Effect of human cationic antimicrobial protein 18 Peptide on endotoxin-induced uveitis in rats.

Kazuhiro Ohgami, Iliyana Bozhidarova Ilieva, Kenji Shiratori, Emiko Isogai, Kazuhiko Yoshida, Satoshi Kotake, Tomomi Nishida, Nobuhisa Mizuki, Shigeaki Ohno
Author Information
  1. Kazuhiro Ohgami: Department of Ophthalmology and Visual Sciences, Hokkaido University Graduate School of Medicine, Sapporo, Japan. kohgami@med.hokudai.ac.jp

Abstract

PURPOSE: Human cationic antimicrobial protein 18 (hCAP18, 18 kDa) was originally identified in leukocytes on the basis of its antimicrobial activity. The peptide composed of the 27 C-terminal amino acids of hCAP18 (hCAP18(109-135)) binds lipopolysaccharide (LPS). The purpose of the present study was to investigate the effects of hCAP18 peptide on endotoxin-induced uveitis (EIU) in rats.
METHODS: EIU was induced by footpad injection of LPS. Each rat was injected intravenously with 1, 10, or 100 micro g hCAP18 peptide in 0.1 mL of PBS immediately after LPS injection in male Lewis rats. At 24 hours after LPS injection, enzyme-linked immunosorbent assay was performed to evaluate concentrations of protein, nitric oxide (NO), tumor necrosis factor (TNF)-alpha, prostaglandin (PG)-E2, interleukin (IL)-6, monocyte chemoattractant protein (MCP)-1 and macrophage inflammatory protein (MIP)-2 in aqueous humor. Also, EIU was evaluated by counting inflammatory cells in aqueous humor.
RESULTS: hCAP18 peptide at 10 and 100 micro g significantly suppressed an LPS-induced increase in the number of inflammatory cells and the levels of protein, NO, TNF-alpha, PGE2, MCP-1, and MIP-2. The anti-inflammatory effect of 10 micro g hCAP18 peptide was as strong as that of 100 micro g hCAP18 peptide. Treatment with 1 micro g hCAP18 peptide did not suppress EIU, compared with the LPS group.
CONCLUSIONS: The present results indicate that hCAP18 peptide suppresses development of EIU. A possible mechanism for the ocular anti-inflammatory effect of hCAP18 peptide is that it suppresses onset of LPS-triggered inflammatory reactions by binding directly to LPS.

MeSH Term

Animals
Antimicrobial Cationic Peptides
Aqueous Humor
Cathelicidins
Chemokine CCL2
Chemokine CXCL2
Dinoprostone
Disease Models, Animal
Erythrocyte Aggregation
Injections, Intravenous
Interleukin-6
Lipopolysaccharides
Male
Monokines
Nitric Oxide
Rats
Rats, Inbred Lew
Salmonella typhimurium
Tumor Necrosis Factor-alpha
Uveitis, Anterior

Chemicals

Antimicrobial Cationic Peptides
Cathelicidins
Chemokine CCL2
Chemokine CXCL2
Interleukin-6
Lipopolysaccharides
Monokines
Tumor Necrosis Factor-alpha
Nitric Oxide
Dinoprostone

Word Cloud

Created with Highcharts 10.0.0hCAP18peptideproteinLPSEIUmicroginflammatoryantimicrobial18ratsinjection110100cationicpresentendotoxin-induceduveitisNOaqueoushumorcellsanti-inflammatoryeffectsuppressesPURPOSE:HumankDaoriginallyidentifiedleukocytesbasisactivitycomposed27C-terminalaminoacids109-135bindslipopolysaccharidepurposestudyinvestigateeffectsMETHODS:inducedfootpadratinjectedintravenously0mLPBSimmediatelymaleLewis24hoursenzyme-linkedimmunosorbentassayperformedevaluateconcentrationsnitricoxidetumornecrosisfactorTNF-alphaprostaglandinPG-E2interleukinIL-6monocytechemoattractantMCP-1macrophageMIP-2AlsoevaluatedcountingRESULTS:significantlysuppressedLPS-inducedincreasenumberlevelsTNF-alphaPGE2MCP-1MIP-2strongTreatmentsuppresscomparedgroupCONCLUSIONS:resultsindicatedevelopmentpossiblemechanismocularonsetLPS-triggeredreactionsbindingdirectlyEffecthumanPeptide

Similar Articles

Cited By