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使用腺病毒载体将基因导入大鼠脑内。

Gene transfer into rat brain using adenoviral vectors.

作者信息

Thomas C E, Abordo-Adesida E, Maleniak T C, Stone D, Gerdes C A, Lowenstein P R

机构信息

University of Manchester, Manchester, United Kingdom.

出版信息

Curr Protoc Neurosci. 2001 May;Chapter 4:Unit 4.24. doi: 10.1002/0471142301.ns0424s13.

Abstract

Recombinant adenovirus vectors are attractive vehicles to deliver genes into the brain for the purposes of neurobiological research and for gene therapy of neurological diseases. This unit provides a comprehensive set of protocols for adenovirus vector-mediated gene transfer to the brain, including introduction of the vector into the brain by stereotaxic injection and preparation and processing of brain tissue for the evaluation of gene transfer. The potential side-effects of administering adenovirus vectors to the brain are discussed in detail. The unit also provides protocols for evaluating these side-effects (e.g., demyelination, inflammation, vector-mediated cytotoxicity, etc.). Finally, critical parameters for obtaining optimal gene transfer with minimum side-effects are presented.

摘要

重组腺病毒载体是将基因导入大脑的理想载体,可用于神经生物学研究以及神经疾病的基因治疗。本单元提供了一套全面的方案,用于腺病毒载体介导的基因向大脑的转移,包括通过立体定位注射将载体导入大脑,以及制备和处理脑组织以评估基因转移。详细讨论了向大脑施用腺病毒载体的潜在副作用。本单元还提供了评估这些副作用(如脱髓鞘、炎症、载体介导的细胞毒性等)的方案。最后,介绍了以最小副作用获得最佳基因转移的关键参数。

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