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在精神疾病模型中,类人胶原蛋白对神经干细胞功能及其向脑内迁移能力的影响。

Effects of atelocollagen on neural stem cell function and its migrating capacity into brain in psychiatric disease model.

机构信息

Department of Neuropsychiatry, Sapporo Medical University, School of Medicine, S-1, W-16, Chuo-ku, Sapporo, 060-8543, Japan,

出版信息

J Neural Transm (Vienna). 2013 Oct;120(10):1491-8. doi: 10.1007/s00702-013-1010-4. Epub 2013 Apr 6.

Abstract

Stem cell therapy is well proposed as a potential method for the improvement of neurodegenerative damage in the brain. Among several different procedures to reach the cells into the injured lesion, the intravenous (IV) injection has benefit as a minimally invasive approach. However, for the brain disease, prompt development of the effective treatment way of cellular biodistribution of stem cells into the brain after IV injection is needed. Atelocollagen has been used as an adjunctive material in a gene, drug and cell delivery system because of its extremely low antigenicity and bioabsorbability to protect these transplants from intrabody environment. However, there is little work about the direct effect of atelocollagen on stem cells, we examined the functional change of survival, proliferation, migration and differentiation of cultured neural stem cells (NSCs) induced by atelocollagen in vitro. By 72-h treatment 0.01-0.05% atelocollagen showed no significant effects on survival, proliferation and migration of NSCs, while 0.03-0.05% atelocollagen induced significant reduction of neuronal differentiation and increase of astrocytic differentiation. Furthermore, IV treated NSCs complexed with atelocollagen (0.02%) could effectively migrate into the brain rather than NSC treated alone using chronic alcohol binge model rat. These experiments suggested that high dose of atelocollagen exerts direct influence on NSC function but under 0.03% of atelocollagen induces beneficial effect on regenerative approach of IV administration of NSCs for CNS disease.

摘要

干细胞疗法被广泛提出作为改善大脑神经退行性损伤的一种潜在方法。在将细胞递送到损伤部位的几种不同方法中,静脉内(IV)注射作为一种微创方法具有优势。然而,对于脑部疾病,需要迅速开发出有效的细胞生物分布方法,使干细胞在 IV 注射后进入大脑。明胶作为一种辅助材料,已被用于基因、药物和细胞递送系统,因为它具有极低的抗原性和生物可吸收性,可以保护这些移植体免受体内环境的影响。然而,关于明胶对干细胞的直接作用的研究很少,我们研究了明胶在体外对培养的神经干细胞(NSCs)的存活、增殖、迁移和分化功能的影响。经过 72 小时的 0.01-0.05%明胶处理,对 NSCs 的存活、增殖和迁移没有显著影响,而 0.03-0.05%明胶诱导神经元分化减少和星形胶质细胞分化增加。此外,用慢性酒精 binge 模型大鼠进行 IV 处理的与明胶(0.02%)结合的 NSCs 可以有效地迁移到大脑中,而单独用 NSCs 处理则不能。这些实验表明,高剂量的明胶对 NSC 功能有直接影响,但低于 0.03%的明胶对 IV 给予 NSCs 进行 CNS 疾病再生治疗有有益作用。

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