Granulocyte chemotactic protein 2 (gcp-2/cxcl6) complements interleukin-8 in periodontal disease

J Periodontal Res. 2009 Aug;44(4):465-71. doi: 10.1111/j.1600-0765.2008.01134.x. Epub 2008 Oct 7.

Abstract

Background and objective: Mucosal inflammatory responses are orchestrated largely by pro-inflammatory chemokines. The chemokine granulocyte chemotactic protein 2 (CXCL6) is involved in neutrophil recruitment and migration. Previous studies have shown that granulocyte chemotactic protein 2 is up-regulated during mucosal inflammation (e.g. in inflammatory bowel disease), similarly to the functionally and structurally related chemokine interleukin-8. Nevertheless, unlike interleukin-8, a role of granulocyte chemotactic protein 2 in gingival inflammation has not been yet demonstrated. In this study we aimed to evaluate the expression of the chemokine granulocyte chemotactic protein 2 in clinically healthy vs. diseased gingival tissues and to explore possible correlations with clinical and microbiological markers of periodontitis.

Material and methods: Gene expression in 184 'diseased' and 63 'healthy' gingival tissue specimens from 90 patients with periodontitis was analyzed using Affymetrix U133Plus2.0 arrays. The expression of granulocyte chemotactic protein 2 was further confirmed by real-time reverse transcription-polymerase chain reaction, western blotting and enzyme-linked immunosorbent assay, while the localization of granulocyte chemotactic protein 2 in gingival tissues was analyzed by immunohistochemistry. Plaque samples from the adjacent periodontal pockets were collected and evaluated for 11 species of periodontal bacteria using checkerboard DNA-DNA hybridizations.

Results: Among all known chemokines, GCP-2 expression was the most up-regulated (3.8-fold, p < 1.1 x 10(-16)), in 'diseased' vs. 'healthy' tissue as compared to a 2.6-fold increased expression of interleukin-8 mRNA (p < 1.2 x 10(-15)). Increased expression of granulocyte chemotactic protein 2 correlated with higher levels of 'red' and 'orange' complex pathogens and with increased probing depth, but not with attachment loss. Immunohistochemistry showed that granulocyte chemotactic protein 2 was expressed in gingival vascular endothelium.

Conclusion: The level of expression of granulocyte chemotactic protein 2 correlates with the severity of periodontitis and appears to act as a hitherto unrecognized functional adjunct to interleukin-8 in diseased gingival tissues.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actinomyces / immunology
  • Adolescent
  • Adult
  • Aged
  • Aggregatibacter actinomycetemcomitans / immunology
  • Aggressive Periodontitis / immunology*
  • Aggressive Periodontitis / microbiology
  • Bacteroides / immunology
  • Campylobacter rectus / immunology
  • Chemokine CXCL16
  • Chemokines, CXC / immunology*
  • Chronic Periodontitis / immunology*
  • Chronic Periodontitis / microbiology
  • Dental Plaque / microbiology
  • Eikenella corrodens / immunology
  • Endothelium, Vascular / immunology
  • Female
  • Fusobacterium nucleatum / immunology
  • Gingiva / blood supply
  • Gingiva / immunology
  • Humans
  • Inflammation Mediators / immunology
  • Interleukin-8 / immunology*
  • Male
  • Middle Aged
  • Periodontal Attachment Loss / immunology
  • Periodontal Attachment Loss / microbiology
  • Periodontal Pocket / immunology
  • Periodontal Pocket / microbiology
  • Porphyromonas gingivalis / immunology
  • Prevotella intermedia / immunology
  • Receptors, Scavenger / immunology*
  • Treponema denticola / immunology
  • Up-Regulation
  • Veillonella / immunology
  • Young Adult

Substances

  • CXCL16 protein, human
  • Chemokine CXCL16
  • Chemokines, CXC
  • Inflammation Mediators
  • Interleukin-8
  • Receptors, Scavenger