Fang Huang, Song PeiWen, Shen CaiLiang, Liu XiaoYing, Li HaiTai
a Department of Spinal Surgery , The First Affiliated Hospital of Anhui Medical University , Hefei , China.
b School of Life Science, Anhui Medical University , Heifei , China.
Neurol Res. 2016 Nov;38(11):965-972. doi: 10.1080/01616412.2016.1232549. Epub 2016 Sep 16.
In this study, we aimed to investigate the effect of bone mesenchymal stem cells (BMSCs) conditioned medium on BMP4-induced activation of the Smad signaling pathway during the process of neural stem cells differentiation.
We designed four experimental groups: (A) control group, (B) BMP-4 treatment group, (C) BMSC-CM group, and (D) BMSC-CM (BMSC-conditioned medium) combined with BMP-4 group. The expression of microtube-associated protein-2 (MAP-2) detected by immunocytochemical staining and western blot. The expression of glial fibrillary acidic protein (GFAP) and BMP receptors (BMPRII and BMPRIa) was determined by western blot, while SMAD1/5/8 and SMAD6 mRNA expression was detected by quantitative real-time polymerase chain reaction (Q-RT-PCR).
We found that the expression of microtube-associated protein-2 (MAP-2) increased in group B compared to group A. In group C, the expression of GFAP was increased and the expression of MAP-2 was decreased compared to group A. This phenomenon was weaker in group D. We also demonstrated that BMSC-CM could inhibit the activation of BMP signaling by downregulating the expression of BMPRII and BMPRIa proteins. Moreover, BMSC-CM could upregulate the expression of Smad6 mRNA and inhibit the activation of Smad1/5/8 mRNA.
These observations suggest that BMSC-CM could neutralize the effect of BMP-4 on the differentiation of NSCs by upregulating the expression of Smad6 and decrease the expression of GFAP by inhibiting the BMP-4-SMAD1/5/8 signaling pathway, conversely increasing the generation of neurons.
在本研究中,我们旨在探讨骨间充质干细胞(BMSCs)条件培养基对神经干细胞分化过程中BMP4诱导的Smad信号通路激活的影响。
我们设计了四个实验组:(A)对照组,(B)BMP - 4处理组,(C)BMSC - CM组,以及(D)BMSC - CM(BMSC条件培养基)联合BMP - 4组。通过免疫细胞化学染色和蛋白质免疫印迹法检测微管相关蛋白 - 2(MAP - 2)的表达。通过蛋白质免疫印迹法测定胶质纤维酸性蛋白(GFAP)和BMP受体(BMPRII和BMPRIa)的表达,而通过定量实时聚合酶链反应(Q - RT - PCR)检测SMAD1/5/8和SMAD6 mRNA的表达。
我们发现,与A组相比,B组中微管相关蛋白 - 2(MAP - 2)的表达增加。与A组相比,C组中GFAP的表达增加而MAP - 2的表达降低。D组中这种现象较弱。我们还证明,BMSC - CM可通过下调BMPRII和BMPRIa蛋白的表达来抑制BMP信号的激活。此外,BMSC - CM可上调Smad6 mRNA的表达并抑制Smad1/5/8 mRNA的激活。
这些观察结果表明,BMSC - CM可通过上调Smad6的表达来抵消BMP - 4对神经干细胞分化的影响,并通过抑制BMP - 4 - SMAD1/5/8信号通路来降低GFAP的表达,从而反过来增加神经元的生成。