Microbiology Division, National Center for Toxicological Research, 3900 NCTR Rd, Jefferson, AR 72079, USA.
J Biomed Sci. 2012 Jun 20;19(1):58. doi: 10.1186/1423-0127-19-58.
Vaginal epithelial cells have receptors, signal transduction mechanisms, and cytokine secretion capabilities to recruit host defenses against Candida albicans infections. This research evaluates how probiotic lactobacilli affect the defensive epithelial response.
This study used quantitative reverse transcription-polymerase chain reaction assay (qRT-PCR), flow cytometry, and a multiplex immunoassay to observe changes in the regulation of gene expression related to cytokine responses in the VK2 (E6/E7) vaginal epithelial cell line treated with 17β-estradiol, exposed to probiotic Lactobacillus rhamnosus GR-1® and Lactobacillus reuteri RC-14® and challenged with C. albicans. Data were statistically evaluated by repeated measures analysis of variance and paired t-tests where appropriate.
C. albicans induced mRNA expression of genes related to inflammatory cytokine responses associated with nuclear factor-kappa B (NF-κB) and mitogen-activated protein kinase (MAPK) signal transduction pathways. 17β-estradiol suppressed expression of interleukin-1α (IL-1α), IL-6, IL-8, and tumor necrosis factor alpha (TNFα) mRNA. Probiotic lactobacilli suppressed C. albicans-induced nuclear factor-kappa B inhibitor kinase kinase alpha (Iκκα), Toll-like receptor-2 (TLR2), TLR6, IL-8, and TNFα, also suggesting inhibition of NF-κB signaling. The lactobacilli induced expression of IL-1α, and IL-1β mRNA, which was not inhibited by curcumin, suggesting that they induce an alternate inflammatory signal transduction pathway to NF-κB, such as the mitogen activated protein kinase and activator protein-1 (MAPK/AP-1) signal transduction pathway. Curcumin inhibited IL-13 secretion, suggesting that expression of this cytokine is mainly regulated by NF-κB signaling in VK2 cells.
The results suggest that C. albicans infection induces pro-inflammatory responses in vaginal epithelial cells, and estrogen and lactobacilli suppress expression of NF-κB-related inflammatory genes. Probiotic lactobacilli may induce IL-1α and IL-1β expression by an alternate signal transduction pathway, such as MAPK/AP-1. Activation of alternate signaling mechanisms by lactobacilli to modify epithelial cell cytokine production may be a mechanism for probiotic modulation of morbidity in vulvovaginal candidiasis.
阴道上皮细胞具有受体、信号转导机制和细胞因子分泌能力,可招募宿主防御来对抗白色念珠菌感染。本研究评估了益生菌乳杆菌如何影响防御性上皮反应。
本研究使用定量逆转录聚合酶链反应(qRT-PCR)、流式细胞术和多重免疫分析观察用 17β-雌二醇处理的 VK2(E6/E7)阴道上皮细胞系中与细胞因子反应相关的基因表达调控的变化,该细胞系暴露于益生菌鼠李糖乳杆菌 GR-1®和罗伊氏乳杆菌 RC-14®并受到白色念珠菌的挑战。数据通过重复测量方差分析和适当的配对 t 检验进行统计学评估。
白色念珠菌诱导与核因子-κB(NF-κB)和丝裂原激活蛋白激酶(MAPK)信号转导途径相关的炎症细胞因子反应相关基因的 mRNA 表达。17β-雌二醇抑制白细胞介素-1α(IL-1α)、IL-6、IL-8 和肿瘤坏死因子α(TNFα)mRNA 的表达。益生菌乳杆菌抑制白色念珠菌诱导的核因子-κB 抑制剂激酶激酶α(Iκκα)、Toll 样受体-2(TLR2)、TLR6、IL-8 和 TNFα,这也表明抑制 NF-κB 信号。乳杆菌诱导 IL-1α 和 IL-1β mRNA 的表达,姜黄素不能抑制其表达,这表明它们诱导与 NF-κB 不同的炎症信号转导途径,例如丝裂原激活蛋白激酶和激活蛋白-1(MAPK/AP-1)信号转导途径。姜黄素抑制 IL-13 的分泌,表明该细胞因子的表达主要受 VK2 细胞中 NF-κB 信号的调节。
结果表明,白色念珠菌感染诱导阴道上皮细胞产生促炎反应,雌激素和益生菌乳杆菌抑制 NF-κB 相关炎症基因的表达。益生菌乳杆菌可能通过 MAPK/AP-1 等替代信号转导途径诱导 IL-1α 和 IL-1β 的表达。乳杆菌通过激活替代信号机制来改变上皮细胞细胞因子的产生可能是益生菌调节外阴阴道念珠菌病发病机制的一种机制。