Evidence map›Paper›PMID 34768767›Full record

ReviewInternational journal of molecular sciences2021

Mitochondria as a Cellular Hub in Infection and Inflammation.

Pauline Andrieux, Christophe Chevillard, Edecio Cunha-Neto, João Paulo Silva Nunes

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 174 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
174citing papers in PubMed, 4 pooled it
–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

174 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
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  5. Article
  6. Review
  7. ProtectiveiScience · 2026
    Article
  8. Review
  9. Oxygen-vacancy-engineered t-ZnO-CeOBioactive materials · 2026
    Article
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114 more citing papers are in PubMed but not listed here.

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

4 authors.

Pauline AndrieuxInserm, INSERM, UMR_1090, Aix Marseille Université, TAGC Theories and Approaches of Genomic Complexity, Institut MarMaRa, 13288 Marseille, France.
Christophe ChevillardInserm, INSERM, UMR_1090, Aix Marseille Université, TAGC Theories and Approaches of Genomic Complexity, Institut MarMaRa, 13288 Marseille, France.ORCID 0000-0002-5269-8813
Edecio Cunha-NetoLaboratory of Immunology, Heart Institute (InCor), Division of Clinical Immunology and Allergy, School of Medicine, University of São Paulo, São Paulo 05403-000, Brazil.ORCID 0000-0002-3699-3345
João Paulo Silva NunesInserm, INSERM, UMR_1090, Aix Marseille Université, TAGC Theories and Approaches of Genomic Complexity, Institut MarMaRa, 13288 Marseille, France.

Funding

the Aix-Marseille University AMIDEX "International_2018" MITOMUTCHAGASthe CNPq (Brazilian Council for Scientific and Technological Development) nonethe Excellence Initiative of Aix-Marseille University - A*Midex Institute MarMaRa AMX-19-IET-007the FAPESP (São Paulo State Research Funding Agency Brazil) 2013/50302-3the FAPESP (São Paulo State Research Funding Agency Brazil) 2014/50890-5the French Agency for Research (Agence Nationale de la Recherche-ANR) Br-Fr-Chagasthe French Agency for Research (Agence Nationale de la Recherche-ANR) landscardiothe Inserm Cross-Cutting Project GOLD nonethe Institut National de la Santé et de la Recherche Médicale (INSERM) nonethe National Institutes of Health/USA 2 P50 AI098461-02the National Institutes of Health/USA 2U19AI098461-06
6 · The paper itself

Abstract

Mitochondria are the energy center of the cell. They are found in the cell cytoplasm as dynamic networks where they adapt energy production based on the cell's needs. They are also at the center of the proinflammatory response and have essential roles in the response against pathogenic infections. Mitochondria are a major site for production of Reactive Oxygen Species (ROS; or free radicals), which are essential to fight infection. However, excessive and uncontrolled production can become deleterious to the cell, leading to mitochondrial and tissue damage. Pathogens exploit the role of mitochondria during infection by affecting the oxidative phosphorylation mechanism (OXPHOS), mitochondrial network and disrupting the communication between the nucleus and the mitochondria. The role of mitochondria in these biological processes makes these organelle good targets for the development of therapeutic strategies. In this review, we presented a summary of the endosymbiotic origin of mitochondria and their involvement in the pathogen response, as well as the potential promising mitochondrial targets for the fight against infectious diseases and chronic inflammatory diseases.

Indexed as

AnimalsEnergy MetabolismHumansInfectionsInflammationMitochondriaMitochondrial Dynamicsinfectioninfection diseaseinflammationinflammatory diseasemitochondriamitochondria dysfunctionmitochondrial bioenergetics

Identifiers

PMID34768767
PMCPMC8583510

What Socratic 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 Socratic graph.