Evidence map›Paper›PMID 27390127›Full record

ArticleThe EMBO journal2016

Macroautophagy inhibition maintains fragmented mitochondria to foster T cell receptor-dependent apoptosis.

Mauro Corrado, Francesca R Mariotti, Laura Trapani, Lucia Taraborrelli, Francesca Nazio, Valentina Cianfanelli, Maria Eugenia Soriano, Emilie Schrepfer, Francesco Cecconi, Luca Scorrano and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  3. Prostaglandin ENature communications · 2024
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  7. Article
  8. Targeting memory T cell metabolism to improve immunity.The Journal of clinical investigation · 2022
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Mitochondrial regulation of diabetic vascular disease: an emerging opportunity.Translational research : the journal of laboratory and clinical medicine · 2018
    Review
  17. Review
  18. Article
  19. Article
  20. 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

11 authors at 6 institutions in 3 countries.

Mauro CorradoDulbecco-Telethon Institute, Venetian Institute of Molecular Medicine, Padova, Italy IRCCS Fondazione Santa Lucia, Rome, Italy.
Francesca R MariottiIRCCS Fondazione Santa Lucia, Rome, Italy.
Laura TrapaniIRCCS Fondazione Santa Lucia, Rome, Italy.
Lucia TaraborrelliCentre for Cell Death, Cancer, and Inflammation (CCCI), UCL Cancer Institute, University College London, London, UK.
Francesca NazioDepartment of Pediatric Hematology and Oncology, IRCCS Bambino Gesù Children's Hospital, Rome, Italy Department of Biology, University of Rome Tor Vergata, Rome, Italy.
Valentina CianfanelliUnit of Cell Stress and Survival, Danish Cancer Society Research Center, Copenhagen, Denmark.
Maria Eugenia SorianoDepartment of Biology, University of Padova, Padova, Italy.
Emilie SchrepferDulbecco-Telethon Institute, Venetian Institute of Molecular Medicine, Padova, Italy Department of Biology, University of Padova, Padova, Italy.
Francesco CecconiIRCCS Fondazione Santa Lucia, Rome, Italy Department of Biology, University of Rome Tor Vergata, Rome, Italy Unit of Cell Stress and Survival, Danish Cancer Society Research Center, Copenhagen, Denmark.
Luca ScorranoDulbecco-Telethon Institute, Venetian Institute of Molecular Medicine, Padova, Italy Department of Biology, University of Padova, Padova, Italy.ORCID 0000-0002-8515-8928
Silvia CampelloIRCCS Fondazione Santa Lucia, Rome, Italy Department of Biology, University of Rome Tor Vergata, Rome, Italy silvia.campello@uniroma2.it.ORCID 0000-0003-0536-2484
University of Padua · ITUniversity of Rome Tor Vergata · ITFondazione Santa Lucia · ITCRUK Lung Cancer Centre of Excellence · GBDanish Cancer Society · DKVeneto Institute of Molecular Medicine · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial dynamics and functionality are linked to the autophagic degradative pathway under several stress conditions. However, the interplay between mitochondria and autophagy upon cell death signalling remains unclear. The T-cell receptor pathway signals the so-called activation-induced cell death (AICD) essential for immune tolerance regulation. Here, we show that this apoptotic pathway requires the inhibition of macroautophagy. Protein kinase-A activation downstream of T-cell receptor signalling inhibits macroautophagy upon AICD induction. This leads to the accumulation of damaged mitochondria, which are fragmented, display remodelled cristae and release cytochrome c, thereby driving apoptosis. Autophagy-forced reactivation that clears the Parkin-decorated mitochondria is as effective in inhibiting apoptosis as genetic interference with cristae remodelling and cytochrome c release. Thus, upon AICD induction regulation of macroautophagy, rather than selective mitophagy, ensures apoptotic progression.

Indexed as

ApoptosisAutophagyAnimalsCells, CulturedCytochromes cHumansMice, Inbred C57BLMitochondriaReceptors, Antigen, T-CellSignal TransductionT-LymphocytesCytochromes cReceptors, Antigen, T-CellAICDautophagymitochondrial dynamicsT cells

Identifiers

PMID27390127
PMCPMC5010050
OpenAlexW2462848035

What OpenQuestion holds

Textmetadata
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.