Miyahara Teruyoshi, Kikuchi Takanobu, Akimoto Masayuki, Kurokawa Toru, Shibuki Hiroto, Yoshimura Nagahisa
Department of Ophthalmology, Shinshu University School of Medicine, Matsumoto, Japan.
Invest Ophthalmol Vis Sci. 2003 Oct;44(10):4347-56. doi: 10.1167/iovs.02-1032.
To systematically explore changes in gene expression in the retina of monkeys with laser-induced glaucoma and to validate the microarray data on eyes with experimental glaucoma.
Glaucoma was induced in the right eye of four monkeys by repeated argon laser photocoagulation of the trabecular meshwork. The left eye served as the control. Retinas were isolated from glaucomatous and control eyes 30 days after photocoagulation. Gene expression changes were analyzed by human microarray chips which displayed a total of 9182 elements including Expression Sequence Tag (EST) clones. Changes in the expression of some genes were further confirmed by real-time PCR analysis. Immunohistochemical studies to examine protein expression of some gene products were also done for several genes that showed up- or downregulation by the microarray analysis.
Two eyes with mild glaucoma and two with severe glaucoma were produced. In the mild and severe glaucomatous retina, the number of upregulated genes was 45 and 18, and the number of downregulated genes was 17 and 21, respectively. The number of genes that were up- or downregulated was 0.7% of all the genes examined. The real-time PCR analysis confirmed expression changes of some genes found in the microarray analysis. Ceruloplasmin was one of the upregulated genes, and it was found by immunohistochemical analyses to be expressed in Müller cells.
Gene expression profiles in laser-induced glaucomatous monkey retinas were determined, and only a very small population of genes was up- or downregulated in glaucomatous eyes. Upregulation of ceruloplasmin protein was found in the Müller cells.
系统探究激光诱导性青光眼猕猴视网膜中的基因表达变化,并验证实验性青光眼眼中的微阵列数据。
通过对小梁网进行反复氩激光光凝,诱导4只猕猴右眼患青光眼。左眼作为对照。光凝30天后,从青光眼和对照眼中分离视网膜。使用人微阵列芯片分析基因表达变化,该芯片共显示9182个元件,包括表达序列标签(EST)克隆。通过实时PCR分析进一步确认部分基因表达的变化。对于微阵列分析显示上调或下调的几个基因,还进行了免疫组织化学研究以检测一些基因产物的蛋白表达。
产生了2只轻度青光眼眼和2只重度青光眼眼。在轻度和重度青光眼视网膜中,上调基因的数量分别为45个和18个以及下调基因的数量分别为17个和21个。上调或下调的基因数量占所有检测基因的0.7%。实时PCR分析证实了微阵列分析中发现的部分基因的表达变化。铜蓝蛋白是上调基因之一,免疫组织化学分析发现其在Müller细胞中表达。
确定了激光诱导性青光眼猕猴视网膜的基因表达谱,青光眼眼中只有极少数基因上调或下调。在Müller细胞中发现了铜蓝蛋白的上调。