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微小RNA家族对涡虫大脑和视觉系统的再生至关重要。

The family of microRNAs is crucial for regeneration of the brain and visual system in the planarian .

作者信息

Sasidharan Vidyanand, Marepally Srujan, Elliott Sarah A, Baid Srishti, Lakshmanan Vairavan, Nayyar Nishtha, Bansal Dhiru, Sánchez Alvarado Alejandro, Vemula Praveen Kumar, Palakodeti Dasaradhi

机构信息

Institute for Stem Cell Biology and Regenerative Medicine, GKVK campus, Bangalore, Karnataka 560065, India.

Manipal University, Manipal, Karnataka 576104, India.

出版信息

Development. 2017 Sep 15;144(18):3211-3223. doi: 10.1242/dev.144758. Epub 2017 Aug 14.

Abstract

Brain regeneration in planarians is mediated by precise spatiotemporal control of gene expression and is crucial for multiple aspects of neurogenesis. However, the mechanisms underpinning the gene regulation essential for brain regeneration are largely unknown. Here, we investigated the role of the family of microRNAs in planarian brain regeneration. The family () is highly conserved in animals and regulates neurogenesis by facilitating neural differentiation, yet its role in neural wiring and brain organization is not known. We developed a novel method for delivering anti-miRs using liposomes for the functional knockdown of microRNAs. knockdown revealed a key role for these microRNAs in neuronal organization during planarian brain regeneration. Our results also demonstrated an essential role for in the generation of eye progenitors. Additionally, regulates , which encodes an axon guidance protein, either by targeting mRNA or, potentially, by modulating the canonical Notch pathway. Together, our results reveal a role for in regulating the regeneration of a functional brain and visual system.

摘要

涡虫的脑再生由基因表达的精确时空控制介导,对神经发生的多个方面至关重要。然而,脑再生所必需的基因调控的基础机制在很大程度上尚不清楚。在这里,我们研究了微小RNA家族在涡虫脑再生中的作用。该微小RNA家族()在动物中高度保守,并通过促进神经分化来调节神经发生,但其在神经连接和脑组织结构中的作用尚不清楚。我们开发了一种使用脂质体递送抗微小RNA以实现微小RNA功能敲低的新方法。敲低揭示了这些微小RNA在涡虫脑再生过程中神经元组织中的关键作用。我们的结果还证明了在眼祖细胞产生中的重要作用。此外,通过靶向mRNA或可能通过调节经典Notch途径来调节,后者编码一种轴突导向蛋白。总之,我们的结果揭示了在调节功能性脑和视觉系统再生中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c11/5612250/8f3a13b7c6ae/develop-144-144758-g1.jpg

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