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斑马鱼 RNase 的催化活性和分泌对于其在运动神经元和脉管系统中的体内功能至关重要。

The catalytic activity and secretion of zebrafish RNases are essential for their in vivo function in motor neurons and vasculature.

机构信息

Department of Biology and Biochemistry, University of Bath, Bath, BA2 7AY, UK.

Division of Biological Sciences and Bond Life Sciences Center, University of Missouri, Columbia, MO, 65211-7310, USA.

出版信息

Sci Rep. 2019 Feb 1;9(1):1107. doi: 10.1038/s41598-018-37140-2.

Abstract

Angiogenin (hANG), a member of the Ribonuclease A superfamily has angiogenic, neurotrophic and neuroprotective activities. Mutations in hANG have been found in patients with Amyotrophic lateral sclerosis (ALS). The zebrafish (Danio rerio) rnasel-1, 2 and 3 are orthologues of hANG and of these only Rnasel-1 and Rnasel-2 have been shown to be angiogenic. Herein we show that NCI-65828, a potent and specific small molecule inhibitor of hANG inhibits Rnasel-1 to a similar extent. Treatment of early zebrafish embryos with NCI-65828, or with terrein, a fungal metabolite which prevents the secretion of hANG, resulted in spinal neuron aberrations as well defects in trunk vasculature. Our detailed expression analysis and inhibitor studies suggest that Rnasel-1 plays important roles in neuronal migration and pathfinding as well as in angiogenesis in zebrafish. Our studies suggest the usefulness of the zebrafish as a model to dissect the molecular consequences of the ANG ALS variants.

摘要

血管生成素(hANG)是核糖核酸酶 A 超家族的一员,具有血管生成、神经营养和神经保护作用。在肌萎缩侧索硬化症(ALS)患者中发现了 hANG 的突变。斑马鱼(Danio rerio)的 rnasel-1、2 和 3 是 hANG 的同源物,其中只有 Rnasel-1 和 Rnasel-2 被证明具有血管生成作用。本文显示,NCI-65828 是 hANG 的一种有效且特异性的小分子抑制剂,对 Rnasel-1 的抑制作用相似。用 NCI-65828 或真菌代谢产物 terrein 处理早期斑马鱼胚胎,terrein 可阻止 hANG 的分泌,导致脊髓神经元异常以及躯干血管缺陷。我们的详细表达分析和抑制剂研究表明,Rnasel-1 在斑马鱼的神经元迁移和寻路以及血管生成中发挥重要作用。我们的研究表明,斑马鱼作为一种模型可用于剖析 ANG ALS 变体的分子后果。

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