Papadopoulou Margarita, Papadaki Helen, Zolota Vasiliki, Gartaganis Sotirios P
a Department of Ophthalmology, School of Medicine , University of Patras , Rion , Greece.
b Department of Ophthalmology , University Hospital of Coventry and Warwickshire , UK.
Curr Eye Res. 2017 Jun;42(6):880-889. doi: 10.1080/02713683.2016.1257726. Epub 2017 Jan 13.
To (i) determine expression patterns of lysyl oxidase-like 1 (LOXL1), fibrillin-1 (FBN1), transforming growth factor beta-1 (TGF-β1), and cyclooxygenase-2 (COX-2) in lens epithelium and anterior lens capsule in pseudoexfoliation (PEX) syndrome and (ii) delineate the roles of these proteins in the etiopathogenesis of PEX.
Study participants, all of whom had undergone cataract surgery, comprised 47 patients with and 27 patients without (controls) PEX syndrome. Immunohistochemistry on paraffin sections of lens capsule and lens epithelium was performed.
Immunoexpression of LOXL1 and FBN1 on the outer surface of the lens capsule was significantly higher (p < 0.001), and nuclear immunopositivity for LOXL1 was more frequently observed (p = 0.017), in PEX patients compared with control patients. Cytoplasmic expression of LOXL1 and COX-2 was significantly lower (p = 0.015 and p = 0.042, respectively) in PEX patients compared with controls. TGF-β1 exhibited diffuse immunostaining detected in all cell layers in PEX patients (p <0.001). Significant direct correlations of cytoplasmic LOXL1 with FBN1 and TGF-β1, and of COX-2 with FBN1, TGF-β1, and LOXL-1, were observed only in PEX patients.
Results of our study provide valuable information vis-à-vis expression and localization of TGF-β1, LOXL1, and FBN1, as well as their associations in the lens epithelium and lens capsule. These data not only advance our knowledge of the etiopathogenesis of PEX syndrome, but also include novel findings, for example, immunostaining patterns of TGF-β1 in PEX syndrome. We suggest that COX-2 plays a role in the pathobiology of PEX syndrome and should be the subject of future investigations.
(i) 确定赖氨酰氧化酶样1(LOXL1)、原纤维蛋白-1(FBN1)、转化生长因子β-1(TGF-β1)和环氧化酶-2(COX-2)在假性剥脱(PEX)综合征患者晶状体上皮和晶状体前囊膜中的表达模式;(ii) 阐明这些蛋白在PEX发病机制中的作用。
研究参与者均为接受过白内障手术的患者,其中47例患有PEX综合征,27例未患(对照组)。对晶状体囊膜和晶状体上皮的石蜡切片进行免疫组织化学检测。
与对照组患者相比,PEX患者晶状体囊膜外表面的LOXL1和FBN1免疫表达显著更高(p < 0.001),且更频繁观察到LOXL1的核免疫阳性(p = 0.017)。与对照组相比,PEX患者中LOXL1和COX-2的细胞质表达显著更低(分别为p = 0.015和p = 0.042)。在PEX患者的所有细胞层中均检测到TGF-β1呈弥漫性免疫染色(p <0.001)。仅在PEX患者中观察到细胞质LOXL1与FBN1和TGF-β1、COX-2与FBN1、TGF-β1和LOXL-1之间存在显著的直接相关性。
我们的研究结果提供了关于TGF-β1、LOXL1和FBN1的表达、定位及其在晶状体上皮和晶状体囊膜中的关联的有价值信息。这些数据不仅增进了我们对PEX综合征发病机制的了解,还包括新的发现,例如PEX综合征中TGF-β1的免疫染色模式。我们认为COX-2在PEX综合征的病理生物学中起作用,应成为未来研究的主题。