Zylberberg Claudia, Seamon Vanessa, Ponomareva Olga, Vellala Kavyasri, Deighan Molly, Azzarolo Ana Maria
Department of Biomedical Science, Florida Atlantic University, Charles E. Schmidt College of Science, Boca Raton, FL, USA.
Exp Eye Res. 2007 May;84(5):960-72. doi: 10.1016/j.exer.2007.02.002. Epub 2007 Feb 11.
Increased levels of the matrix metalloproteinases (MMPs)-2 and -9 have been found in tear fluids of patients with dry eye disease, suggesting that these MMPs may be implicated in the pathogenesis of this disease. One of the main causes of dry eye disease is lacrimal gland insufficiency. However, the contribution of the lacrimal gland (LG) to the expression and production of MMP-2 and MMP-9 in tears is not known. Since dry eye disease occurs more frequently in women, sex hormones, especially estrogens, have also been implicated in the pathogenesis of this disease. Estrogens have been shown to regulate the synthesis levels of MMP-2 and MMP-9 in several tissues, Thus, the purpose of these studies was to determine if: (1) rabbit lacrimal glands secrete MMP-2 and MMP-9; (2) MMP-2 and MMP-9 are produced by lacrimal epithelial cells and/or lacrimal lymphocytes; and (3) the expression, activity and level of these enzymes are regulated by sex hormones. Lacrimal epithelial cells (LEC) and lacrimal lymphocytes (LL) from sexually mature New Zealand White female rabbits were isolated, purified and cultured with and without 10(-6)M dihydrotestosterone (DHT) or 10(-6), 10(-8), 10(-9) and 10(-10)M 17beta-estradiol (E2). The culture supernatants were analyzed by zymography and western blotting (WB) using polyclonal anti-human MMP-2 and MMP-9 antibodies. LGs were also collected from rabbits 7 days after being sham-operated, ovariectomized (OVX), OVX treated with 4 mg/kg DHT, and OVX treated with 0.5 mg/kg of E2. LGs were collected and processed for RNA extraction as well as protein determination using WB and immunocytochemistry. The pro-forms of MMP-2 and MMP-9 were detected in primary LEC and LL culture medium by zymography and WB. Pro-MMP-2 and pro-MMP-9 were also detected at the gene and protein levels in the lacrimal glands of all four treatment groups, with the highest levels and gene expression found in the estrogen-treated group. These results suggest that both pro-MMP-2 and pro-MMP-9 are secreted by the lacrimal gland and appear to be up-regulated by estrogen. The role of the lacrimal MMPs in the pathogenesis of dry eye disease needs to be further investigated.
在干眼症患者的泪液中发现基质金属蛋白酶(MMPs)-2和-9水平升高,这表明这些MMPs可能与该疾病的发病机制有关。干眼症的主要原因之一是泪腺功能不全。然而,泪腺(LG)对泪液中MMP-2和MMP-9表达及产生的作用尚不清楚。由于干眼症在女性中更为常见,性激素,尤其是雌激素,也被认为与该疾病的发病机制有关。雌激素已被证明可调节多种组织中MMP-2和MMP-9的合成水平。因此,这些研究的目的是确定:(1)兔泪腺是否分泌MMP-2和MMP-9;(2)MMP-2和MMP-9是否由泪腺上皮细胞和/或泪腺淋巴细胞产生;以及(3)这些酶的表达、活性和水平是否受性激素调节。从性成熟的新西兰白兔雌性分离、纯化泪腺上皮细胞(LEC)和泪腺淋巴细胞(LL),并在添加和不添加10(-6)M双氢睾酮(DHT)或10(-6)、10(-8)、10(-9)和10(-10)M 17β-雌二醇(E2)的条件下进行培养。使用多克隆抗人MMP-2和MMP-9抗体通过酶谱法和蛋白质印迹法(WB)分析培养上清液。在假手术、卵巢切除(OVX)、用4mg/kg DHT处理的OVX以及用0.5mg/kg E2处理的OVX的兔7天后也收集泪腺。收集泪腺并进行处理以提取RNA以及使用WB和免疫细胞化学进行蛋白质测定。通过酶谱法和WB在原代LEC和LL培养基中检测到MMP-2和MMP-9的前体形式。在所有四个治疗组的泪腺中也在基因和蛋白质水平检测到前MMP-2和前MMP-9,在雌激素处理组中发现水平和基因表达最高。这些结果表明前MMP-2和前MMP-9均由泪腺分泌,并且似乎受雌激素上调。泪腺MMPs在干眼症发病机制中的作用需要进一步研究。