Department of Neurology, Brigham and Women's Hospital, Boston, MA 02115, USA.
Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, 149 13th Street, Charlestown, MA 02119, USA.
Int J Mol Sci. 2021 Jan 18;22(2):907. doi: 10.3390/ijms22020907.
Repetitive closed head injury (rCHI) is commonly encountered in young athletes engaged in contact and collision sports. Traumatic brain injury (TBI) including rCHI has been reported to be an important risk factor for several tauopathies in studies of adult humans and animals. However, the link between rCHI and the progression of tau pathology in adolescents remains to be elucidated. We evaluated whether rCHI can trigger the initial acceleration of pathological tau in adolescent mice and impact the long-term outcomes post-injury. To this end, we subjected adolescent transgenic mice expressing the P301S tau mutation to mild rCHI and assessed tau hyperphosphorylation, tangle formation, markers of neuroinflammation, and behavioral deficits at 40 days post rCHI. We report that rCHI did not accelerate tau pathology and did not worsen behavioral outcomes compared to control mice. However, rCHI induced cortical and hippocampal microgliosis and corpus callosum astrocytosis in P301S mice by 40 days post-injury. In contrast, we did not find significant microgliosis or astrocytosis after rCHI in age-matched WT mice or sham-injured P301S mice. Our data suggest that neuroinflammation precedes the development of Tau pathology in this rCHI model of adolescent repetitive mild TBI.
重复性闭合性颅脑损伤(rCHI)在从事接触性和碰撞性运动的年轻运动员中很常见。研究表明,创伤性脑损伤(TBI)包括 rCHI,是成人和动物研究中几种tau 病的重要危险因素。然而,rCHI 与青少年 tau 病理进展之间的联系仍有待阐明。我们评估了 rCHI 是否会引发青少年小鼠中病理性 tau 的初始加速,并影响损伤后的长期结果。为此,我们使表达 P301S tau 突变的青春期转基因小鼠经受轻度 rCHI,并在 rCHI 后 40 天评估 tau 过度磷酸化、缠结形成、神经炎症标志物和行为缺陷。我们报告说,与对照小鼠相比,rCHI 并未加速 tau 病理,也未恶化行为结果。然而,rCHI 在损伤后 40 天诱导了 P301S 小鼠的皮质和海马小胶质细胞增生和胼胝体星形胶质细胞增生。相比之下,我们在年龄匹配的 WT 小鼠或假损伤 P301S 小鼠中 rCHI 后没有发现明显的小胶质细胞增生或星形胶质细胞增生。我们的数据表明,神经炎症先于这个青少年重复性轻度 TBI rCHI 模型中 Tau 病理的发展。