分子生物学
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细胞培养与分析
蛋白研究
细胞因子
重组蛋白
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高通量测序建库
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抑制剂激活剂与常用试剂
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β-amyloid increases neurocan expression through regulating Sox9 in astrocytes: A potential relationship between Sox9 and chondroitin sulfate proteoglycans in Alzheimer's disease

Han Yan, Xiaolong Zhu, Junchao Xie, Yanxin Zhao, Xueyuan Liu

Journal:BRAIN RESEARCH

IF:2.56

DOI:10.1016/j.brainres.2016.06.010

PMID:27317830

Published:2016-06-16

research field:神经科学分子生物学神经退行性疾病

Abstract

Objective This study aimed to investigate whether β-amyloid (Aβ) was able to enhance neurocan expression in a Sox9 dependent manner in astrocytes. Methods and materials Astrocytes were incubated with Aβ at different concentrations, the expression of Sox9 and neurocan was detected by Western blot assay. Meanwhile, the viability and proliferation of astrocytes were assessed by MTT assay . Then, the Sox9 expression was silenced, and the expression of Sox9 and neurocan was examined. Results After incubation with Aβ, the viability of astrocytes was increased regardless silencing of Sox9 (all P<0.05). The proliferation of astrocytes was also gradually increased with the increase in the time of Aβ incubation (all P<0.05). With the increase in Aβ concentration, the expression of Sox9 and neurocan was also increased (all P<0.05). However, after silencing of Sox9 expression, the neurocan expression was significantly reduced as compared to control group and scra-siRNA group (all P<0.05). Conclusion Our study shows the viability and proliferation of astrocytes are significantly increased by Aβ in a dose dependent manner. Moreover, Aβ may effectively up-regulate the neurocan expression via regulating Sox9.

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