Park Choul Yong, Zhuang Wenjuan, Lekhanont Kaevalin, Zhang Cheng, Cano Marisol, Lee Woo-Seok, Gehlbach Peter L, Chuck Roy S
Department of Ophthalmology, Johns Hopkins University, School of Medicine, Baltimore, MD, USA.
Mol Vis. 2007 Nov 29;13:2222-32.
To determine the effect of keratoconjunctivitis sicca, induced by botulinum toxin-B (BTX-B), on the inflammatory cytokine gene expression in the lacrimal gland (LG). And to determine the effect of various topical anti-inflammatory agents on the resulting cytokine levels.
Forty-two mice (eight-week-old, female, CBA/J) were divided into six groups. Four groups were injected with BTX-B into both lacrimal glands, one group was injected with saline into both LG (Sal, n=7), and one group served as an uninjected control (Con, n=7). The four groups of BTX-B injected mice were then assigned to a treatment group: 1. no additional treatment (BTX), 2. artificial tear treatment (AT), 3. Cyclosporine A (CSA) treatment, and 4. fluorometholone (FM) treatment (n=7 in each group). Corneal fluorescein staining was evaluated one, two, and four weeks after injection. LGs were harvested after two weeks (groups Con, Sal, and BTX) and four weeks (groups AT, CSA, and FM) after injection. Gene microarray analysis for inflammatory cytokines and their receptors, real time reverse-transcriptase polymerase chain reaction (RT-PCR), and immunofluorescent staining with anti-mouse CD3e monoclonal antibody were then performed on LG tissue.
BTX-B injection into the LG effectively induced dry eye in mice two and four weeks following injection. Microarray data identified the proinflammatory cytokines interleukin (IL)-1, tumor necrosis factor (TNF)-alpha, IL-12, and macrophage migration inhibitory factor (MIF) and the anti-inflammatory cytokines IL-10 and toll-interacting protein (Tollip) as candidates for validation by real time RT-PCR. MIF and IL-12 expression were elevated in BTX-B injected mice at weeks 2 and 4 regardless of treatment. Tollip and IL-1 expressions were increased in some groups after BTX-B injection regardless of the treatment type. Other cytokines showed no significant changes. LG structures were well maintained without significant T lymphocyte infiltration in all groups.
Ocular surface change induced by BTX-B injection resulted in an altered expression of various inflammatory cytokines in our murine dry eye model. Alteration of the pathology-induced cytokine profile by topical therapy is reported.
确定肉毒杆菌毒素B(BTX - B)诱导的干燥性角结膜炎对泪腺(LG)中炎性细胞因子基因表达的影响。并确定各种局部抗炎药对由此产生的细胞因子水平的影响。
将42只小鼠(8周龄,雌性,CBA/J)分为6组。4组双侧泪腺注射BTX - B,1组双侧泪腺注射生理盐水(Sal,n = 7),1组作为未注射对照(Con,n = 7)。然后将注射BTX - B的4组小鼠分配到治疗组:1. 不进行额外治疗(BTX),2. 人工泪液治疗(AT),3. 环孢素A(CSA)治疗,4. 氟米龙(FM)治疗(每组n = 7)。注射后1、2和4周评估角膜荧光素染色。注射后2周(Con、Sal和BTX组)和4周(AT、CSA和FM组)采集泪腺。然后对泪腺组织进行炎性细胞因子及其受体的基因芯片分析、实时逆转录聚合酶链反应(RT - PCR)以及用抗小鼠CD3e单克隆抗体进行免疫荧光染色。
向泪腺注射BTX - B在注射后2周和4周有效地诱导了小鼠干眼。基因芯片数据确定促炎细胞因子白细胞介素(IL)-1、肿瘤坏死因子(TNF)-α、IL - 12和巨噬细胞迁移抑制因子(MIF)以及抗炎细胞因子IL - 10和Toll相互作用蛋白(Tollip)为通过实时RT - PCR验证的候选因子。无论治疗如何,MIF和IL - 12在注射BTX - B的小鼠中第2周和第4周表达均升高。无论治疗类型如何,Tollip和IL - 1在注射BTX - B后的一些组中表达增加。其他细胞因子无显著变化。所有组的泪腺结构保持良好,无明显T淋巴细胞浸润。
在我们的小鼠干眼模型中,BTX - B注射引起的眼表变化导致各种炎性细胞因子表达改变。报道了局部治疗对病理诱导的细胞因子谱的改变。