Stone Richard A, Khurana Tejvir S
Department of Ophthalmology, University of Pennsylvania School of Medicine, Scheie Eye Institute, Philadelphia, PA 19104-6075, USA.
Vision Res. 2010 Nov 23;50(23):2322-33. doi: 10.1016/j.visres.2010.03.021. Epub 2010 Apr 2.
To understand the complex regulatory pathways that underlie the development of refractive errors, expression profiling has evaluated gene expression in ocular tissues of well-characterized experimental models that alter postnatal eye growth and induce refractive errors. Derived from a variety of platforms (e.g. differential display, spotted microarrays or Affymetrix GeneChips), gene expression patterns are now being identified in species that include chicken, mouse and primate. Reconciling available results is hindered by varied experimental designs and analytical/statistical features. Continued application of these methods offers promise to provide the much-needed mechanistic framework to develop therapies to normalize refractive development in children.
为了理解屈光不正发生发展背后复杂的调控通路,表达谱分析已在特征明确的实验模型的眼组织中评估基因表达,这些模型可改变出生后眼的生长并诱发屈光不正。基因表达模式源自多种平台(如差异显示、点阵微阵列或Affymetrix基因芯片),目前已在包括鸡、小鼠和灵长类动物等物种中得到鉴定。不同的实验设计以及分析/统计特征阻碍了对现有结果的整合。持续应用这些方法有望提供急需的机制框架,以开发使儿童屈光发育正常化的治疗方法。