A-synuclein Induces Microglial Cell Migration through Stimulating HIF-1 alpha Accumulation

作者：Qiao, Hongfei^*; He, Xijing; Zhang, Qiaojun; Zhang, Ni; Li, Libo; Hui, Yanping; Li, Wenjuan; Wang, Dong; Wu, Zhonghen

来源：Journal of Neuroscience Research, 2017, 95(9): 1809-1817.

DOI：10.1002/jnr.24012

• microglial cell
• spinal cord injury
• HIF-1 alpha
• toll-like receptor 7/8
• caveolin-1

Microglial cell migration and infiltration plays a critical role in spinal cord injury after thoracoabdominal aortic surgery. In our previous study, alpha-synuclein, a presynaptic protein was shown to be released from injured neurons and cause microglial cell activation. Here, we aimed to explore the effect of alpha-synuclein on microglial cell migration. Primary microglial cells were isolated from Sprague-Dawley rats and then exposed different doses (0.2, 0.4, and 0.6 mu M) of a-synuclein oligomers. The mRNA and protein levels of HIF-1 alpha were then analyzed by qRT-PCR and Western blot. Cell migration was examined by a 96-well Boyden chamber. Moreover, toll-like receptor (TLR) 2-expression as well as TLR7/8-expression was inhibited by specific siRNA transfection. HIF-1 alpha was overexpressed by Ad-HIF-1 alpha transfection. In the results, alpha-synuclein was found to stimulate HIF-1 alpha accumulation in microglial cells in a dose-dependent manner. Silencing HIF-1 alpha expression dampened alpha-synuclein induced microglial cell migration. Furthermore, blockade of TLR7/8 expression but not TLR2 expression reduced HIF-1 alpha accumulation in microglial cells. In addition, overexpressed HIF-1 alpha, along with Src, prompted caveolin-1 expression and phosphorylation, as well as migration in microglial cells. Asynuclein acts via TLR7/8 and enhances HIF-1 alpha expression, which might play a regulatory role in microglial cell migration.

• 出版日期2017-9
• 单位西安交通大学