Zhang Xiao-Hui, Feng Zhao-Hui, Zhang Yi
Department of Ophthalmology, the Second Affiliated Hospital of Xi'an Jiaotong University Medical College, Xi'an 710004, Shaanxi Province, China.
Int J Ophthalmol. 2014 Dec 18;7(6):941-6. doi: 10.3980/j.issn.2222-3959.2014.06.05. eCollection 2014.
To investigate if pigment epithelium-derived factor (PEDF) has any protective effect on the retinal Müller cells of Sprague-Dawley rats suffering from diabetes mellitus.
Sixty Sprague-Dawley rats were randomly divided into a negative control group, a group receiving 0.1 µg/µL PEDF, another group receiving 0.2 µg/µL PEDF, and a group receiving balanced salt solution (BSS). Rats in both the PEDF and BSS groups were treated intravitreally based on previously established diabetic models. After 4wk of treatment, morphological alterations of Müller cells and protein expression of glutamine synthase (GS) and glial fibrillary acidic protein (GFAP) were analyzed.
PEDF at either 0.1 µg/µL or 0.2 µg/µL significantly improved the structures of both nuclei and organelles of Müller cells compared to the BSS-treated group. Expression of GS was significantly higher in the 0.2 µg/µL PEDF group than that in the BSS group (P=0.012), but expression of GFAP was significantly lower in the 0.2 µg/µL PEDF group than that in the BSS group (P=0.000); however, there were no significant differences in expression of these proteins between the 0.1 µg/µL PEDF group and the BSS group (P=0.608, P=0.152).
PEDF protects the morphological ultrastructure of Müller cells, improves the expression of glutamate synthase and prevents cell gliosis.
研究色素上皮衍生因子(PEDF)对糖尿病斯普拉格-道利大鼠视网膜Müller细胞是否具有保护作用。
将60只斯普拉格-道利大鼠随机分为阴性对照组、接受0.1μg/μL PEDF的组、接受0.2μg/μL PEDF的组和接受平衡盐溶液(BSS)的组。基于先前建立的糖尿病模型,对PEDF组和BSS组的大鼠进行玻璃体腔内注射治疗。治疗4周后,分析Müller细胞的形态学改变以及谷氨酰胺合成酶(GS)和胶质纤维酸性蛋白(GFAP)的蛋白表达。
与BSS治疗组相比,0.1μg/μL或0.2μg/μL的PEDF均显著改善了Müller细胞核和细胞器的结构。0.2μg/μL PEDF组中GS的表达显著高于BSS组(P = 0.012),但0.2μg/μL PEDF组中GFAP的表达显著低于BSS组(P = 0.000);然而,0.1μg/μL PEDF组和BSS组之间这些蛋白的表达没有显著差异(P = 0.608,P = 0.152)。
PEDF可保护Müller细胞的形态超微结构,改善谷氨酸合成酶的表达并防止细胞胶质增生。