Delayed neutrophil apoptosis in chronic periodontitis patients

被引:63
作者
Gamonal, J
Sanz, M
O'Connor, A
Acevedo, A
Suarez, I
Sanz, A
Martínez, B
Silva, A
机构
[1] CSIC, Ctr Invest Biol, Dept Inmunol, E-28006 Madrid, Spain
[2] Univ Chile, Fac Odontol, Area Periodoncia, Dept Odontol Conservadora, Santiago, Chile
[3] Univ Complutense Madrid, Fac Odontol, Madrid, Spain
[4] Hosp Univ Princesa, Madrid, Spain
关键词
apoptosis; periodontitis; neutrophil; bax; GM-CSF; COLONY-STIMULATING FACTOR; PROGRAMMED CELL-DEATH; NECROSIS-FACTOR-ALPHA; EOSINOPHIL APOPTOSIS; DIFFERENTIAL EXPRESSION; IN-VITRO; ACTIVATION; BCL-2; BAX; TISSUE;
D O I
10.1034/j.1600-051X.2003.00350.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background, aims: Neutrophil cells constitute the first defense barrier against the oral bacterial challenge in the periodontium. Reduction of neutrophils could impair this response against periopathogenic bacteria such as Porphyromonas gingivalis . Our previous work implicates the apoptosis of neutrophils in the pathogenesis of periodontitis. We now demonstrate that granulocyte monocyte-colony stimulating factor (GM-CSF) present in the gingival crevicular fluid (GCF) and secreted during the immune response reduces the apoptosis of neutrophils. Methods: In this study, the presence of GM-CSF and tumor necrosis factor-alpha (TNF-alpha ) in GCF was determined in samples obtained from adult patients with periodontitis and from control subjects with clinically healthy gingiva. GCF was collected for 30 s using Periopaper(R) strips, and cytokines were quantified by ELISA. We used ex vivo culture of gingival tissue biopsies for 2 and 4 days in the presence of GM-CSF. Apoptosis was determined using the terminal TdT-mediated dUTP-biotin nick end labeling (TUNEL) technique, and expression of Bax by immunohistochemistry. Results: The presence of GM-CSF and TNF-alpha was detected in the majority of sites from periodontal patients (83.3% and 63.3%, respectively), presenting a total amount of 27.65 and 42.38 pg, respectively. GM-CSF reduces the neutrophil apoptosis determined by double staining with TUNEL and myeloperoxidase and by a reduction of Bax expression. Conclusions: These findings suggest a novel mechanism by which neutrophils specifically accumulate in adult patients with periodontitis.
引用
收藏
页码:616 / 623
页数:8
相关论文
共 54 条
[1]   Molecular control of neutrophil apoptosis [J].
Akgul, C ;
Moulding, DA ;
Edwards, SW .
FEBS LETTERS, 2001, 487 (03) :318-322
[2]  
[Anonymous], 1999, J PERIODONTOL, V70, P457
[3]  
BRACH MA, 1992, BLOOD, V80, P2920
[4]  
COHEN JJ, 1991, ADV IMMUNOL, V50, P55
[5]  
COHEN JJ, 1993, IMMUNOL TODAY, V14, P126, DOI 10.1016/0167-5699(93)90214-6
[6]  
COLOTTA F, 1992, BLOOD, V80, P2012
[7]   BRONCHIAL EPITHELIAL CELL-DERIVED CYTOKINES (G-CSF AND GM-CSF) PROMOTE THE SURVIVAL OF PERIPHERAL-BLOOD NEUTROPHILS INVITRO [J].
COX, G ;
GAULDIE, J ;
JORDANA, M .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 7 (05) :507-513
[8]   Cytokine-activated endothelial cells delay neutrophil apoptosis in vitro and in vivo: a role for granulocyte/macrophage colony-stimulating factor [J].
Coxon, A ;
Tang, T ;
Mayadas, TN .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (07) :923-933
[9]   Alterations in phagocyte function and periodontal infection [J].
Daniel, MA ;
VanDyke, TE .
JOURNAL OF PERIODONTOLOGY, 1996, 67 (10) :1070-1075
[10]   Cytokine-mediated Bax deficiency and consequent delayed neutrophil apoptosis: A general mechanism to accumulate effector cells in inflammation [J].
Dibbert, B ;
Weber, M ;
Nikolaizik, WH ;
Vogt, P ;
Schöni, MH ;
Blaser, K ;
Simon, HU .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (23) :13330-13335