Department of Neurosurgery and Center for Neuroregeneration, Houston Methodist Research Institute, 6670 Bertner Avenue, Houston, TX, USA.
M.S. Biochemistry and Molecular Biology Program, Georgetown University, Washington D.C., USA.
Cell Mol Neurobiol. 2020 Oct;40(7):1199-1211. doi: 10.1007/s10571-020-00808-3. Epub 2020 Feb 14.
Serum amyloid A (SAA) is an acute phase protein upregulated in the liver after traumatic brain injury (TBI). So far, it has not been investigated whether SAA expression also occurs in the brain in response to TBI. For this, we performed a moderate controlled cortical impact injury in adult male and female mice and analyzed brain, blood, and liver samples at 6 h, 1, 3, and 10 days post-injury (dpi). We measured the levels of SAA in serum, brain and liver by western blot. We also used immunohistochemical techniques combined with in situ hybridization to determine SAA mRNA and protein expression in the brain. Our results revealed higher levels of SAA in the bloodstream in males compared to females at 6 h post-TBI. Liver and serum SAA protein showed a peak of expression at 1 dpi followed by a decrease at 3 to 10 dpi in both sexes. Both SAA mRNA and protein expression colocalize with astrocytes and macrophages/microglia in the cortex, corpus callosum, thalamus, and hippocampus after TBI. For the first time, here we show that SAA is expressed in the brain in response to TBI. Collectively, SAA expression was higher in males compared to females, and in association with the sex-dependent neuroinflammatory response after brain injury. We suggest that SAA could be a crucial protein associated to the acute neuroinflammation following TBI, not only for its hepatic upregulation but also for its expression in the injured brain.
血清淀粉样蛋白 A(SAA)是肝脏中创伤性脑损伤(TBI)后上调的急性期蛋白。到目前为止,还没有研究过 SAA 表达是否也会在大脑中对 TBI 产生反应。为此,我们在成年雄性和雌性小鼠中进行了中度控制性皮质撞击损伤,并在损伤后 6 h、1、3 和 10 天分析了大脑、血液和肝脏样本。我们通过 Western blot 测量了血清、大脑和肝脏中的 SAA 水平。我们还使用免疫组织化学技术结合原位杂交技术来确定大脑中的 SAA mRNA 和蛋白表达。我们的研究结果显示,TBI 后 6 h 雄性小鼠血液中的 SAA 水平高于雌性小鼠。肝和血清 SAA 蛋白在 1 dpi 时表达达到峰值,随后在 3 至 10 dpi 时在两性中均下降。在 TBI 后,SAA mRNA 和蛋白表达均与大脑皮质、胼胝体、丘脑和海马中的星形胶质细胞和巨噬细胞/小胶质细胞共定位。这是首次表明 SAA 在大脑中对 TBI 有反应时表达。总的来说,SAA 在雄性中的表达高于雌性,与脑损伤后性别依赖性神经炎症反应有关。我们认为,SAA 可能是与 TBI 后急性神经炎症相关的关键蛋白,不仅因为其肝脏上调,还因为其在受损大脑中的表达。