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小鼠氧诱导性视网膜病变中的综合基因表达谱

Comprehensive gene-expression profile in murine oxygen-induced retinopathy.

作者信息

Sato T, Kusaka S, Hashida N, Saishin Y, Fujikado T, Tano Y

机构信息

Department of Applied Visual Science, Osaka University Medical School, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

Br J Ophthalmol. 2009 Jan;93(1):96-103. doi: 10.1136/bjo.2008.142646. Epub 2008 Oct 6.

Abstract

BACKGROUND/AIMS: To investigate the correlation between the clinical course and gene-expression pattern in murine oxygen-induced retinopathy (OIR), a commonly used model of retinopathy of prematurity (ROP).

METHODS

OIR was induced in C57BL/6N mice by placing postnatal day 7 (P7) pups in 75% oxygen for 5 days. The clinical course of the OIR was evaluated on retinal flat-mounts after fluorescein isothiocyanate-conjugated dextran perfusion from P12 to P21. The expression values of 94 genes, selected by microarray analyses, were determined daily from P12 through P21 by RT-PCR with TaqMan low-density array (TLDA) and analysed by hierarchical clustering.

RESULTS

TLDA cluster analyses showed a homology of gene-expression pattern between P12 and P13 and between P16 and P17. Many genes associated with inflammation were upregulated on P12 and P13 when the degree of both central avascular area and central vasoconstriction were maximal, and the upregulation of the genes continued to P21. At P16 and P17 when extraretinal neovascularisation became most noticeable, several genes associated with angiogenesis, for example, vascular endothelial growth factor-A and angiopoietin-2, were most upregulated.

CONCLUSION

The gene-expression pattern was well correlated with the clinical appearance in murine OIR. These findings should contribute to the understanding of the pathological conditions in ROP.

摘要

背景/目的:在氧诱导性视网膜病变(OIR)小鼠模型中研究临床病程与基因表达模式之间的相关性,OIR是一种常用的早产儿视网膜病变(ROP)模型。

方法

将出生后第7天(P7)的C57BL/6N小鼠幼崽置于75%氧气环境中5天,诱导产生OIR。在从P12至P21进行异硫氰酸荧光素偶联葡聚糖灌注后,通过视网膜铺片评估OIR的临床病程。通过微阵列分析选择的94个基因的表达值,从P12至P21每天使用TaqMan低密度阵列(TLDA)通过逆转录聚合酶链反应(RT-PCR)进行测定,并通过层次聚类分析。

结果

TLDA聚类分析显示P12与P13之间以及P16与P17之间基因表达模式具有同源性。当中央无血管区和中央血管收缩程度最大时,许多与炎症相关的基因在P12和P13上调,并且这些基因的上调持续至P21。在视网膜外新生血管最明显的P16和P17,一些与血管生成相关的基因,例如血管内皮生长因子-A和血管生成素-2,上调最为明显。

结论

在小鼠OIR中,基因表达模式与临床表现密切相关。这些发现应有助于理解ROP的病理状况。

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