Differential gene expression profile analysis in corticosterone-treated PC12 cells

被引:0
|
作者
Zhao, Jing-Jie [1 ]
Zhang, Ping [2 ]
Li, Li [1 ]
Chen, Shu-Xing [3 ,5 ]
Joines, Allison [3 ]
Wu, Donald [3 ]
Wong, Megan [3 ]
Shahan, Justin [3 ]
Golden, Teresa [3 ]
Wu, Ning [3 ]
Li, Ming-Zhen [4 ]
机构
[1] Capital Med Univ, Beijing Friendship Hosp, Dept Tradit Chinese Med, Beijing, Peoples R China
[2] Beijing Ctr Phys & Chem Anal, Dept Res & Dev, Beijing, Peoples R China
[3] Southeastern Oklahoma State Univ, Dept Biol Sci, Durant, OK 74701 USA
[4] Shenzhen Ruipuxun Acad Stem Cell & Regenerat Med, Shenzhen, Peoples R China
[5] Henan Univ Sci & Technol, Sch Food & Bioengn, Luoyang 471023, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Corticosterone; PC12; cells; RNA-Seq; gene expression profiling; DISORDERS; AXIS; MECHANISMS; STRESS;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Major depressive disorder (MDD) is a highly prevalent psychiatric disorder that has been ranked as the 4th leading cause of disability worldwide. Past clinical and laboratory evidence has confirmed that abnormalities of the hypothalamic-pituitary-adrenal (HPA)-axis are involved in MDD development. In this study, we took advantage of corticosterone treatment of PC12 cells as a model to identify genes regulated by HPA-axis hormones. Next-generation RNA-Seq technology was utilized to explore genome-wide differentially expressed gene profiles between control and corticosterone treated PC12 cells. 1,274 genes with at least two-fold expression level change were identified. Gene ontology analysis showed that the top enriched biological processes included response to glucocorticoid signaling, apoptosis, cell division/DNA replication, and neuron projection/axon guidance, highly consistent with phenotypes of PC12 cells treated with corticosterone. Taken together, RNA-seq data is reliable and comprehensive, thus providing a valuable resource for understanding underlying mechanisms of glucocorticoid-induced neuron malfunction.
引用
收藏
页码:3097 / 3103
页数:7
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