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NTPDase2 and the P2Y1 receptor are not required for mammalian eye formation

机译:不需要NTPDase2和P2Y1受体来形成哺乳动物的眼睛

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摘要

Eye formation in vertebrates is controlled by a conserved pattern of molecular networks. Homeobox transcription factors are crucially involved in the establishment and maintenance of the retina. A previous study of Massé et al. (Nature, 449: 1058–62, 2007) using morpholino knockdown identified the ectonucleotidase NTPDase2 and the P2Y1 receptor as essential elements for eye formation in embryos of the clawed frog Xenopus laevis. In order to investigate whether a similarly essential mechanism would be active in mammalian eye development, we analyzed mice KO for Entpd2 or P2ry1 as well as double KO for Entpd2/P2ry1. These mice developed normal eyes. In order to identify potential deficits in the molecular identity or in the arrangement of the cellular elements of the retina, we performed an immunohistological analysis using a variety of retinal markers. The analysis of single and double KO mice demonstrated that NTPDase2 and P2Y1 receptors are not required for murine eye formation, as previously shown for eye development in Xenopus laevis.
机译:脊椎动物的眼睛形成受分子网络的保守模式控制。同源盒转录因子在视网膜的建立和维持中至关重要。 Massé等人的先前研究。 (Nature,449:1058–62,2007)使用吗啉代敲低法鉴定了外切核苷酸酶NTPDase2和P2Y1受体是爪蟾Xenopus laevis胚胎眼形成的必要元素。为了研究类似的基本机制在哺乳动物眼发育中是否具有活性,我们对Entpd2或P2ry1的小鼠KO以及Entpd2 / P2ry1的双重KO进行了分析。这些小鼠的眼睛正常。为了识别分子身份或视网膜细胞元素排列中的潜在缺陷,我们使用了多种视网膜标记物进行了免疫组织学分析。对单只和双只KO小鼠的分析表明,鼠眼的形成不需要NTPDase2和P2Y1受体,如先前在非洲爪蟾眼中的发育所示。

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