Mantelli Flavio, Schaffer Lana, Dana Reza, Head Steven R, Argüeso Pablo
Department of Ophthalmology, Schepens Eye Research Institute, Harvard Medical School, Boston, Massachusetts 02114, USA.
Invest Ophthalmol Vis Sci. 2009 Jun;50(6):2666-72. doi: 10.1167/iovs.08-2734. Epub 2008 Nov 14.
Glycoconjugates regulate a variety of biological events in mucosal surfaces, such as differentiation of postmitotic epithelial cells and maintenance of the wet-surfaced phenotype. This study aimed to identify the repertoire of genes (glycogenes) involved in biosynthesis of glycoconjugates in conjunctiva of normal subjects and patients with dry eye.
RNA from conjunctival impression cytology samples was amplified and hybridized to a custom-designed glycogene microarray. Intensity data were converted to expression values and analyzed by ANOVA. Microarray data for selected Notch glycogenes were confirmed by quantitative real-time PCR. Notch receptors and ligands were immunolocalized on conjunctival biopsies by confocal microscopy.
By microarray, 424 glycogenes were identified in normal conjunctival epithelium; galectins, glycosyltransferases, mucins, Notch signaling molecules, and proteoglycans were among the most highly expressed. In dry eye, 46 glycogenes were significantly downregulated, including five members of the Notch signaling pathway (Notch1, Notch 2, Notch 3, Jagged1, Delta1), four Wnt signaling molecules (Wnt4, -5A, Frizzled6, -7), and three heparan sulfate glycotransferases (HS2ST1, HS3ST6, EXTL2). Only interferon-induced transmembrane protein 1 was upregulated. By real-time PCR, expression ratios of Notch1, Notch 3, and Jagged1 in dry eye were 0.43, 0.56, and 0.50, respectively, compared to controls (P < 0.05). Notch1, Notch3, and Jagged1 were immunolocalized throughout the conjunctival epithelium, whereas Notch2 and Delta1 were distributed apically.
This study revealed the differential glycogene expression profiles in normal subjects and patients with dry eye. Downregulation of Notch signaling in dry eye may result in abnormal differentiation of the conjunctival epithelium and have implications in the pathogenesis of the disease.
糖缀合物调节黏膜表面的多种生物学事件,如终末分化上皮细胞的分化以及湿表面表型的维持。本研究旨在鉴定正常受试者和干眼患者结膜中参与糖缀合物生物合成的基因(糖基因)库。
结膜印片细胞学样本的RNA被扩增并与定制设计的糖基因微阵列杂交。强度数据被转换为表达值并通过方差分析进行分析。选定的Notch糖基因的微阵列数据通过定量实时PCR得到确认。Notch受体和配体通过共聚焦显微镜在结膜活检组织上进行免疫定位。
通过微阵列分析,在正常结膜上皮中鉴定出424个糖基因;半乳糖凝集素、糖基转移酶、黏蛋白、Notch信号分子和蛋白聚糖是表达最高的基因之一。在干眼中,46个糖基因显著下调,包括Notch信号通路的五个成员(Notch1、Notch 2、Notch 3、Jagged1、Delta1)、四个Wnt信号分子(Wnt4、-5A、Frizzled6、-7)和三个硫酸乙酰肝素糖基转移酶(HS2ST1、HS3ST6、EXTL2)。只有干扰素诱导的跨膜蛋白1上调。通过实时PCR,与对照组相比,干眼中Notch1、Notch 3和Jagged1的表达率分别为0.43、0.56和0.50(P < 0.05)。Notch1、Notch3和Jagged1在整个结膜上皮中免疫定位,而Notch2和Delta1分布在顶端。
本研究揭示了正常受试者和干眼患者中糖基因的差异表达谱。干眼中Notch信号的下调可能导致结膜上皮异常分化,并对该疾病的发病机制产生影响。