Evidence map›Paper›PMID 27136357›Full record

ArticlePloS one2016

Akap1 Deficiency Promotes Mitochondrial Aberrations and Exacerbates Cardiac Injury Following Permanent Coronary Ligation via Enhanced Mitophagy and Apoptosis.

Gabriele Giacomo Schiattarella, Fabio Cattaneo, Gianluigi Pironti, Fabio Magliulo, Giuseppe Carotenuto, Marinella Pirozzi, Roman Polishchuk, Domenica Borzacchiello, Roberta Paolillo, Marco Oliveti and 9 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
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  3. Article
  4. Review
  5. Mitochondrial Kinase Signaling for Cardioprotection.International journal of molecular sciences · 2024
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Mitochondrial ProteinFrontiers in pharmacology · 2022
    Article
  12. Article
  13. Article
  14. Review
  15. Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Article
  16. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 5 institutions in 3 countries.

Gabriele Giacomo SchiattarellaDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Fabio CattaneoDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Gianluigi PirontiDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Fabio MagliuloDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Giuseppe CarotenutoDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Marinella PirozziInstitute of Protein Biochemistry, Italian National Research Council (CNR-IBP), Naples, Italy.
Roman PolishchukTelethon Institute of Genetic and Medicine (TIGEM), Naples, Italy.
Domenica BorzacchielloDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Roberta PaolilloDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Marco OlivetiDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Nicola BoccellaDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Marisa AvvedimentoDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Maria SepeDepartment of Molecular Medicine and Medical Biotechnologies, Federico II University, Naples, Italy.
Assunta LombardiDepartment of Biology, Federico II University, Naples, Italy.
Rosa Anna BusielloDepartment of Biology, Federico II University, Naples, Italy.
Bruno TrimarcoDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Giovanni EspositoDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Antonio FelicielloDepartment of Molecular Medicine and Medical Biotechnologies, Federico II University, Naples, Italy.
Cinzia PerrinoDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Federico II University Hospital · ITKarolinska Institutet · SENational Research Council · ITTelethon Institute Of Genetics And Medicine · ITThe University of Texas Southwestern Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A-kinase anchoring proteins (AKAPs) transmit signals cues from seven-transmembrane receptors to specific sub-cellular locations. Mitochondrial AKAPs encoded by the Akap1 gene have been shown to modulate mitochondrial function and reactive oxygen species (ROS) production in the heart. Under conditions of hypoxia, mitochondrial AKAP121 undergoes proteolytic degradation mediated, at least in part, by the E3 ubiquitin ligase Seven In-Absentia Homolog 2 (Siah2). In the present study we hypothesized that Akap1 might be crucial to preserve mitochondrial function and structure, and cardiac responses to myocardial ischemia. To test this, eight-week-old Akap1 knockout mice (Akap1-/-), Siah2 knockout mice (Siah2-/-) or their wild-type (wt) littermates underwent myocardial infarction (MI) by permanent left coronary artery ligation. Age and gender matched mice of either genotype underwent a left thoracotomy without coronary ligation and were used as controls (sham). Twenty-four hours after coronary ligation, Akap1-/- mice displayed larger infarct size compared to Siah2-/- or wt mice. One week after MI, cardiac function and survival were also significantly reduced in Akap1-/- mice, while cardiac fibrosis was significantly increased. Akap1 deletion was associated with remarkable mitochondrial structural abnormalities at electron microscopy, increased ROS production and reduced mitochondrial function after MI. These alterations were associated with enhanced cardiac mitophagy and apoptosis. Autophagy inhibition by 3-methyladenine significantly reduced apoptosis and ameliorated cardiac dysfunction following MI in Akap1-/- mice. These results demonstrate that Akap1 deficiency promotes cardiac mitochondrial aberrations and mitophagy, enhancing infarct size, pathological cardiac remodeling and mortality under ischemic conditions. Thus, mitochondrial AKAPs might represent important players in the development of post-ischemic cardiac remodeling and novel therapeutic targets.

Indexed as

AdenineA Kinase Anchor ProteinsAnimalsApoptosisBlotting, WesternDisease Models, AnimalEchocardiographyIn Situ Nick-End LabelingMiceMice, KnockoutMicroscopy, ElectronMitochondriaMitophagyMyocardial InfarctionReactive Oxygen SpeciesUbiquitin-Protein Ligases3-methyladenineAdenineAkap1 protein, mouseA Kinase Anchor ProteinsReactive Oxygen SpeciesSiah2 protein, mouseUbiquitin-Protein Ligases

Identifiers

PMID27136357
PMCPMC4852950
OpenAlexW2345556940

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Registered trials

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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.