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Updated: Sep 29, 2026

Antimicrobial Peptides Produced by Selective Pressure Incorporation of Non-canonical Amino Acids
Published on: May 4, 2018
Antimicrobial peptides are expressed and produced in healthy and inflamed human synovial membranes
Friedrich Paulsen1, Thomas Pufe, Lenard Conradi
1Institute of Anatomy, Christian Albrecht University of Kiel, Germany. fpaulsen@anat.uni-kiel.de
Abstract:
The objective of this study was to determine the expression and production of antimicrobial peptides by healthy and inflamed human synovial membranes. Deposition of the antimicrobial peptides lysozyme, lactoferrin, secretory phospholipase A(2) (sPA(2)), matrilysin (MMP7), human neutrophil alpha-defensins 1-3 (HNP 1-3), human beta-defensin 1 (HBD-1), and human beta-defensin 2 (HBD-2) was determined by immunohistochemistry. Expression of mRNA for the antimicrobial peptides bactericidal permeability-increasing protein (BPI), heparin binding protein (CAP37), human cationic antimicrobial protein (LL37), human alpha-defensin 5 (HD5), human alpha-defensin 6 (HD6), HBD-1, HBD-2, and human beta-defensin 3 (HBD-3) was analysed by reverse transcription polymerase chain reaction (RT-PCR). RT-PCR revealed CAP37 and HBD-1 mRNA in samples of healthy synovial membrane. Additionally, HBD-3 and/or LL37 mRNA was detected in synovial membrane samples from patients with pyogenic arthritis (PA), osteoarthritis (OA) or rheumatoid arthritis (RA). BPI, HD5, HD6, and HBD-2 mRNAs were absent from all samples investigated. Immunohistochemistry identified lysozyme, lactoferrin, sPA(2), and MMP7 in type A synoviocytes of all samples. HBD-1 was only present in type B synoviocytes of some of the samples. Immunoreactive HBD-2 peptide was only visible in some inflamed samples. HNP1-3 was detected in both healthy and inflamed synovial membranes. The data suggest that human synovial membranes produce a broad spectrum of antimicrobial peptides. Under inflammatory conditions, the expression pattern changes, with induction of HBD-3 in PA (LL37 in RA; HBD-3 and LL37 in OA) as well as down-regulation of HBD-1. HBD-3 holds therapeutic potential in PA as it has a broad spectrum of antimicrobial activity and accelerates epithelial healing. However, caution is appropriate since defensins also promote fibrin formation and cell proliferation - key elements in joint infection. Clarification of the role of antimicrobial peptides in OA and RA will require further investigation.
Insights
Human synovial membranes produce various antimicrobial peptides, with expression patterns changing during inflammation. Human beta-defensin 3 shows therapeutic potential for pyogenic arthritis but requires further study.
Area of Science:
- Immunology
- Molecular Biology
- Rheumatology
Background:
- Human synovial membranes are crucial for joint health.
- Antimicrobial peptides (AMPs) play a role in innate immunity.
- Understanding AMPs in synovial inflammation is vital for treating joint diseases.
Purpose of the Study:
- To investigate the expression and production of AMPs in healthy and inflamed human synovial membranes.
- To identify specific AMPs present in synovial tissue and their changes during inflammation.
- To explore the potential therapeutic roles of identified AMPs.
Main Methods:
- Immunohistochemistry was used to detect AMP deposition.
- Reverse transcription polymerase chain reaction (RT-PCR) analyzed AMP mRNA expression.
- Synovial membrane samples from healthy individuals and patients with pyogenic arthritis, osteoarthritis, and rheumatoid arthritis were studied.
Main Results:
- Healthy synovial membranes expressed CAP37 and HBD-1 mRNA.
- Inflamed samples showed HBD-3 and/or LL37 mRNA, with distinct patterns in pyogenic arthritis, osteoarthritis, and rheumatoid arthritis.
- Lysozyme, lactoferrin, sPA(2), and MMP7 were found in synoviocytes; HNP1-3 was present in both healthy and inflamed tissues.
Conclusions:
- Human synovial membranes produce a diverse range of AMPs.
- Inflammation alters AMP expression, notably inducing HBD-3 and LL37 while down-regulating HBD-1.
- HBD-3 shows promise for pyogenic arthritis treatment, but its role in joint infections needs careful consideration.
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