Miyazaki A, Kobayashi T, Suzuki T, Yoshie H, Hara K
Department of Periodontology, Niigata University School of Dentistry, Japan.
J Periodontal Res. 1997 Jul;32(5):439-46. doi: 10.1111/j.1600-0765.1997.tb00556.x.
Immunoglobulin G type II and III receptors (Fc gamma RII and Fc gamma RIII) are essential for polymorphonuclear leukocytic (PMNs) phagocytosis. Our previous study demonstrated a downregulation of Fc gamma RIII on PMNs in gingival crevicular fluid (GCF). To determine whether this receptor downregulation may contribute to the periodontal host defence borne by PMNs, we examined the correlation between Fc gamma RII and Fc gamma RIII expressions and the phagocytic capacity of GCF-PMNs. In order to verify at which level of cellular events the loss of Fc gamma R occurs, we quantified mRNA levels to assess a de novo synthesis of these receptors. GCF was collected from 21 patients with adult periodontitis by gingival crevicular washing. Autologous peripheral blood (PB) PMNs served as control. Surface expressions of Fc gamma Rs and phagocytic capacity via Fc gamma Rs were analysed by flow cytometry. The difference in Fc gamma R mRNA levels between GCF- and PB-PMNs was assessed by reverse transcription polymerase chain reaction (RT-PCR). The amplified products were visualized by agarose gel electrophoresis and the endproduct yields were quantified by computerized image-analysis. Both Fc gamma RII and Fc gamma RIII expressions and phagocytic capacity on GCF-PMNs were significantly lower than those on PB-PMNs (p < 0.001). The downregulation of Fc gamma Rs on GCF-PMNs significantly correlated with the phagocytic capacity (r = 0.66 for Fc gamma RIII, p < 0.01; r = 0.50 for Fc gamma RII, p < 0.05). The mRNA level of Fc gamma RIII of GCF-PMNs was significantly lower than that of PB-PMNs (p < 0.05). Thus, GCF-PMNs are characterized by the decreased surface expressions and mRNA levels of Fc gamma Rs, and the impaired phagocytosis.
免疫球蛋白G II型和III型受体(FcγRII和FcγRIII)对于多形核白细胞(PMN)的吞噬作用至关重要。我们之前的研究表明,龈沟液(GCF)中PMN上的FcγRIII表达下调。为了确定这种受体下调是否可能影响PMN介导的牙周宿主防御,我们研究了FcγRII和FcγRIII表达与GCF-PMN吞噬能力之间的相关性。为了验证FcγR缺失发生在细胞事件的哪个水平,我们对mRNA水平进行定量以评估这些受体的从头合成。通过龈沟冲洗从21例成人牙周炎患者中收集GCF。自体外周血(PB)PMN作为对照。通过流式细胞术分析FcγR的表面表达以及通过FcγR的吞噬能力。通过逆转录聚合酶链反应(RT-PCR)评估GCF-PMN和PB-PMN之间FcγR mRNA水平的差异。扩增产物通过琼脂糖凝胶电泳可视化,终产物产量通过计算机图像分析进行定量。GCF-PMN上的FcγRII和FcγRIII表达以及吞噬能力均显著低于PB-PMN(p < 0.001)。GCF-PMN上FcγR的下调与吞噬能力显著相关(FcγRIII的r = 0.66,p < 0.01;FcγRII的r = 0.50,p < 0.05)。GCF-PMN的FcγRIII mRNA水平显著低于PB-PMN(p < 0.05)。因此,GCF-PMN的特征在于FcγR的表面表达和mRNA水平降低以及吞噬作用受损。