Evidence map›Paper›PMID 31975567›Full record

ArticleJournal of cellular and molecular medicine2020

Notch1 protects against myocardial ischaemia-reperfusion injury via regulating mitochondrial fusion and function.

Shao-Hua Dai, Qi-Cai Wu, Rong-Rong Zhu, Xue-Mei Wan, Xue-Liang Zhou

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. MicroRNA-34a Promotes Ischemia-Induced Cardiomyocytes Apoptosis through Targeting Notch1.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  14. Mitochondrial Dynamics and Mitophagy in Cardiometabolic Disease.Frontiers in cardiovascular medicine · 2022
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Shao-Hua DaiDepartment of Cardiovascular Surgery, The First Affiliated Hospital, Nanchang University, Nanchang, 330006, China.ORCID 0000-0002-6836-4340
Qi-Cai WuDepartment of Cardiovascular Surgery, The First Affiliated Hospital, Nanchang University, Nanchang, 330006, China.
Rong-Rong ZhuDepartment of Obstetrics and Gynecology, High-tech hospital, The First Affiliated Hospital, Nanchang University, Nanchang, 330096, China.
Xue-Mei WanDepartment of Cardiovascular Surgery, The First Affiliated Hospital, Nanchang University, Nanchang, 330006, China.
Xue-Liang ZhouDepartment of Cardiovascular Surgery, The First Affiliated Hospital, Nanchang University, Nanchang, 330006, China.ORCID 0000-0003-2879-2882
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial fusion and fission dynamic are critical to the myocardial protection against ischaemia-reperfusion injury. Notch1 signalling plays an important role in heart development, maturation and repair. However, the role of Notch1 in the myocardial mitochondrial fusion and fission dynamic remains elusive. Here, we isolated myocardial cells from rats and established myocardial ischaemia-reperfusion injury (IRI) model. We modulated Notch1, MFN1 and DRP1 expression levels in myocardial cells via infection with recombinant adenoviruses. The results showed that Notch1 improves the cell viability and mitochondrial fusion in myocardiocytes exposed to IRI. These improvements were dependent on the regulation of MFN1 and DRP1. On the mechanism, we found that MNF1 is transcriptionally activated by RBP-Jk in myocardiocytes. Notch1 also improves the mitochondrial membrane potential in myocardiocytes exposed to IRI. Moreover, we further confirmed the protection of the Notch1-MFN1/Drp1 axis on the post-ischaemic recovery of myocardial performance is associated with the preservation of the mitochondrial structure. In conclusion, this study presented a detailed mechanism by which Notch1 signalling improves mitochondrial fusion during myocardial protection.

Indexed as

AnimalsApoptosisCell SurvivalDynaminsGene Expression RegulationGTP PhosphohydrolasesMaleMembrane Potential, MitochondrialMitochondria, HeartMitochondrial DynamicsMitochondrial Membrane Transport ProteinsMyocardial InfarctionMyocardial Reperfusion InjuryMyocardiumMyocytes, CardiacProtective AgentsDNM1L protein, humanDynaminsGTP PhosphohydrolasesMfn1 protein, humanMitochondrial Membrane Transport ProteinsNotch1 protein, ratProtective AgentsReceptor, Notch1DRP1MFN1mitochondrial fusionmyocardial ischaemic reperfusionNotch1

Identifiers

PMID31975567
PMCPMC7077547
OpenAlexW3003027173

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.