Honma M, Hayakawa Y, Kosugi H, Koizumi F
Second Department of Pathology, Faculty of Medicine, Toyama Medical and Pharmaceutical University, Japan.
J Oral Pathol Med. 1998 Sep;27(8):399-404. doi: 10.1111/j.1600-0714.1998.tb01974.x.
The expression of mRNA encoding the inflammatory cytokines interleukin-1alpha (IL-1alpha), interleukin-1beta (IL-1beta), interleukin-6 (IL-6), interleukin-8 (IL-8) and tumor necrosis factor alpha(TNF-alpha) have been examined in radicular cysts by in situ hybridization. Furthermore, the biological activity of the contents of radicular cysts (RCC) has been assayed by adding extracts of RCC to cultured human gingival fibroblasts (HGFs) and analyzing the culture medium for the release of inflammatory cytokines. In the epithelial layer, keratinocytes expressed all cytokine mRNAs examined at various levels. Basal layer cells expressed mRNA for each cytokine. In the subepithelial granulation tissue of the cysts, fibroblasts and macrophages expressed mRNA for IL-6, IL-8, IL-1beta and TNF-alpha mRNA at varying levels; especially clear expression of TNF-alpha and IL-1beta mRNA was detected on macrophages. The infiltrating lymphoid cells, largely composed of T cells and plasma cells, expressed these cytokine mRNAs, especially those encoding IL-6 and IL-8, at various levels. In vitro analysis indicated dose-dependent release of both IL-6 and IL-8 by HGFs in response to RCC. After heating to 100 degrees C for 10 min, RCC almost completely failed to stimulate IL-6 release from HGFs. Furthermore, anti-IL-1beta antibody (neutralization test) did not prevent the stimulation of IL-6 release by RCC. Significant amounts of IL-6 and IL-8 were detected in RCC in two cases, and a trace amount of IL-1beta was detected in one case. This study demonstrated the wide expression of mRNA encoding inflammatory cytokines in radicular cyst tissues, and RCC itself was capable of stimulating IL-6 and IL-8 production from HGFs.
通过原位杂交技术检测了根端囊肿中编码炎性细胞因子白细胞介素-1α(IL-1α)、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、白细胞介素-8(IL-8)和肿瘤坏死因子α(TNF-α)的mRNA表达。此外,通过将根端囊肿内容物(RCC)提取物添加到培养的人牙龈成纤维细胞(HGFs)中,并分析培养基中炎性细胞因子的释放情况,检测了RCC的生物活性。在上皮层中,角质形成细胞以不同水平表达所有检测的细胞因子mRNA。基底层细胞表达每种细胞因子的mRNA。在囊肿的上皮下肉芽组织中,成纤维细胞和巨噬细胞以不同水平表达IL-6、IL-8、IL-1β和TNF-α的mRNA;尤其在巨噬细胞上检测到TNF-α和IL-1β mRNA的明显表达。浸润的淋巴细胞主要由T细胞和浆细胞组成,以不同水平表达这些细胞因子mRNA,尤其是编码IL-6和IL-8的mRNA。体外分析表明,HGFs对RCC的反应呈剂量依赖性释放IL-6和IL-8。加热至100℃ 10分钟后,RCC几乎完全不能刺激HGFs释放IL-6。此外,抗IL-1β抗体(中和试验)不能阻止RCC对IL-6释放的刺激。在两例RCC中检测到大量的IL-6和IL-8,在一例中检测到微量的IL-1β。本研究证明了根端囊肿组织中编码炎性细胞因子的mRNA广泛表达,且RCC本身能够刺激HGFs产生IL-6和IL-8。