Ishibashi Kazuki, Tian Jane, Handa James T
Michael Panitch Macular Degeneration Laboratory, Wilmer Eye Institute, Johns Hopkins Medical Institutes, Baltimore, Maryland 21287, USA.
Invest Ophthalmol Vis Sci. 2004 Sep;45(9):3291-301. doi: 10.1167/iovs.04-0168.
To determine the expression profiles of morphologically normal human retinal pigment epithelial (RPE) cells that originate from the macula and periphery.
Morphologically normal RPE cells from 15 human globes from donors aged 52 to 82 years old were laser capture microdissected. Total RNA from 5000 cells was SMART amplified, [33]P-labeled, and hybridized to a cDNA array containing 4325 known genes. Expression profiles were analyzed by hierarchical cluster analysis, Prediction Analysis of Microarrays (PAM), and Significance Analysis for Microarrays (SAM). Differentially expressed genes were evaluated further by real time RT-PCR.
The overall expression profiles of RPE cells from the macula and periphery were similar. Unsupervised and supervised hierarchical cluster analysis showed that patient genotype was a stronger separating factor than topographical location. SAM analysis identified 11 genes that were underexpressed by macular RPE cells. The expression patterns of these 11 genes were confirmed by real time RT-PCR, with 5 genes reaching statistical significance.
Whereas the overall expression profiles were similar between cells from the macula and periphery, subtle differential expression of five genes could contribute to RPE phenotypic differences based on topographic location.
确定源自黄斑和周边区域的形态正常的人视网膜色素上皮(RPE)细胞的表达谱。
对来自15个年龄在52至82岁供体的人眼球中形态正常的RPE细胞进行激光捕获显微切割。从5000个细胞中提取的总RNA进行SMART扩增、[33]P标记,并与包含4325个已知基因的cDNA阵列杂交。通过层次聚类分析、微阵列预测分析(PAM)和微阵列显著性分析(SAM)对表达谱进行分析。通过实时RT-PCR进一步评估差异表达基因。
黄斑和周边区域的RPE细胞的整体表达谱相似。无监督和有监督的层次聚类分析表明,患者基因型是比地形位置更强的分离因素。SAM分析确定了11个在黄斑RPE细胞中表达不足的基因。通过实时RT-PCR证实了这11个基因的表达模式,其中5个基因具有统计学意义。
虽然黄斑和周边区域的细胞之间的整体表达谱相似,但五个基因的细微差异表达可能导致基于地形位置的RPE表型差异。