Evidence map›Paper›PMID 34495738›Full record

ArticleMolecular biology of the cell2021

Discovery of bactericides as an acute mitochondrial membrane damage inducer.

Ryan Houston, Yusuke Sekine, Mads B Larsen, Kei Murakami, Steven J Mullett, Stacy G Wendell, Derek P Narendra, Bill B Chen, Shiori Sekine

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Antifungal Mechanism of Phenazine-1-Carboxylic Acid againstInternational journal of molecular sciences · 2023
    Article
  4. Article
  5. Article
  6. 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

9 authors.

Ryan HoustonAging Institute, Department of Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15219.
Yusuke SekineAging Institute, Department of Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15219.
Mads B LarsenAging Institute, Department of Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15219.
Kei MurakamiDepartment of Chemistry, School of Science, Kwansei Gakuin University, Sanda, Hyogo, Japan.
Steven J MullettDepartment of Pharmacology and Chemical Biology, the Health Sciences Metabolomics and Lipidomics Core, University of Pittsburgh, Pittsburgh, PA 15261.
Stacy G WendellDepartment of Pharmacology and Chemical Biology, the Health Sciences Metabolomics and Lipidomics Core, University of Pittsburgh, Pittsburgh, PA 15261.
Derek P NarendraInherited Movement Disorders Unit, Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892.
Bill B ChenAging Institute, Department of Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15219.
Shiori SekineAging Institute, Department of Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15219.

Funding

Systematic Investigation of Protein Ubiquitination in ARDSR35HL139860 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHEN, BEIBEI · 2018 to 2024
$6.3M
Bringing Untargeted Metabolomics to PittS10OD023402 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GELHAUS, STACY LYNN · 2018 to 2018
$594k
NHLBI NIH HHS R35 HL139860NIH HHS S10 OD023402
6 · The paper itself

Abstract

Mitochondria evolved from endosymbiotic bacteria to become essential organelles of eukaryotic cells. The unique lipid composition and structure of mitochondrial membranes are critical for the proper functioning of mitochondria. However, stress responses that help maintain the mitochondrial membrane integrity are not well understood. One reason for this lack of insight is the absence of efficient tools to specifically damage mitochondrial membranes. Here, through a compound screen, we found that two bis-biguanide compounds, chlorhexidine and alexidine, modified the activity of the inner mitochondrial membrane (IMM)-resident protease OMA1 by altering the integrity of the IMM. These compounds are well-known bactericides whose mechanism of action has centered on their damage-inducing activity on bacterial membranes. We found alexidine binds to the IMM likely through the electrostatic interaction driven by the membrane potential as well as an affinity for anionic phospholipids. Electron microscopic analysis revealed that alexidine severely perturbated the cristae structure. Notably, alexidine evoked a specific transcriptional/proteostasis signature that was not induced by other typical mitochondrial stressors, highlighting the unique property of alexidine as a novel mitochondrial membrane stressor. Our findings provide a chemical-biological tool that should enable the delineation of mitochondrial stress-signaling pathways required to maintain the mitochondrial membrane homeostasis.

Indexed as

Anti-Bacterial AgentsBiguanidesChlorhexidineDrug Evaluation, PreclinicalHeLa CellsHomeostasisHumansMembranesMetalloendopeptidasesMitochondriaMitochondrial MembranesMitochondrial ProteinsPhospholipidsalexidineAnti-Bacterial AgentsBiguanidesChlorhexidineMetalloendopeptidasesMitochondrial Proteinsmolecule metalloprotease-related protein-1, humanPhospholipids

Identifiers

PMID34495738
PMCPMC8693957

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.