Evidence map›Paper›PMID 38688405›Full record

ArticleBiochimica et biophysica acta. Biomembranes2024

The molecular arrangement of ceramides in the unit cell of the long periodicity phase of stratum corneum models shows a high adaptability to different ceramide head group structures.

Andreea Nădăban, Gerrit S Gooris, Charlotte M Beddoes, Robert M Dalgliesh, Marc Malfois, Bruno Demé, Joke A Bouwstra

Abstract read
In one paragraph

Article in Biochimica et biophysica acta. Biomembranes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Andreea NădăbanDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, Einsteinweg 55, Leiden 2333CC, the Netherlands.
Gerrit S GoorisDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, Einsteinweg 55, Leiden 2333CC, the Netherlands.
Charlotte M BeddoesDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, Einsteinweg 55, Leiden 2333CC, the Netherlands.
Robert M DalglieshISIS Neutron and Muon Source, Science and Technology Facilities Council, Rutherford Appleton Laboratory, Harwell Oxford, Didcot OX11 0QX, United Kingdom.
Marc MalfoisALBA Synchrotron, Carrer de la Llum 2-6, Cerdanyola del Vallès 08290, Barcelona, Spain.
Bruno DeméInstitut Laue-Langevin, 38000 Grenoble, France.
Joke A BouwstraDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, Einsteinweg 55, Leiden 2333CC, the Netherlands. Electronic address: bouwstra@lacdr.leidenuniv.nl.

Funding

Insights into skin barrier function: In silico and experimental studies of healthy and diseased stratum corneum lipid modelsR01AR072679 · NIAMS · VANDERBILT UNIVERSITY · PI LAIBINIS, PAUL E · 2018 to 2022
$1.5M
NIAMS NIH HHS R01 AR072679
6 · The paper itself

Abstract

The stratum corneum (SC) lipid matrix, composed primarily of ceramides (CERs), cholesterol and free fatty acids (FFA), has an important role for the skin barrier function. The presence of the long periodicity phase (LPP), a unique lamellar phase, is characteristic for the SC. Insight into the lipid molecular arrangement within the LPP unit cell is imperative for understanding the relationship between the lipid subclasses and the skin barrier function. In this study, the impact of the CER head group structure on the lipid arrangement and barrier functionality was investigated using lipid models forming the LPP. The results demonstrate that the positions of CER N-(tetracosanoyl)-sphingosine (CER NS) and CER N-(tetracosanoyl)-phytosphingosine (CER NP), two essentials CER subclasses, are not influenced by the addition of another CER subclass (N-(tetracosanoyl)-dihydrosphingosine (CER NdS), N-(2R-hydroxy-tetracosanoyl)-sphingosine (CER AS) or D-(2R-hydroxy-tetracosanoyl)-phytosphingosine (CER AP)). However, differences are observed in the lipid organization and the hydrogen bonding network of the three different models. A similar localization of CER NP and CER NS is also observed in a more complex lipid model, with the CER subclass composition mimicking that of human SC. These studies show the adaptability and insensitivity of the LPP unit cell structure to changes in the lipid head group structures of the CER subclasses.

Indexed as

CeramidesEpidermisCholesterolHumansSphingosineCeramidesCholesterolphytosphingosineSphingosineBarrier functionCeramidesCholesterolFatty acidsLipidsSkin

Identifiers

PMID38688405
PMCPMC13366156

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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.