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

Microglial cell migration and infiltration plays a critical role in spinal cord injury after thoracoabdominal aortic surgery. In our previous study, a-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 a-synuclein on microglial cell migration. Primary microglial cells were isolated from Sprague–Dawley rats and then exposed different doses (0.2, 0.4, and 0.6lM) of a-synuclein oligomers. The mRNA and protein levels of HIF-1a 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-1a was overexpressed by AdHIF-1a transfection. In the results, a-synuclein was found to stimulate HIF-1a accumulation in microglial cells in a dose-dependent manner. Silencing HIF-1a expression dampened a-synuclein induced microglial cell migration. Furthermore, blockade of TLR7/8 expression but not TLR2 expression reduced HIF-1a accumulation in microglial cells. In addition, overexpressed HIF-1a, along with Src, prompted caveolin-1 expression and phosphorylation, as well as migration in microglial cells. Asynuclein acts via TLR7/8 and enhances HIF-1a expression, which might play a regulatory role in microglial cell migration. VC 2017 Wiley Periodicals, Inc.