Stigmasterol promotes neuronal migration via reelin signaling in neurosphere migration assays

被引:12
作者
Haque, Md. Nazmul [1 ]
Moon, Il Soo [1 ]
机构
[1] Dongguk Univ, Grad Sch Med, Dept Anat, 123 Dongdae Ro, Gyeongju 38066, South Korea
基金
新加坡国家研究基金会;
关键词
Dynein; JNK signaling; molecular docking; neurosphere migration assay; Reln; stigmasterol; GENETIC CLASSIFICATION; NEURITE EXTENSION; PLANT STEROLS; RECEPTOR; MALFORMATIONS; DOUBLECORTIN; CENTROSOME; APOER2; BRAIN; LIS1;
D O I
10.1080/1028415X.2018.1544970
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Stigmasterol (ST) is a multifunctional phytosterol and is found in diverse food. In our previous transcriptomics study, we found ST upregulated migration-related genes. In the present study, we carried outin vitroneurosphere migration assays to investigate the effects of ST on neuronal migration. For this purpose, neurospheres were produced by culturing rat (Sprague-Dawley) E14 cortical neurons. The addition of ST (75 mu M) to culture medium increased not only the numbers of migratory neurons by 15% but the distance of movement up to 120 mu m from the centers of neurospheres as compared to vehicle cultures. Immunocytochemistry and immunoblotting showed ST upregulated the expressions of Reelin (Reln) and its downstream signaling molecules like phospho-JNK (c-Jun N-terminal kinase), doublecortin (DCX) and dynein heavy chain (DHC) in migratory neurons. Furthermore,in silicomolecular docking simulation indicated that ST interacts with Relin receptor ApoER2 by forming a hydrogen bond with Lys2467 and other van der Waals interactions. Taken together, our study shows that ST upregulates Reln signaling and promotes neuronal migration and suggests that ST supplementation is considered as a potential means of treating migration-related CNS disorders.
引用
收藏
页码:679 / 687
页数:9
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