Suppression of MicroRNA let-7a Expression by Agmatine Regulates Neural Stem Cell Differentiation

被引:10
作者
Song, Juhyun [1 ]
Oh, Yumi [1 ,2 ,3 ]
Kim, Jong Youl [1 ]
Cho, Kyoung Joo [1 ,2 ,3 ]
Lee, Jong Eun [1 ,2 ,3 ]
机构
[1] Yonsei Univ, Coll Med, Dept Anat, Seoul, South Korea
[2] Yonsei Univ, Coll Med, Brain Korea Plus Project Med Sci 21, Seoul, South Korea
[3] Yonsei Univ, Coll Med, Brain Res Inst, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Neural stem cell (NSCs); microRNA let-7a (let-7a); agmatine; DCX; TLX; ERK; SUBVENTRICULAR ZONE; SELF-RENEWAL; RETROVIRAL EXPRESSION; ADULT NEUROGENESIS; IN-VITRO; NEURONS; PATHWAY; BRAIN; RECEPTOR; PROLIFERATION;
D O I
10.3349/ymj.2016.57.6.1461
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: Neural stem cells (NSCs) effectively reverse some severe central nervous system (CNS) disorders, due to their ability to differentiate into neurons. Agmatine, a biogenic amine, has cellular protective effects and contributes to cellular proliferation and differentiation in the CNS. Recent studies have elucidated the function of microRNA let-7a (let-7a) as a regulator of cell differentiation with roles in regulating genes associated with CNS neurogenesis. Materials and Methods: This study aimed to investigate whether agmatine modulates the expression of crucial regulators of NSC differentiation including DCX, TLX, c-Myc, and ERK by controlling let-7a expression. Results: Our data suggest that high levels of let-7a promoted the expression of TLX and c-Myc, as well as repressed DCX and ERK expression. In addition, agmatine attenuated expression of TLX and increased expression of ERK by negatively regulating let-7a. Conclusion: Our study therefore enhances the present understanding of the therapeutic potential of NSCs in CNS disorders.
引用
收藏
页码:1461 / 1467
页数:7
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