Ida Hisashi, Boylan Sharon A, Weigel Andrea L, Hjelmeland Leonard M
Department of Biological Chemistry, University of California, Davis, California 95616-8794, USA.
Physiol Genomics. 2003 Nov 11;15(3):258-62. doi: 10.1152/physiolgenomics.00126.2003.
To evaluate the age-related changes in gene expression occurring in the complex of retinal pigmented epithelium, Bruch's membrane, and choroid (RPE/choroid), we examined the gene expression profiles of young adult (2 mo) and old (24 mo) male C57BL/6 mice. cDNA probe sets from individual animals were synthesized using total RNA isolated from the RPE/choroid of each animal. Probes were amplified using the Clontech SMART system, radioactively labeled, and hybridized to two different Clontech Atlas mouse cDNA arrays. From each age group, three independent triplicates were hybridized to the arrays. Statistical analyses were performed using the Significance Analysis of Microarrays program (SAM version 1.13; Stanford University). Selected array results were confirmed by semi-quantitative RT-PCR analysis. Of 2,340 genes represented on the arrays, approximately 60% were expressed in young and/or old mouse RPE/choroid. A moderate fraction (12%) of all expressed genes exhibited a statistically significant change in expression with age. Of these 150 genes, all but two, HMG14 and carboxypeptidase E, were upregulated with age. Many of these upregulated genes can be grouped into several broad functional categories: immune response, proteases and protease inhibitors, stress response, and neovascularization. RT-PCR results from six of six genes examined confirmed the differential change in expression with age of these genes. Our study provides likely candidate genes to further study their role in the development of age-related macular degeneration and other aging diseases affecting the RPE/choroid.
为了评估视网膜色素上皮、布鲁赫膜和脉络膜复合体(RPE/脉络膜)中发生的与年龄相关的基因表达变化,我们检测了年轻成年(2个月)和老年(24个月)雄性C57BL/6小鼠的基因表达谱。使用从每只动物的RPE/脉络膜中分离的总RNA合成来自个体动物的cDNA探针集。探针使用Clontech SMART系统进行扩增、放射性标记,并与两种不同的Clontech Atlas小鼠cDNA阵列杂交。从每个年龄组中,将三个独立的重复样本与阵列杂交。使用微阵列显著性分析程序(SAM版本1.13;斯坦福大学)进行统计分析。选定的阵列结果通过半定量RT-PCR分析进行确认。在阵列上代表的2340个基因中,约60%在年轻和/或老年小鼠的RPE/脉络膜中表达。所有表达基因中有一小部分(12%)表现出随年龄增长在表达上有统计学显著变化。在这150个基因中,除了HMG14和羧肽酶E这两个基因外,其他所有基因都随年龄上调。这些上调的基因中有许多可以归为几个广泛的功能类别:免疫反应、蛋白酶和蛋白酶抑制剂、应激反应和新生血管形成。所检测的六个基因的RT-PCR结果证实了这些基因随年龄表达的差异变化。我们的研究提供了可能的候选基因,以进一步研究它们在年龄相关性黄斑变性和其他影响RPE/脉络膜的衰老疾病发展中的作用。