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首页> 外文期刊>Neurochemical Research >Effect of Intranigral Injection of GDNF and EGF on the Survival and Possible Differentiation Fate of Progenitors and Immature Neurons in 6-OHDA-Lesioned Rats
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Effect of Intranigral Injection of GDNF and EGF on the Survival and Possible Differentiation Fate of Progenitors and Immature Neurons in 6-OHDA-Lesioned Rats

机译:GDNF和EGF鼻内注射对6-OHDA损伤大鼠祖细胞和未成熟神经元存活和可能分化的影响

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We investigated the survival and the possible differentiation fate of the progenitors and immature neurons in the pars compacta of the substantia nigra (SNc) by intranigral injection of a glial cell line-derived neurotropic factor (GDNF) or glial cell line-derived neurotropic factor plus epidermal growth factor (EGF + GDNF) in 6-hydroxydopamine (6-OHDA)-lesioned rats. First, we performed behavioral tests by postural asymmetry and forelimb akinesia on the rats injected with 6-OHDA in striatum at day 7, and selected the qualified model according to the results. Then, intranigral GDNF or EGF + GDNF treatment was administered in the qualified PD model rats. On day 21, behavioral tests were performed with these rats; and then the rats were sacrificed for analyses of β-tubulin isotype-III (Tuj1), nestin, glial fibrillary acidic protein (GFAP), and tyrosine hydroxylase (TH) by immunohistochemistry and Western blotting. The results indicated that GDNF could promote the survival of the progenitor cells and immature neurons in rat SNc following 6-OHDA lesion. Moreover, EGF is capable of enhancing the survival effect of GDNF on the progenitor cells and immature neurons in SNc. On day 21, rapid functional recovery from the lesion-induced behavioral asymmetries was observed in the GDNF or EGF + GDNF-treated rats, and the numbers of TH-positive neurons increased in SNc, suggesting that the rats might generate new dopaminergic neurons. Thus, our study provides the new insight that the progenitors and immature neurons in SNc of 6-OHDA-lesioned rats might be able to differentiate toward the dopaminergic neurons fate subsequent to treatment with GDNF or EGF + GDNF.
机译:我们通过鼻内注射神经胶质细胞源性神经胶质细胞因子(GDNF)或神经胶质细胞系神经质因子加鼻内注射,研究了黑质(SNc)致密部致密细胞中祖细胞和未成熟神经元的存活和可能分化的命运。表皮生长因子(EGF + GDNF)在6-羟基多巴胺(6-OHDA)损伤的大鼠中。首先,我们在第7天通过姿势不对称和前肢运动障碍对纹状体中注射了6-OHDA的大鼠进行了行为测试,并根据结果选择了合格的模型。然后,对合格的PD模型大鼠进行鼻内GDNF或EGF + GDNF治疗。在第21天,对这些大鼠进行了行为测试;然后处死大鼠,通过免疫组织化学和Western印迹法分析β-微管蛋白III型(Tuj1),巢蛋白,神经胶质纤维酸性蛋白(GFAP)和酪氨酸羟化酶(TH)。结果表明,GDNF可以促进6-OHDA损伤后大鼠SNc中祖细胞和未成熟神经元的存活。此外,EGF能够增强GDNF对SNc中祖细胞和未成熟神经元的存活作用。在第21天,在GDNF或EGF + GDNF处理的大鼠中,观察到了其从病变引起的行为不对称中快速恢复的功能,SNc中TH阳性神经元的数量增加,表明这些大鼠可能会产生新的多巴胺能神经元。因此,我们的研究提供了新的见解,即6-OHDA损伤大鼠的SNc中的祖细胞和未成熟神经元可能能够在用GDNF或EGF + GDNF治疗后向多巴胺能神经元分化。

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