Garlet G P, Cardoso C R, Campanelli A P, Martins W, Silva J S
Department of Biological Sciences, School of Dentistry of Bauru, São Paulo University (FOB/USP), Bauru, São Paulo, Brazil.
J Periodontal Res. 2006 Dec;41(6):580-4. doi: 10.1111/j.1600-0765.2006.00908.x.
Inflammatory cytokines are thought to trigger periodontal tissue destruction. In addition to being regulated by anti-inflammatory mediators, their activity is under the control of suppressors of cytokine signaling (SOCS), which down-regulate the signal transduction as part of an inhibitory feedback loop. We therefore investigated the expression of SOCS-1, -2 and -3, and the cytokines tumor necrosis factor-alpha (TNF-alpha) and interleukin-10, in different forms of human periodontal diseases.
Quantitative polymerase chain reaction (RealTime-PCR) was performed with mRNA from gingival biopsies of control subjects and from that of patients with chronic gingivitis and chronic periodontitis.
Our results show that patients with chronic gingivitis and chronic periodontitis exhibit significantly higher SOCS-1, -2 and -3, TNF-alpha and interleukin-10 mRNA expression when compared with healthy controls. The data also demonstrate that SOCS-1 and -3 mRNA expression was higher in tissue from patients with chronic gingivitis than chronic periodontitis, while the levels of SOCS-2, TNF-alpha and interleukin-10 mRNA were similar in these groups.
The increased expression of SOCS-1, -2 and -3 mRNA in diseased periodontal tissues is believed to be involved in the down-regulation of inflammatory cytokine and Toll-like receptor signaling, and therefore in the attenuation of both the inflammatory reaction and disease severity. Furthermore, it is possible that variation in the levels of SOCS mRNA expressed in different forms of periodontal diseases may determine the stable or progressive nature of the lesions.
炎性细胞因子被认为会引发牙周组织破坏。除了受抗炎介质调节外,它们的活性还受细胞因子信号转导抑制因子(SOCS)的控制,SOCS作为抑制性反馈环的一部分下调信号转导。因此,我们研究了SOCS-1、-2和-3以及细胞因子肿瘤坏死因子-α(TNF-α)和白细胞介素-10在不同形式人类牙周疾病中的表达。
对对照组、慢性牙龈炎患者和慢性牙周炎患者牙龈活检组织的mRNA进行定量聚合酶链反应(实时荧光定量PCR)。
我们的结果显示,与健康对照组相比,慢性牙龈炎和慢性牙周炎患者的SOCS-1、-2和-3、TNF-α和白细胞介素-10 mRNA表达显著更高。数据还表明,慢性牙龈炎患者组织中SOCS-1和-3 mRNA表达高于慢性牙周炎患者,而这些组中SOCS-2、TNF-α和白细胞介素-10 mRNA水平相似。
患病牙周组织中SOCS-1、-2和-3 mRNA表达增加被认为参与了炎性细胞因子和Toll样受体信号转导的下调,因此参与了炎症反应减弱和疾病严重程度降低。此外,不同形式牙周疾病中表达的SOCS mRNA水平的变化可能决定了病变的稳定或进展性质。