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Microarray Analysis of mRNA and MicroRNA Expression Profile Reveals the Role of ß -Sitosterol-D-glucoside in the Proliferation of Neural Stem Cell.
Jiang, Li-Hua; Yang, Nian-Yun; Yuan, Xiao-Lin; Zou, Yi-Jie; Jiang, Ze-Qun; Zhao, Feng-Ming; Chen, Jian-Ping; Wang, Ming-Yan; Lu, Da-Xiang.
  • Jiang LH; Medical College of Jinan University, 601 Huangpu Road West, Guangzhou 510632, China.
  • Yang NY; Department of Pharmacognosy, Nanjing University of Chinese Medicine, Nanjing 210038, China.
  • Yuan XL; Basic Medical College of Nanjing University of Chinese Medicine, Nanjing 210038, China.
  • Zou YJ; Jiangsu Province Hospital of Traditional Chinese Medicine, Nanjing 210029, China.
  • Jiang ZQ; Basic Medical College of Nanjing University of Chinese Medicine, Nanjing 210038, China.
  • Zhao FM; Basic Medical College of Nanjing University of Chinese Medicine, Nanjing 210038, China.
  • Chen JP; Basic Medical College of Nanjing University of Chinese Medicine, Nanjing 210038, China.
  • Wang MY; Basic Medical College of Nanjing University of Chinese Medicine, Nanjing 210038, China.
  • Lu DX; Medical College of Jinan University, 601 Huangpu Road West, Guangzhou 510632, China.
Article en En | MEDLINE | ID: mdl-24391673
ABSTRACT
Neural stem cells (NSCs) are self-regenerating cells, but their regenerative capacity is limited. The present study was conducted to investigate the effect of ß -sitosterol-D-glucoside (BSSG) on the proliferation of hippocampal NSCs and to determine the corresponding molecular mechanism. Results of CCK-8 assay showed that BSSG significantly increased NSC proliferation and the effectiveness of BSSG was similar to that of basic fibroblast growth factor and epidermal growth factor. mRNA expression profiling showed that 960 genes were differentially expressed after NSCs were treated with BSSG. Among the 960 genes, IGF1 is considered as a key regulatory gene that functionally promotes NSC proliferation. MicroRNA (miRNA) expression profiling indicated that 30 and 84 miRNAs were upregulated and downregulated, respectively. miRNA-mRNA relevance analysis revealed that numerous mRNAs including IGF1 mRNA were negatively regulated by miRNAs with decreased expression, thereby increasing the corresponding mRNA expression. The increased expression of IGF1 protein was validated by ELISA. Picropodophyllin (PPP, an inhibitor of IGF-1R) inhibition test confirmed that the proliferation-enhancing effect depended on IGF1. This study provided information about BSSG as an efficient and inexpensive growth factor alternative, of which the effect is closely involved in IGF1.