Evidence map›Paper›PMID 24732399›Full record

ArticleThe Journal of investigative dermatology2014

Basis for enhanced barrier function of pigmented skin.

Mao-Qiang Man, Tzu-Kai Lin, Juan L Santiago, Anna Celli, Lily Zhong, Zhi-Ming Huang, Truus Roelandt, Melanie Hupe, John P Sundberg, Kathleen A Silva and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 68 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Assessment of diaper dermatitis using a novel electronic health record-embedded scale.Journal of perinatology : official journal of the California Perinatal Association · 2024
    Article
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  19. Article
  20. Association between Stress and the HPA Axis in the Atopic Dermatitis.International journal of molecular sciences · 2017
    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

19 authors at 5 institutions in 4 countries.

Mao-Qiang ManDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA.
Tzu-Kai LinDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA; Graduate Institute of Clinical Medicine, National Cheng Kung University Medical College, Tainan, Taiwan; Department of Dermatology, National Cheng Kung University Medical College and Hospital, Tainan, Taiwan.
Juan L SantiagoDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA.
Anna CelliDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA.
Lily ZhongDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA.
Zhi-Ming HuangDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA.
Truus RoelandtDepartment of Dermatology, Universitair Ziekenhuis Brussel, Brussels, Belgium.
Melanie HupeDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA.
John P SundbergDepartment of Research and Development, The Jackson Laboratory, Bar Harbor, Maine, USA.
Kathleen A SilvaDepartment of Research and Development, The Jackson Laboratory, Bar Harbor, Maine, USA.
Debra CrumrineDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA.
Gemma Martin-EzquerraDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA; Department of Dermatology, Hospital del Mar-IMIM, Universitat Autonoma de Barcelona, Barcelona, Spain.
Carles TrullasISDIN, Research & Development, Barcelona, Spain.
Richard SunDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA.
Joan S WakefieldDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA.
Maria L WeiDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA.
Kenneth R FeingoldMedical Service, Department of Veterans Affairs Medical Center, and Department of Metabolism, University of California, San Francisco, San Francisco, California, USA.
Theodora M MauroDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA.
Peter M EliasDermatology Service, Department of Veterans Affairs Medical Center, San Francisco, California, USA; Department of Dermatology, University of California, San Francisco, San Francisco, California, USA. Electronic address: eliasp@derm.ucsf.edu.
San Francisco VA Medical Center · USJackson Laboratory · USIsdin (Spain) · ESUniversitair Ziekenhuis Brussel · BEUniversitat Autònoma de Barcelona · ES

Funding

NATURE OF THE MAMMALIAN CUTANEOUS PERMEABILITY BARRIERR01AR019098 · NIAMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI ELIAS, PETER M · 1986 to 2012
$4.2M
Aging Stratum Corneum pH and Barrier FunctionR01AG028492 · NIA · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI MAURO, THEODORA M · 2008 to 2012
$1.5M
NIAMS NIH HHS AR019098NIAMS NIH HHS R01 AR019098NIA NIH HHS AG028492NIA NIH HHS R01 AG028492
6 · The paper itself

Abstract

Humans with darkly pigmented skin display superior permeability barrier function in comparison with humans with lightly pigmented skin. The reduced pH of the stratum corneum (SC) of darkly pigmented skin could account for enhanced function, because acidifying lightly pigmented human SC resets barrier function to darkly pigmented levels. In SKH1 (nonpigmented) versus SKH2/J (pigmented) hairless mice, we evaluated how a pigment-dependent reduction in pH could influence epidermal barrier function. Permeability barrier homeostasis is enhanced in SKH2/J versus SKH1 mice, correlating with a reduced pH in the lower SC that colocalizes with the extrusion of melanin granules. Darkly pigmented human epidermis also shows substantial melanin extrusion in the outer epidermis. Both acute barrier disruption and topical basic pH challenges accelerate reacidification of SKH2/J (but not SKH1) SC, while inducing melanin extrusion. SKH2/J mice also display enhanced expression of the SC acidifying enzyme, secretory phospholipase A2f (sPLA2f). Enhanced barrier function of SKH2/J mice could be attributed to enhanced activity of two acidic pH-dependent, ceramide-generating enzymes, β-glucocerebrosidase and acidic sphingomyelinase, leading to accelerated maturation of SC lamellar bilayers. Finally, organotypic cultures of darkly pigmented human keratinocytes display enhanced barrier function in comparison with lightly pigmented cultures. Together, these results suggest that the superior barrier function of pigmented epidermis can be largely attributed to the pH-lowering impact of melanin persistence/extrusion and enhanced sPLA2f expression.

Indexed as

AcidsAnimalsCeramidesCytoplasmic GranulesEpidermal CellsEpidermisFemaleGlucosylceramidaseGroup II Phospholipases A2HomeostasisHumansHydrogen-Ion ConcentrationKeratinocytesLipid BilayersMaleMelaninsAcidsCeramidesGlucosylceramidaseGroup II Phospholipases A2Lipid BilayersMelaninsPla2g2f protein, mouseSphingomyelin Phosphodiesterase

Identifiers

PMID24732399
PMCPMC4134407
OpenAlexW2171728351

What OpenQuestion holds

Textmetadata
LicenceTDM
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.