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用于神经系统疾病的体细胞基因治疗。

Somatic gene therapy for nervous system disease.

作者信息

Tuszynski M H, Gage F H

机构信息

Department of Neuroscience, University of California at San Diego, La Jolla 92093, USA.

出版信息

Ciba Found Symp. 1996;196:85-94; discussion 94-7. doi: 10.1002/9780470514863.ch7.

Abstract

Neurotrophic factors are target-derived molecules that prevent neuronal degeneration during development and, in some cases, during adulthood. They offer substantial promise as therapeutic agents in neurological disease by preventing cell loss and promoting axonal regeneration. However, the optimal means of delivering neurotrophic factors to the nervous system, and the CNS in particular, is an unresolved issue. Neurotrophic factors rarely influence only a single target neuronal population, hence broad delivery of neurotrophic factors to the nervous system may results in effects on multiple non-targeted neuronal populations. Ideally, neurotrophin delivery to the nervous system should be target-specific, regionally restricted, chronic, safe, well-tolerated and of sufficient concentration to elicit responses from target neurons. In this paper we discuss the use of somatic gene transfer methods to deliver neurotrophic factors to the CNS in a manner that seeks to meet the above criteria.

摘要

神经营养因子是由靶细胞产生的分子,在发育过程中以及某些情况下在成年期可防止神经元变性。它们作为神经疾病的治疗剂具有巨大潜力,可防止细胞丢失并促进轴突再生。然而,将神经营养因子递送至神经系统,尤其是中枢神经系统的最佳方法仍是一个未解决的问题。神经营养因子很少仅影响单一的靶神经元群体,因此将神经营养因子广泛递送至神经系统可能会对多个非靶神经元群体产生影响。理想情况下,将神经营养蛋白递送至神经系统应具有靶特异性、区域限制性、长期性、安全性、良好耐受性且浓度足以引发靶神经元的反应。在本文中,我们讨论了使用体细胞基因转移方法以试图满足上述标准的方式将神经营养因子递送至中枢神经系统。

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