Upregulation of CXCR4 favoring neural-like cells migration via AKT activation

被引:20
作者
Li, Shiyong [1 ,2 ]
Deng, Liying [3 ]
Gong, Limin [3 ]
Bian, Hetao [3 ]
Dai, Yucheng [1 ]
Wang, Ye [3 ]
机构
[1] Nanchang Univ, Affiliated Hosp 2, Key Lab Mol Med, Nanchang City, Peoples R China
[2] Nanchang Univ, Affiliated Hosp 2, Dept Bone Surg, Nanchang City, Peoples R China
[3] Nanchang Univ, Affiliated Hosp 2, Dept Neurol, Nanchang City, Peoples R China
基金
中国国家自然科学基金;
关键词
AKT; SDF-1; alpha; CXCR4; Migration; BMSCs; MARROW STROMAL CELLS; BONE-MARROW; PROGENITOR CELLS; CHEMOKINE RECEPTORS; EXPRESSION; STROKE; DIFFERENTIATION; RAT; CHEMOTAXIS; THERAPY;
D O I
10.1016/j.neures.2010.04.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Stromal cell-derived factor-1 alpha (SDF-1 alpha) and its chemokine receptor 4 (CXCR4) play an important role in regulating bone marrow stromal stem cells (BMSCs) migration, proliferation and differentiation. The aim of this study is to investigate the expression of CXCR4 receptor and related mechanisms involved in neural-like cells migration. Results demonstrated that BMSCs were successfully induced to differentiate into neural-like cells, as early as 6 h after the initiation of neural differentiation, as revealed by both RT-PCR and immunocytochemistry. Interestingly, neuronal induction media (NIM) increased CXCR4 expression via Akt activation, which resulted in the increased ability of migration toward SDE-1 alpha in neural-like cells. Furthermore, we showed that migration toward SDF-1 was attenuated by AMD3100 (specific inhibitor of CXCR4) and Phosphatidylinositol 3-kinase (PI3K) inhibitor LY294002. These data suggest that the PI3K/Akt signaling pathway activated by NIM enhances migration of neural-like cells toward SDF-1 alpha though upregulation of CXCR4. This finding presents opportunities to develop new therapeutic strategies for the treatment of CNS disorders. (C) 2010 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:293 / 299
页数:7
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