Wakabayashi R C, Iha D K, Niu J J, Johnson P W
Department of Stomatology, School of Dentistry, University of California, San Francisco 94143-0650, USA.
J Periodontal Res. 1997 Feb;32(2):215-24. doi: 10.1111/j.1600-0765.1997.tb00527.x.
Since cytokines play a critical role in tissue regeneration, we have assayed cytokine production by cells from tissue adherent to regenerative membranes. Cells were recovered from Gore-tex membranes in guided tissue regeneration (GTR) procedures to regenerate that attachment apparatus around teeth and from Gore-tex augmentation membranes (GTAM) used for guided gone regeneration (GBR) procedures in edentulous ridge augmentation with or without implant placement. Cells were screened for mineralized nodule formation in vitro to mRNA analysis to demonstrate that they could form mineralized tissue. Production in interleukin-1 alpha (IL-1 alpha) interleukin-1 beta (IL-1 beta), interferon-gamma (IFN-gamma) and interleukin-4 (IL-4) was evaluated by reverse transcribed-polymerase chain reaction (RT-PCR) of mRNA from rescued regenerative cells, human gingival fibroblasts and periodontal ligament (PDL) cells. Both the gingival fibroblast and PDL cells isolates produced all 4 cytokines. However, the cell isolates from the regenerative membranes had various profiles of cytokine expression. Most GTR cell isolates were positive for all 4 cytokines. IL-1 beta was produced by all 6 GTR cell isolates but was not detected at the same number of cycles of RT-PCR amplification in any of the 6 GBR cell isolates. IL-1 beta transcripts were also not observed in cells derived from a direct biopsy of GBR tissue. Cells were recovered from unexposed GBR membranes did not produce detectable amounts of IFN-gamma, whereas cells recovered from exposed GBR and all GTR membranes produced IFN-gamma. These findings indicate that cells from regenerative tissues express different cytokines and that exposure to the tissue to the oral cavity during healing may modulate this expression.
由于细胞因子在组织再生中起关键作用,我们检测了附着于再生膜的组织来源细胞产生细胞因子的情况。在引导组织再生(GTR)程序中,从用于围绕牙齿再生附着装置的戈尔特斯膜中回收细胞,以及在有无种植体植入的无牙颌骨增量引导骨再生(GBR)程序中,从戈尔特斯增量膜(GTAM)中回收细胞。对细胞进行体外矿化结节形成筛选及mRNA分析,以证明它们能够形成矿化组织。通过对回收的再生细胞、人牙龈成纤维细胞和牙周韧带(PDL)细胞的mRNA进行逆转录聚合酶链反应(RT-PCR),评估白细胞介素-1α(IL-1α)、白细胞介素-1β(IL-1β)、干扰素-γ(IFN-γ)和白细胞介素-4(IL-4)的产生情况。牙龈成纤维细胞和PDL细胞分离株均产生所有4种细胞因子。然而,来自再生膜的细胞分离株具有不同的细胞因子表达谱。大多数GTR细胞分离株对所有4种细胞因子呈阳性。所有6个GTR细胞分离株均产生IL-1β,但在6个GBR细胞分离株中的任何一个中,在相同数量的RT-PCR扩增循环中均未检测到。在GBR组织直接活检获得的细胞中也未观察到IL-1β转录本。从未暴露的GBR膜中回收的细胞未产生可检测量的IFN-γ,而从暴露的GBR膜和所有GTR膜中回收的细胞产生IFN-γ。这些发现表明,来自再生组织的细胞表达不同的细胞因子,并且在愈合过程中组织暴露于口腔可能会调节这种表达。