Cited by 63Antimicrobial Peptides and ActivitiesWound Healing and TreatmentsSkin and Cellular Biology Research

Differential expression of antimicrobial peptides in margins of chronic wounds

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Dressel, Stefanie, Harder, Jürgen, Cordes, Jesko, Wittersheim, Maike, Meyer‐Hoffert, Ulf, Sunderkötter, Cord, Gläser, Regine·2010·Experimental Dermatology

Abstract

Please cite this paper as: Differential expression of antimicrobial peptides in margins of chronic wounds. Experimental Dermatology 2010; 19: 628–632. Abstract: Skin wounds usually heal without major infections, although the loss of the mechanical epithelial barrier exposes the tissue to various bacteria. One reason may be the expression of antimicrobial peptides (AMP) of which some [human β‐defensins (hBD) and LL‐37] were recently shown to support additionally certain steps of wound healing. There are no studies which have compared expression patterns of different classes of AMP in chronic wounds. The aim of our study was therefore to analyse the expression profile of hBD‐2, hBD‐3, LL‐37, psoriasin and RNase 7 by immunohistochemistry from defined wound margins of chronic venous ulcers. We detected a strong induction of psoriasin and hBD‐2 in chronic wounds in comparison with healthy skin. Except for stratum corneum, no expression of RNase 7 and LL‐37 was detected in the epidermis while expression of hBD‐3 was heterogeneous. Bacterial swabs identified Staphylococcus aureus and additional bacterial populations, but no association between colonization and AMP expression was found. The differential expression of AMP is noteworthy considering the high bacterial load of chronic ulcers. Clinically, supplementation of AMP with the capability to enhance wound healing besides restricting bacterial overgrowth could present a physiological support for treatment of disturbed wound healing.

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Crossref · 10.1111/j.1600-0625.2009.01030.x

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  • In contrast, expression of other AMPs, such as S100A7, ribonuclease 7, hBD2, and hBD3, is not reduced in chronic wounds, but remains unchanged or is upregulated.

    “In contrast, expression of other AMPs, such as S100A7, ribonuclease 7 (RNase7), hBD2, and hBD3, is not reduced in chronic wounds, but remains unchanged or is upregulated.44”

    From The Innate Immune System in Acute and Chronic Wounds (2016) · cites this paper as [44]

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Authors
Dressel, S., Harder, J., Cordes, J., Wittersheim, M., Meyer‐Hoffert, U., Sunderkötter, C., & Gläser, R.
Affiliations
  • University Hospital Schleswig-Holstein (DE)
  • University of Münster (DE)
Corresponding author
Sunderkötter, Cord
Venue
Experimental Dermatology
Publisher
Wiley
Published
2010-06-14
Volume
19
Issue
7
Pages
628-632
ISSN
  • 0906-6705 (ISSN-L)
  • 1600-0625
OpenAlex
W1801159412
Cited by
63
References
23
Citations by year
2025: 2 · 2024: 1 · 2023: 1 · 2022: 1 · 2021: 3 · 2020: 3 · 2019: 2 · 2018: 2 · 2017: 4 · 2016: 5 · 2015: 4 · 2014: 7 · 2013: 7 · 2012: 5
FWCI
8.22
Type
journal article
Language
en
Open access
Locations
  • Experimental Dermatology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Immunology and Microbiology › Microbiology › Antimicrobial Peptides and Activities
  • Health Sciences › Medicine › Rehabilitation › Wound Healing and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Skin and Cellular Biology Research
Keywords
antimicrobial peptides, chronic wounds, venous leg ulcers, wound margin, human beta-defensins, human beta-defensin 2, human beta-defensin 3, LL-37, psoriasin, RNase 7, Staphylococcus aureus, bacterial colonization, wound healing, epidermis
MeSH terms
S100 Calcium Binding Protein A7, Aged, Humans, Immunohistochemistry, Male, Middle Aged, S100 Proteins, Ribonucleases, Staphylococcal Skin Infections, Varicose Ulcer, Wounds and Injuries, Gene Expression Profiling, beta-Defensins, Antimicrobial Cationic Peptides, Cathelicidins

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