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本文引用的文献

1
Proinflammatory role of fractalkine (CX3CL1) in rheumatoid arthritis.趋化因子(CX3CL1)在类风湿性关节炎中的促炎作用。
J Rheumatol. 2003 Sep;30(9):1918-27.
2
G protein-coupled receptors in natural killer cells.自然杀伤细胞中的G蛋白偶联受体
J Leukoc Biol. 2003 Jul;74(1):16-24. doi: 10.1189/jlb.0103019.
3
Patterns of chemokines and chemokine receptors expression in different forms of human periodontal disease.人类不同形式牙周病中趋化因子及趋化因子受体的表达模式
J Periodontal Res. 2003 Apr;38(2):210-7. doi: 10.1034/j.1600-0765.2003.02012.x.
4
The presence of chemokine (MCP-1, MIP-1alpha, MIP-1beta, IP-10, RANTES)-positive cells and chemokine receptor (CCR5, CXCR3)-positive cells in inflamed human gingival tissues.在炎症状态下的人类牙龈组织中趋化因子(单核细胞趋化蛋白-1、巨噬细胞炎性蛋白-1α、巨噬细胞炎性蛋白-1β、干扰素诱导蛋白-10、调节激活正常T细胞表达和分泌因子)阳性细胞和趋化因子受体(CC趋化因子受体5、CXC趋化因子受体3)阳性细胞的存在情况。
Cytokine. 2002 Oct 21;20(2):70-7. doi: 10.1006/cyto.2002.1985.
5
Macrophage inflammatory protein 3alpha-CC chemokine receptor 6 interactions play an important role in CD4+ T-cell accumulation in periodontal diseased tissue.巨噬细胞炎性蛋白3α-CC趋化因子受体6的相互作用在牙周病组织中CD4 + T细胞的积聚中起重要作用。
Clin Exp Immunol. 2002 Jun;128(3):548-54. doi: 10.1046/j.1365-2249.2002.01865.x.
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Chemokines in human periodontal disease tissues.人类牙周病组织中的趋化因子。
Clin Exp Immunol. 2001 Jul;125(1):134-41. doi: 10.1046/j.1365-2249.2001.01511.x.
7
Chemokines in immunity.免疫中的趋化因子。
Adv Immunol. 2001;78:57-110. doi: 10.1016/s0065-2776(01)78002-9.
8
Involvement of T-lymphocytes in periodontal disease and in direct and indirect induction of bone resorption.T淋巴细胞在牙周病以及骨吸收的直接和间接诱导中的作用。
Crit Rev Oral Biol Med. 2001;12(2):125-35. doi: 10.1177/10454411010120020301.
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Fractalkine (CX3CL1) as an amplification circuit of polarized Th1 responses.趋化因子(CX3CL1)作为极化Th1反应的放大回路。
J Clin Invest. 2001 May;107(9):1173-81. doi: 10.1172/JCI11517.
10
Expression and regulation of chemokine receptors in human natural killer cells.趋化因子受体在人自然杀伤细胞中的表达与调控
Blood. 2001 Jan 15;97(2):367-75. doi: 10.1182/blood.v97.2.367.

趋化因子(CX3CL1)及其受体CX3CR1在牙周病组织中的表达。

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

作者信息

Hosokawa Y, Nakanishi T, Yamaguchi D, Nakae H, Matsuo T

机构信息

Department of Conservative Dentistry, Tokushima University School of Dentistry, Tokushima, Japan.

出版信息

Clin Exp Immunol. 2005 Mar;139(3):506-12. doi: 10.1111/j.1365-2249.2005.02675.x.

DOI:10.1111/j.1365-2249.2005.02675.x
PMID:15730397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1809327/
Abstract

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.

摘要

趋化因子和趋化因子受体对特定白细胞募集到牙周病组织中的调节作用目前还不太清楚。我们观察到,浸润在发炎牙龈组织中的白细胞表达了高水平的CX3CR1。在牙周病组织中,通过逆转录聚合酶链反应(RT-PCR)检测到fractalkine和CX3CR1 mRNA的表达,此外,免疫组织化学显示,fractalkine主要分布在内皮细胞上。此外,通过免疫组织化学染色,我们可以检测到浸润在牙周病组织中的CX3CR1表达细胞。此外,人脐静脉内皮细胞(HUVEC)产生的fractalkine被包括牙龈卟啉单胞菌脂多糖(LPS)在内的病原体相关分子模式(PAMP)上调。因此,这些发现表明,CX3CR1和相应的趋化因子fractalkine可能对特定白细胞迁移到发炎的牙周组织中具有重要的调节作用。