首页> 外文期刊>Cornea >Interleukin-1 receptor-1-deficient mice show attenuated production of ocular surface inflammatory cytokines in experimental dry eye.
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Interleukin-1 receptor-1-deficient mice show attenuated production of ocular surface inflammatory cytokines in experimental dry eye.

机译:IL-1受体-1缺陷型小鼠在实验性干眼症中显示出眼表炎性细胞因子的产生减少。

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PURPOSE: To compare inflammatory cytokine and defensin expression in response to experimental dry eye (EDE) in interleukin-1 receptor-1 (IL-1R1)-deficient (KO) mice with age-matched wild-type mice (WT). METHODS: EDE was induced by subcutaneous scopolamine injection, exposure to low humidity, and an air draft for 5 days in 4- to 6-week-old KO and WT mice. Expression of cytokines IL-1 alpha, IL-1 beta, tumor necrosis factor (TNF)-alpha, IL-6, and mouse beta-defensins (mBD)-1, mBD-2, and mBD-3 was evaluated by real-time polymerase chain reaction in scraped corneal epithelial cells and whole conjunctival tissues. A multiplex bead assay was performed to quantitate IL-1 alpha, IL-2, IL-4, IL-10, interferon (IFN)-gamma, and TNF-alpha levels in tear fluid, and an enzyme immunoassay was used to quantitate IL-1 beta levels in tear fluid. RESULTS: EDE significantly increased RNA transcripts for IL-1 alpha and beta in the conjunctiva and for TNF-alpha in the corneal epithelium of WT mice. Levels of IL-1 alpha, IL-1 beta, and IL-6 were significantly lower in the corneal epithelium and conjunctiva, and TNF-alpha was significantly lower in the cornea of KO mice after 5 days of EDE than WT mice. Tear fluid IL-1 alpha concentration increased above baseline on days 2-4 of EDE in WT and KO mice. A similar pattern was observed for tear TNF-alpha. Tear IL-1 beta increased throughout the 5 days of EDE in WT and KO mice. IFN-gamma, IL-2, IL-4, and IL-10 were undetectable in tear fluid of either strain before or after EDE. Corneal mBD-1 mRNA expression was unchanged and conjunctival mBD-1 transcripts decreased in WT and increased in KO mice with EDE. Untreated WT corneas, but not those of KO mice, expressed mBD-2 transcripts, whereas in the conjunctiva, mBD-2 increased in WT and decreased in KO mice with EDE. Corneal mBD-3 mRNA expression was undetected in WT mice, but increased after EDE in KO mice. Conjunctival mBD-3 transcripts were only detected in WT with EDE. CONCLUSIONS: These findings indicate that IL-1 signaling is responsible in part for the increased expression of inflammatory cytokines and the changes in mBDs by the ocular surface tissues in response to desiccating stress. These results show the important regulatory aspects of IL-1 on ocular surface epithelial inflammation.
机译:目的:比较白细胞介素1受体1(IL-1R1)缺陷(KO)小鼠和年龄匹配的野生型小鼠(WT)对实验性干眼症(EDE)的反应中炎症细胞因子和防御素的表达。方法:通过皮下注射东pol碱,暴露于低湿环境和通气5到4至6周龄的KO和WT小鼠,诱导EDE。细胞因子IL-1α,IL-1β,肿瘤坏死因子(TNF)-α,IL-6和小鼠β-防御素(mBD)-1,mBD-2和mBD-3的表达通过实时-角膜上皮细胞和整个结膜组织中的时间聚合酶链反应。进行多重珠试验以定量泪液中的IL-1α,IL-2,IL-4,IL-10,干扰素(IFN)-γ和TNF-α水平,并使用酶免疫法定量IL泪液中的-1β水平。结果:EDE显着增加了结膜炎小鼠结膜中IL-1α和β以及TNF-α的RNA转录本。 EDE 5天后,KO小鼠的角膜上皮和结膜中IL-1α,IL-1β和IL-6的水平显着低于WT小鼠,而TNF-α显着降低。 WT和KO小鼠在EDE的第2-4天,泪液IL-1α浓度增加至基线以上。对于泪液TNF-α观察到相似的模式。 WT和KO小鼠在EDE的整个5天中,泪液IL-1β均升高。在EDE之前或之后的任一菌株的泪液中均未检测到IFN-γ,IL-2,IL-4和IL-10。在具有EDE的WT中,角膜mBD-1 mRNA的表达没有变化,结膜mBD-1转录物在WT中降低,在KO小鼠中升高。未经治疗的野生型角膜,但不是KO小鼠的,表达mBD-2转录本,而在结膜中,mBD-2在WT中增加,而在有EDE的KO小鼠中降低。在WT小鼠中未检测到角膜mBD-3 mRNA表达,但在KO小鼠中在EDE后增加了角膜mBD-3 mRNA表达。结膜mBD-3转录物仅在具有EDE的WT中检测到。结论:这些发现表明,IL-1信号传导部分负责炎性细胞因子的表达增加以及眼表组织响应干燥压力而引起的mBDs变化。这些结果表明IL-1对眼表上皮发炎的重要调控方面。

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