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紫杉醇对从小鼠脑室下区培养的产后神经干细胞神经元分化的影响。

Effects of taxol on neuronal differentiation of postnatal neural stem cells cultured from mouse subventricular zone.

作者信息

Park Ki-Youb, Kim Seokyung, Kim Man Su

机构信息

Korea Science Academy of KAIST, 105-47 Baegyanggwanmun-ro, Busanjin-Gu, Busan, 614-100, South Korea.

Korea Science Academy of KAIST, 105-47 Baegyanggwanmun-ro, Busanjin-Gu, Busan, 614-100, South Korea.

出版信息

Differentiation. 2021 May-Jun;119:1-9. doi: 10.1016/j.diff.2021.03.001. Epub 2021 Apr 8.

DOI:10.1016/j.diff.2021.03.001
PMID:33848959
Abstract

Taxol (paclitaxel), a chemotherapeutic agent for several cancers, can adversely affect the peripheral nervous system. Recently, its negative impact on cognitive function in cancer patients has become evident. In rodents, taxol impaired learning and memory, with other possible negative effects on the brain. In this study, we investigated the effects of taxol on cultured neural stem cells (NSCs) from the mouse neurogenic region, the subventricular zone (SVZ). Taxol significantly decreased both proliferation and neuronal differentiation of NSCs. Transient treatment with taxol for one day during a 4-day differentiation greatly decreased neurogenesis along with an abnormal cell cycle progression. Yet, taxol did not kill differentiated Tuj1+ neurons and those neurons had longer neurites than neurons under control conditions. For glial differentiation, taxol significantly reduced oligodendrogenesis as observed by immunostaining for Olig2 and O4. However, differentiation of astrocytes was not affected by taxol. In contrast, differentiated oligodendrocytes were extremely sensitive to taxol. Almost no Olig2-positive cells were observed after three days of treatment with taxol. Taxol has distinct effects on neurons and glial cells during their production through differentiation from NSCs as well as post-differentiation. Thus, we suggest that taxol might interfere with neurogenesis of NSCs possibly through a disturbance in the cell cycle and may eliminate differentiated oligodendrocytes.

摘要

紫杉醇(泰素)是一种用于治疗多种癌症的化疗药物,它会对周围神经系统产生不利影响。最近,其对癌症患者认知功能的负面影响已变得明显。在啮齿动物中,紫杉醇会损害学习和记忆能力,并对大脑产生其他可能的负面影响。在本研究中,我们调查了紫杉醇对从小鼠神经发生区域脑室下区(SVZ)分离的培养神经干细胞(NSCs)的影响。紫杉醇显著降低了神经干细胞的增殖和神经元分化。在4天的分化过程中,用紫杉醇短暂处理一天会极大地减少神经发生,并伴有异常的细胞周期进程。然而,紫杉醇并未杀死分化的Tuj1 +神经元,并且这些神经元的神经突比对照条件下的神经元更长。对于胶质细胞分化,通过对Olig2和O4进行免疫染色观察到,紫杉醇显著减少了少突胶质细胞生成。然而,紫杉醇并未影响星形胶质细胞的分化。相比之下,分化的少突胶质细胞对紫杉醇极为敏感。用紫杉醇处理三天后,几乎未观察到Olig2阳性细胞。在神经干细胞通过分化产生神经元和胶质细胞的过程以及分化后,紫杉醇对它们具有不同的影响。因此,我们认为紫杉醇可能通过干扰细胞周期来干扰神经干细胞的神经发生,并可能消除分化的少突胶质细胞。

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