcriptome pattern during old age. Our findings indicate that Cisd2 plays an essential role in cardiac aging and in the heart's electromechanical functioning. They highlight Cisd2 as a novel drug target when developing therapies to delay cardiac aging and ameliorate age-related cardiac dysfunction.

Indexed as

AgingAging, PrematureAnimalsAtrioventricular BlockAutophagy-Related ProteinsCalciumElectrocardiographyGene Expression ProfilingGene Expression RegulationHeartHomeostasisMaleMiceMice, KnockoutMitochondria, HeartMyocytes, CardiacAutophagy-Related ProteinsCalciumNerve Tissue ProteinsNoxp70 protein, mouseSarcoplasmic Reticulum Calcium-Transporting ATPases

Identifiers

PMID31593566
PMCPMC6799937
OpenAlexW2979435734

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.