Journal
JOURNAL OF NEUROSCIENCE RESEARCH
Volume 95, Issue 9, Pages 1809-1817Publisher
WILEY
DOI: 10.1002/jnr.24012
Keywords
microglial cell; spinal cord injury; HIF-1 alpha; toll-like receptor 7/8; caveolin-1
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Funding
- Scientific Research Foundation of the Second Affiliated Hospital of Xi'an Jiaotong University YJ [ZD201206]
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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. (C) 2017 Wiley Periodicals, Inc.
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