Porphyromonas gingivalis gingipains cause defective macrophage migration towards apoptotic cells and inhibit phagocytosis of primary apoptotic neutrophils

被引:40
作者
Castro, Sowmya A. [1 ]
Collighan, Russell [1 ]
Lambert, Peter A. [1 ]
Dias, Irundika H. K. [1 ]
Chauhan, Parbata [1 ]
Bland, Charlotte E. [1 ]
Milic, Ivana [1 ]
Milward, Michael R. [2 ]
Cooper, Paul R. [2 ]
Devitt, Andrew [1 ]
机构
[1] Aston Univ, Aston Res Ctr Healthy Ageing, Sch Life & Hlth Sci, Birmingham B4 7ET, W Midlands, England
[2] Univ Birmingham, Sch Dent, Birmingham B5 7EG, W Midlands, England
基金
英国生物技术与生命科学研究理事会;
关键词
CYSTEINE PROTEINASES GINGIPAINS; PROTEASE-ACTIVATED RECEPTORS; PERIODONTAL-DISEASE; OUTER-MEMBRANE; IN-VITRO; CLEARANCE; CD14; RECOGNITION; CHEMOTAXIS; SURFACE;
D O I
10.1038/cddis.2016.481
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Periodontal disease is a prevalent chronic inflammatory condition characterised by an aberrant host response to a pathogenic plaque biofilm resulting in local tissue damage and frustrated healing that can result in tooth loss. Cysteine proteases (gingipains) from the key periodontal pathogen Porphyromonas gingivalis have been implicated in periodontal disease pathogenesis by inhibiting inflammation resolution and are linked with systemic chronic inflammatory conditions such as rheumatoid arthritis. Efficient clearance of apoptotic cells is essential for the resolution of inflammation and tissue restoration. Here we sought to characterise the innate immune clearance of apoptotic cells and its modulation by gingipains. We examined the capacity of gingipain-treated macrophages to migrate towards and phagocytose apoptotic cells. Lysine gingipain treatment of macrophages impaired macrophage migration towards apoptotic neutrophils. Furthermore, lysine gingipain treatment reduced surface expression levels of CD14, a key macrophage receptor for apoptotic cells, which resulted in reduced macrophage interactions with apoptotic cells. Additionally, while apoptotic cells and their derived secretome were shown to inhibit TNF-alpha- induced expression by P. gingivalis lipopolysaccharide, we demonstrated that gingipain preparations induced a rapid inflammatory response in macrophages that was resistant to the anti-inflammatory effects of apoptotic cells or their secretome. Taken together, these data indicate that P. gingivalis may promote the chronic inflammation seen in periodontal disease patients by multiple mechanisms, including rapid, potent gingipain-mediated inflammation, coupled with receptor cleavage leading to defective clearance of apoptotic cells and reduced anti-inflammatory responses. Thus, gingipains represent a potential therapeutic target for intervention in the management of chronic periodontal disease.
引用
收藏
页码:e2644 / e2644
页数:9
相关论文
共 58 条
[41]   Comparative properties of two cysteine proteinases (gingipains R), the products of two related but individual genes of Porphyromonas gingivalis [J].
Potempa, J ;
Mikolajczyk-Pawlinska, J ;
Brassell, D ;
Nelson, D ;
Thogersen, IB ;
Enghild, JJ ;
Travis, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (34) :21648-21657
[42]   THE MULTIPLE FORMS OF TRYPSIN-LIKE ACTIVITY PRESENT IN VARIOUS STRAINS OF PORPHYROMONAS-GINGIVALIS ARE DUE TO THE PRESENCE OF EITHER ARG-GINGIPAIN OR LYS-GINGIPAIN [J].
POTEMPA, J ;
PIKE, R ;
TRAVIS, J .
INFECTION AND IMMUNITY, 1995, 63 (04) :1176-1182
[43]   Surface molecule loss and bleb formation by human germinal center B cells undergoing apoptosis:: Role of apoptotic blebs in monocyte chemotaxis [J].
Segundo, C ;
Medina, F ;
Rodríguez, C ;
Martínez-Palencia, R ;
Leyva-Cobián, F ;
Brieva, JA .
BLOOD, 1999, 94 (03) :1012-1020
[44]   Resolution of inflammation: The beginning programs the end [J].
Serhan, CN ;
Savill, J .
NATURE IMMUNOLOGY, 2005, 6 (12) :1191-1197
[45]  
Sheets SM, 2008, FRONT BIOSCI-LANDMRK, V13, P3215
[46]   In-gel digestion for mass spectrometric characterization of proteins and proteomes [J].
Shevchenko, Andrej ;
Tomas, Henrik ;
Havlis, Jan ;
Olsen, Jesper V. ;
Mann, Matthias .
NATURE PROTOCOLS, 2006, 1 (06) :2856-2860
[47]   Microbial complexes in subgingival plaque [J].
Socransky, SS ;
Haffajee, AD ;
Cugini, MA ;
Smith, C ;
Kent, RL .
JOURNAL OF CLINICAL PERIODONTOLOGY, 1998, 25 (02) :134-144
[48]   Proteolysis of human monocyte CD14 by cysteine proteinases (Gingipains) from Porphyromonas gingivalis leading to lipopolysaccharide hyporesponsiveness [J].
Sugawara, S ;
Nemoto, E ;
Tada, H ;
Miyake, K ;
Imamura, T ;
Takada, H .
JOURNAL OF IMMUNOLOGY, 2000, 165 (01) :411-418
[49]   Proteolysis of CD14 on human gingival fibroblasts by arginine-specific cysteine proteinases from Porphyromonas gingivalis leading to down-regulation of lipopolysaccharide-induced interleukin-8 production [J].
Tada, H ;
Sugawara, S ;
Nemoto, E ;
Takahashi, N ;
Imamura, T ;
Potempa, J ;
Travis, J ;
Shimauchi, H ;
Takada, H .
INFECTION AND IMMUNITY, 2002, 70 (06) :3304-3307
[50]   Cleavage of Host Cytokeratin-6 by Lysine-Specific Gingipain Induces Gingival Inflammation in Periodontitis Patients [J].
Tancharoen, Salunya ;
Matsuyama, Takashi ;
Kawahara, Ko-Ichi ;
Tanaka, Kenji ;
Lee, Lyang-Ja ;
Machigashira, Miho ;
Noguchi, Kazuyuki ;
Ito, Takashi ;
Imamura, Takahisa ;
Potempa, Jan ;
Kikuchi, Kiyoshi ;
Maruyama, Ikuro .
PLOS ONE, 2015, 10 (02)