首页> 外文期刊>Investigative ophthalmology & visual science >Downregulation of cone-specific gene expression and degeneration of cone photoreceptors in the Rpe65-/- mouse at early ages.
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Downregulation of cone-specific gene expression and degeneration of cone photoreceptors in the Rpe65-/- mouse at early ages.

机译:早期,Rpe65-/-小鼠中视锥细胞特异性基因表达的下调和视锥细胞感光细胞的变性。

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PURPOSE: RPE65 is essential for the generation of 11-cis retinal. Rod photoreceptors in the RPE65-knockout (Rpe65(-/-)) mouse are known to degenerate slowly with age. This study was designed to examine cone photoreceptors and the expression of cone-specific genes in the Rpe65(-/-) mouse. METHODS: Gene expression changes were identified by microarray and confirmed by real-time RT-PCR. Cone photoreceptors were stained by peanut agglutinin (PNA) lectin in the flatmounted retina. The 9- or 11-cis retinal was supplied by intraperitoneal injections. RESULTS: The short-wavelength (SWL) cone opsin mRNA was markedly decreased at 2 weeks of age, whereas the decrease in the middle-wavelength (MWL) cone opsin mRNA occurred relatively later in age. In contrast, the rhodopsin mRNA level did not show any significant change at all the ages analyzed. Consistent with the cone opsin changes, the cone transducin alpha-subunit mRNA decreased at both 4 and 8 weeks of age, whereas again the rod transducin alpha-subunit did not show any significant change. Rpe65(-/-) mice showed significant cone loss in both the central and ventral retina between 2 and 3 weeks of age. Administration of 9- or 11-cis retinal to Rpe65(-/-) mice 2 weeks of age increased cone density by twofold in these areas. CONCLUSIONS: In the Rpe65(-/-) mouse, the expression of cone-specific genes is downregulated and is accompanied by cone degeneration at early ages. Early administration of 9- or 11-cis retinal can partially prevent cone loss, suggesting that the absence of 11-cis chromophore may be responsible for the early cone degeneration.
机译:目的:RPE65对于11-顺式视网膜的生成至关重要。已知RPE65敲除(Rpe65(-/-))小鼠中的杆状感光细胞会随着年龄的增长而缓慢退化。这项研究旨在检查视锥细胞感光细胞和Rpe65(-/-)小鼠视锥细胞特异性基因的表达。方法:通过微阵列鉴定基因表达变化并通过实时RT-PCR确认。圆锥形感光体在平坦的视网膜中被花生凝集素(PNA)凝集素染色。 9或11顺式视网膜是通过腹膜内注射提供的。结果:短波(SWL)视锥蛋白mRNA在2周龄时显着下降,而中波(MWL)视锥蛋白mRNA下降则出现在年龄较晚。相反,视紫红质的mRNA水平在所有年龄段均未显示任何显着变化。与视锥蛋白的变化一致,视锥转导蛋白α-亚基mRNA在4和8周龄时均下降,而视杆转导蛋白α-亚基再次未显示任何显着变化。 Rpe65(-/-)小鼠在2至3周龄的中央和腹侧视网膜均显示出明显的视锥细胞丢失。 9周或11顺式视网膜的Rpe65(-/-)小鼠的管理2周龄使这些区域的视锥密度增加了两倍。结论:在Rpe65(-/-)小鼠中,视锥细胞特异性基因的表达被下调,并伴随着视锥细胞的退化。早期施用9-或11-顺式视网膜可部分预防视锥细胞丢失,提示缺乏11-顺式生色团可能是导致视锥细胞早期变性的原因。

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