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通过电穿孔导入CAS9蛋白-gRNA复合物对蝾螈脊髓神经干细胞进行直接基因敲除

Direct Gene Knock-out of Axolotl Spinal Cord Neural Stem Cells via Electroporation of CAS9 Protein-gRNA Complexes.

作者信息

Lou Wilson Pak-Kin, Wang Liqun, Long Cheng, Liu Lei, Fei Ji-Feng

机构信息

School of Life Sciences, South China Normal University; The Research Institute of Molecular Pathology (IMP), Vienna Biocenter (VBC).

Institute for Brain Research and Rehabilitation (IBRR), South China Normal University.

出版信息

J Vis Exp. 2019 Jul 9(149). doi: 10.3791/59850.

Abstract

The axolotl has the unique ability to fully regenerate its spinal cord. This is largely due to the ependymal cells remaining as neural stem cells (NSCs) throughout life, which proliferate to reform the ependymal tube and differentiate into lost neurons after spinal cord injury. Deciphering how these NSCs retain pluripotency post-development and proliferate upon spinal cord injury to reform the exact pre-injury structure can provide valuable insight into how mammalian spinal cords may regenerate as well as potential treatment options. Performing gene knock-outs in specific subsets of NSCs within a restricted time period will allow study of the molecular mechanisms behind these regenerative processes, without being confounded by development perturbing effects. Described here is a method to perform gene knock-out in axolotl spinal cord NSCs using the CRISPR-Cas9 system. By injecting the CAS9-gRNA complex into the spinal cord central canal followed by electroporation, target genes are knocked out in NSCs within specific regions of the spinal cord at a desired timepoint, allowing for molecular studies of spinal cord NSCs during regeneration.

摘要

美西螈具有完全再生其脊髓的独特能力。这主要归功于室管膜细胞在其一生中都保持为神经干细胞(NSCs),在脊髓损伤后,这些细胞会增殖以重新形成室管膜管,并分化为丢失的神经元。弄清楚这些神经干细胞如何在发育后保持多能性以及在脊髓损伤时增殖以重新形成确切的损伤前结构,能够为哺乳动物脊髓如何再生以及潜在的治疗方案提供有价值的见解。在特定时间段内在神经干细胞的特定亚群中进行基因敲除,将有助于研究这些再生过程背后的分子机制,而不会受到发育干扰效应的混淆。本文描述了一种使用CRISPR-Cas9系统在美西螈脊髓神经干细胞中进行基因敲除的方法。通过将CAS9-gRNA复合物注入脊髓中央管,随后进行电穿孔,可在所需时间点在脊髓特定区域的神经干细胞中敲除靶基因,从而能够对再生过程中的脊髓神经干细胞进行分子研究。

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