Evidence map›Paper›PMID 39000442›Full record

ArticleInternational journal of molecular sciences2024

The Antimicrobial Activity of Human Defensins at Physiological Non-Permeabilizing Concentrations Is Caused by the Inhibition of the Plasma Membrane H

María T Andrés, Patricia Fierro, Victoria Antuña, José F Fierro

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. 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. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
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.

María T AndrésLaboratory of Oral Microbiology (LMO), University Clinic of Dentistry (CLUO), University of Oviedo, 33006 Oviedo, Asturias, Spain.ORCID 0000-0002-7827-981X
Patricia FierroLaboratory of Oral Microbiology (LMO), University Clinic of Dentistry (CLUO), University of Oviedo, 33006 Oviedo, Asturias, Spain.
Victoria AntuñaLaboratory of Oral Microbiology (LMO), University Clinic of Dentistry (CLUO), University of Oviedo, 33006 Oviedo, Asturias, Spain.
José F FierroLaboratory of Oral Microbiology (LMO), University Clinic of Dentistry (CLUO), University of Oviedo, 33006 Oviedo, Asturias, Spain.ORCID 0000-0003-2752-0690

Funding

Servicio para el Control de la Esterilización (SCE)/Laboratorio de Microbiología Oral (LMO) of the University of Oviedo, and the Fundación Sira Carrasco para la Ayuda a la Fibrosis Quística FUO-19-258, FUO-21-304, SV-03-FSCARRASCO
6 · The paper itself

Abstract

Human defensins are cysteine-rich peptides (Cys-rich peptides) of the innate immune system. Defensins contain an ancestral structural motif (i.e., γ-core motif) associated with the antimicrobial activity of natural Cys-rich peptides. In this study, low concentrations of human α- and β-defensins showed microbicidal activity that was not associated with cell membrane permeabilization. The cell death pathway was similar to that previously described for human lactoferrin, also an immunoprotein containing a γ-core motif. The common features were (1) cell death not related to plasma membrane (PM) disruption, (2) the inhibition of microbicidal activity via extracellular potassium, (3) the influence of cellular respiration on microbicidal activity, and (4) the influence of intracellular pH on bactericidal activity. In addition, in yeast, we also observed (1) partial K

Indexed as

Cell MembraneProton-Translocating ATPasesAnti-Infective Agentsbeta-DefensinsCandida albicansCell Membrane PermeabilityDefensinsHumansHydrogen-Ion ConcentrationLactoferrinMicrobial Sensitivity TestsPotassiumSaccharomyces cerevisiaeAnti-Infective Agentsbeta-DefensinsDefensinsLactoferrinPotassiumProton-Translocating ATPasesantimicrobial mechanism of actionantimicrobial peptidegamma-core motifH+-ATPasehBD-2hBD-3HNP-1HNP-4human defensinPma1p

Identifiers

PMID39000442
PMCPMC11242853

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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.