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[血管内皮生长因子和缺氧对视网膜色素上皮细胞中视蛋白分泌的影响]

[The effect of vascular endothelial growth factor and hypoxia on the secretion of opticin in retinal pigment epithelium cells].

作者信息

Ma Jin, Zhu Tie-pei, Zhang Qian-ru, Ou Hui-lin

机构信息

Eye Center of Second Affiliated Hospital, Medical College of Zhejiang University, Hangzhou 310009, China.

出版信息

Zhonghua Yan Ke Za Zhi. 2011 Nov;47(11):1012-8.

Abstract

OBJECTIVE

To evaluate the role of vascular endothelial growth factor or hypoxia on the secretion of opticin in retinal pigment epithelium cells.

METHODS

Human RPE cells were cultured, the third to sixth passage of retinal pigment epithelium (RPE) cells were placed in 6-well culture plates at a density of 4 × 10(4)/well. For hypoxia experiment, the cells were cultured under hypoxic condition for different times. For vascular endothelial growth factor (VEGF) experiment, the media was changed to DMEM containing different concentration VEGF (1, 10, 50, 100 µg/L) for 24 h respectively. VEGF mRNA levels were determined by RT-RCR method. The protein content of opticin in RPE cells or culture media was detected by Western blot. Matrix metalloproteinase activity in culture media was analysis by zymography. One way ANOVA was used to test the comparisons between experimental groups and control group.

RESULTS

Western blot experiment showed the opticin expression was not changed in RPE cells after hypoxia treatment, however was significantly decreased in culture media. Compared with control group (0.21 ± 0.03). The relative density of VEGF mRNA levels (0.81 ± 0.04, 0.67 ± 0.07) in RPE cells were increased after 12 h or 24 h hypoxia treatment (F = 483.60, P < 0.05). Opticin expression in RPE cells was also remain unchanged after vary concentration VEGF addition treatment (F = 2.16, P > 0.05), the relative density of opticin expression in VEGF conditioned culture medium were 0.65 ± 0.02, 0.52 ± 0.04, 0.23 ± 0.03, 0.30 ± 0.03 respectively, and the difference in culture media was significant compared to control group (0.73 ± 0.04) (F = 141.38, P < 0.05). Zymography indicate a matrix metalloproteinases type 2 digest band, the activities were enhanced with VEGF increasing. The decrease of opticin in culture media after VEGF treatment could be inhibited by low condition of EDTA.

CONCLUSION

VEGF and hypoxia have an effect on the on the secretion of opiticin in RPE cells, it may be contributed to the increasing levels of matrix metalloproteinases type 2.

摘要

目的

评估血管内皮生长因子或缺氧对视网膜色素上皮细胞中视锥蛋白分泌的作用。

方法

培养人视网膜色素上皮(RPE)细胞,将第三代至第六代RPE细胞以4×10⁴/孔的密度接种于6孔培养板中。对于缺氧实验,将细胞在缺氧条件下培养不同时间。对于血管内皮生长因子(VEGF)实验,分别将培养基更换为含有不同浓度VEGF(1、10、50、100μg/L)的DMEM培养24小时。通过RT-RCR法测定VEGF mRNA水平。用蛋白质免疫印迹法检测RPE细胞或培养基中视锥蛋白的蛋白质含量。通过酶谱分析法分析培养基中的基质金属蛋白酶活性。采用单因素方差分析来检验实验组与对照组之间的差异。

结果

蛋白质免疫印迹实验显示,缺氧处理后RPE细胞中视锥蛋白表达未改变,但培养基中视锥蛋白表达显著降低。与对照组(0.21±0.03)相比,缺氧处理12小时或24小时后RPE细胞中VEGF mRNA水平的相对密度(0.81±0.04,0.67±0.07)升高(F=483.60,P<0.05)。添加不同浓度VEGF处理后RPE细胞中视锥蛋白表达也保持不变(F=2.16,P>0.05),VEGF条件培养基中视锥蛋白表达的相对密度分别为0.65±0.02、0.52±0.04、0.23±0.03、0.30±0.03,与对照组(0.73±0.04)相比,培养基中的差异具有显著性(F=141.38,P<0.05)。酶谱分析显示有一条2型基质金属蛋白酶消化带,其活性随VEGF增加而增强。低浓度EDTA可抑制VEGF处理后培养基中视锥蛋白的减少。

结论

VEGF和缺氧对RPE细胞中视锥蛋白的分泌有影响,这可能与2型基质金属蛋白酶水平升高有关。

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