Expression of fractalkine (CX3CL1) and its receptor, CX3CR1, in periodontal diseased tissue

被引:31
作者
Hosokawa, Y [1 ]
Nakanishi, T [1 ]
Yamaguchi, D [1 ]
Nakae, H [1 ]
Matsuo, T [1 ]
机构
[1] Univ Tokushima, Sch Dent, Dept Conservat Dent, Tokushima 7708504, Japan
关键词
CX3CR1; fractalkine; periodontal disease;
D O I
10.1111/j.1365-2249.2005.02675.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The regulatory role of chemokines and chemokine receptors on specific leucocyte recruitment into periodontal diseased tissue is poorly characterized. We observed that leucocytes infiltrating inflamed gingival tissue expressed marked levels of CX3CR1. In periodontal diseased tissue, the expression of fractalkine and CX3CR1 mRNA was detected by reverse transcription-polymerase chain reaction (RT-PCR) and further, fractalkine was distributed mainly on endothelial cells, as shown by immunohistochemistry. Moreover, we can detect CX3CR1-expressing cells infiltrated in periodontal diseased tissue by immunohistochemical staining. Furthermore, fractalkine production by human umbilical vein endothelial cells (HUVEC) was up-regulated by pathogen-associated molecular patterns (PAMPs), including Porphyromonas gingivalis lipopolysaccharide (LPS). Thus, these findings suggested that CX3CR1 and the corresponding chemokine, fractalkine may have an important regulatory role on specific leucocyte migration into inflamed periodontal tissue.
引用
收藏
页码:506 / 512
页数:7
相关论文
共 25 条
[1]   A new class of membrane-bound chemokine with a CX(3)C motif [J].
Bazan, JF ;
Bacon, KB ;
Hardiman, G ;
Wang, W ;
Soo, K ;
Rossi, D ;
Greaves, DR ;
Zlotnik, A ;
Schall, TJ .
NATURE, 1997, 385 (6617) :640-644
[2]  
Blaschke S, 2003, J RHEUMATOL, V30, P1918
[3]   GRAM-NEGATIVE SPECIES ASSOCIATED WITH ACTIVE DESTRUCTIVE PERIODONTAL LESIONS [J].
DZINK, JL ;
TANNER, ACR ;
HAFFAJEE, AD ;
SOCRANSKY, SS .
JOURNAL OF CLINICAL PERIODONTOLOGY, 1985, 12 (08) :648-659
[4]   Fractalkine and CX3CR1 mediate a novel mechanism of leukocyte capture, firm adhesion, and activation under physiologic flow [J].
Fong, AM ;
Robinson, LA ;
Steeber, DA ;
Tedder, TF ;
Yoshie, O ;
Imai, T ;
Patel, DD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (08) :1413-1419
[5]  
Foussat A, 2000, EUR J IMMUNOL, V30, P87, DOI 10.1002/1521-4141(200001)30:1<87::AID-IMMU87>3.0.CO
[6]  
2-7
[7]   Fractalkine (CX3CL1) as an amplification circuit of polarized Th1 responses [J].
Fraticelli, P ;
Sironi, M ;
Bianchi, G ;
D'Ambrosio, D ;
Albanesi, C ;
Stoppacciaro, A ;
Chieppa, M ;
Allavena, P ;
Ruco, L ;
Girolomoni, G ;
Sinigaglia, F ;
Vecchi, A ;
Mantovani, A .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (09) :1173-1181
[8]  
Fujihashi K, 1996, CLIN EXP IMMUNOL, V103, P422
[9]   DISTRIBUTION OF NATURAL-KILLER-CELLS IN PERIODONTAL-DISEASES - AN IMMUNOHISTOCHEMICAL STUDY [J].
FUJITA, S ;
TAKAHASHI, H ;
OKABE, H ;
OZAKI, Y ;
HARA, Y ;
KATO, I .
JOURNAL OF PERIODONTOLOGY, 1992, 63 (08) :686-689
[10]   Patterns of chemokines and chemokine receptors expression in different forms of human periodontal disease [J].
Garlet, GP ;
Martins, W ;
Ferreira, BR ;
Milanezi, CM ;
Silva, JS .
JOURNAL OF PERIODONTAL RESEARCH, 2003, 38 (02) :210-217