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基因工程神经干细胞治疗神经系统疾病;最新进展

Genetically engineered neural stem cells (NSCs) therapy for neurological diseases; state-of-the-art.

作者信息

Lutfi Ismaeel Ghufran, Makki AlHassani Olfet Jabbar, S Alazragi Reem, Hussein Ahmed Ammar, H Mohamed Asma'a, Yasir Jasim Nisreen, Hassan Shari Falah, Almashhadani Haider Abdulkareem

机构信息

Department of Pharmacology, College of Pharmacy, University of Al-Ameed, Karbala, Iraq.

Department of Clinical Laboratory Sciences, College of Pharmacy, University of Al-Ameed, Karbala, Iraq.

出版信息

Biotechnol Prog. 2023 Sep-Oct;39(5):e3363. doi: 10.1002/btpr.3363. Epub 2023 May 23.

Abstract

Neural stem cells (NSCs) are multipotent stem cells with remarkable self-renewal potential and also unique competencies to differentiate into neurons, astrocytes, and oligodendrocytes (ODCs) and improve the cellular microenvironment. In addition, NSCs secret diversity of mediators, including neurotrophic factors (e.g., BDNF, NGF, GDNF, CNTF, and NT-3), pro-angiogenic mediators (e.g., FGF-2 and VEGF), and anti-inflammatory biomolecules. Thereby, NSCs transplantation has become a reasonable and effective treatment for various neurodegenerative disorders by their capacity to induce neurogenesis and vasculogenesis and dampen neuroinflammation and oxidative stress. Nonetheless, various drawbacks such as lower migration and survival and less differential capacity to a particular cell lineage concerning the disease pathogenesis hinder their application. Thus, genetic engineering of NSCs before transplantation is recently regarded as an innovative strategy to bypass these hurdles. Indeed, genetically modified NSCs could bring about more favored therapeutic influences post-transplantation in vivo, making them an excellent option for neurological disease therapy. This review for the first time offers a comprehensive review of the therapeutic capability of genetically modified NSCs rather than naïve NSCs in neurological disease beyond brain tumors and sheds light on the recent progress and prospect in this context.

摘要

神经干细胞(NSCs)是具有显著自我更新潜能的多能干细胞,还具有分化为神经元、星形胶质细胞和少突胶质细胞(ODCs)以及改善细胞微环境的独特能力。此外,神经干细胞分泌多种介质,包括神经营养因子(如脑源性神经营养因子、神经生长因子、胶质细胞源性神经营养因子、睫状神经营养因子和神经营养素-3)、促血管生成介质(如成纤维细胞生长因子-2和血管内皮生长因子)以及抗炎生物分子。因此,神经干细胞移植凭借其诱导神经发生和血管生成以及减轻神经炎症和氧化应激的能力,已成为治疗各种神经退行性疾病的合理且有效方法。尽管如此,诸如迁移和存活率较低以及针对疾病发病机制向特定细胞谱系的分化能力较弱等各种缺点阻碍了它们的应用。因此,移植前对神经干细胞进行基因工程改造最近被视为克服这些障碍的创新策略。事实上,基因修饰的神经干细胞在体内移植后可带来更有利的治疗效果,使其成为神经疾病治疗的理想选择。本综述首次全面回顾了基因修饰的神经干细胞而非未处理的神经干细胞在脑肿瘤以外的神经疾病中的治疗能力,并阐明了这方面的最新进展和前景。

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