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

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.

[1]  M. Farquhar,et al.  THE DEVELOPMENT OF NEUTROPHILIC POLYMORPHONUCLEAR LEUKOCYTES IN HUMAN BONE MARROW , 1971, The Journal of experimental medicine.

[2]  P. E. Van den Steen,et al.  Neutrophil gelatinase B potentiates interleukin-8 tenfold by aminoterminal processing, whereas it degrades CTAP-III, PF-4, and GRO-alpha and leaves RANTES and MCP-2 intact. , 2000, Blood.

[3]  L. Francetti,et al.  [Congenital neutrophil defects and periodontal diseases]. , 2000, Minerva stomatologica.

[4]  G. Garlet,et al.  Chemokines in Oral Inflammatory Diseases: Apical Periodontitis and Periodontal Disease , 2007, Journal of dental research.

[5]  G. Opdenakker,et al.  GCP-2/CXCL6 synergizes with other endothelial cell-derived chemokines in neutrophil mobilization and is associated with angiogenesis in gastrointestinal tumors. , 2005, Experimental cell research.

[6]  A. Kantarcı,et al.  Lipoxin signaling in neutrophils and their role in periodontal disease. , 2005, Prostaglandins, leukotrienes, and essential fatty acids.

[7]  D. Kreutzer,et al.  Localization of interleukin-8 in human gingival tissues. , 1995, Oral microbiology and immunology.

[8]  Paul Rutgeerts,et al.  CXCR1‐binding chemokines in inflammatory bowel diseases: down‐regulated IL‐8/CXCL8 production by leukocytes in Crohn's disease and selective GCP‐2/CXCL6 expression in inflamed intestinal tissue , 2004, European journal of immunology.

[9]  Ji Ming Wang,et al.  Granulocyte chemotactic protein‐2 and related CXC chemokines: from gene regulation to receptor usage , 1997, Journal of leukocyte biology.

[10]  C. Cao,et al.  Polymorphonuclear neutrophils and their mediators in gingival tissues from generalized aggressive periodontitis. , 2001, Journal of periodontology.

[11]  T. Kucharzik,et al.  Intestinal Microvascular Endothelium and Innate Immunity in Inflammatory Bowel Disease: a Second Line of Defense? , 2006, Infection and Immunity.

[12]  G. Opdenakker,et al.  Human and bovine granulocyte chemotactic protein-2: complete amino acid sequence and functional characterization as chemokines. , 1993, Biochemistry.

[13]  C. Rudack,et al.  The primary role in biologic activity of the neutrophil chemokines IL-8 and GRO-alpha in cultured nasal epithelial cells. , 2003, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

[14]  H. Birkedal‐Hansen Role of Matrix Metalloproteinases in Human Periodontal Diseases. , 1993, Journal of periodontology.

[15]  C. Rudack,et al.  Neutrophil chemokines in cultured nasal fibroblasts , 2002, Allergy.

[16]  S. Socransky,et al.  "Checkerboard" DNA-DNA hybridization. , 1994, BioTechniques.

[17]  Rafael A Irizarry,et al.  Exploration, normalization, and summaries of high density oligonucleotide array probe level data. , 2003, Biostatistics.

[18]  Ji Ming Wang,et al.  Differential usage of the CXC chemokine receptors 1 and 2 by interleukin-8, granulocyte chemotactic protein-2 and epithelial-cell-derived neutrophil attractant-78. , 1998, European journal of biochemistry.

[19]  N. Lang,et al.  Detection of interleukin-8 and matrix metalloproteinases transcripts in healthy and diseased gingival biopsies by RNA/PCR. , 1993, Journal of periodontal research.

[20]  Checkerboard assessments of serum antibodies to oral microbiota as surrogate markers of clinical periodontal status. , 2008, Journal of clinical periodontology.

[21]  A. Kantarcı,et al.  Neutrophil-mediated tissue injury in periodontal disease pathogenesis: findings from localized aggressive periodontitis. , 2003, Journal of periodontology.

[22]  Paul Pavlidis,et al.  Transcriptomes in Healthy and Diseased Gingival Tissues , 2008 .

[23]  S. Husson,et al.  Gelatinase B/MMP-9 and neutrophil collagenase/MMP-8 process the chemokines human GCP-2/CXCL6, ENA-78/CXCL5 and mouse GCP-2/LIX and modulate their physiological activities. , 2003, European journal of biochemistry.

[24]  D. Aeppli,et al.  Interleukin-1 alpha, interleukin-8 and interferon-alpha levels in gingival crevicular fluid. , 1996, Journal of periodontal research.

[25]  R. Page,et al.  The host response to the microbial challenge in periodontitis: assembling the players. , 1997, Periodontology 2000.

[26]  N. Lang,et al.  Neutrophil migration into the gingival sulcus is associated with transepithelial gradients of interleukin-8 and ICAM-1. , 1998, Journal of periodontology.