School of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, USA.
Department of Translational Neuroscience, Barrow Neurological Institute, Phoenix, AZ, USA.
Acta Neuropathol Commun. 2023 Aug 22;11(1):137. doi: 10.1186/s40478-023-01625-7.
Traumatic brain injury (TBI) initiates tissue and cellular damage to the brain that is immediately followed by secondary injury sequalae with delayed and continual damage. This secondary damage includes pathological processes that may contribute to chronic neurodegeneration and permanent functional and cognitive deficits. TBI is also associated with an increased risk of developing neurodegenerative diseases such as Alzheimer's disease (AD), frontotemporal dementia (FTD), and amyotrophic lateral sclerosis (ALS) as indicated by shared pathological features. For example, abnormalities in the TAR DNA-binding Protein 43 (TDP-43) that includes cytoplasmic mislocalization, cytosolic aggregation, and an increase in phosphorylation and ubiquitination are seen in up to 50% of FTD cases, up to 70% of AD cases, and is considered a hallmark pathology of ALS occurring in > 97% of cases. Yet the prevalence of TDP-43 pathology post-TBI has yet to be fully characterized. Here, we employed a non-transgenic murine controlled cortical injury model of TBI and observed injury-induced hallmark TDP-43 pathologies in brain and spinal cord tissue distal to the primary injury site and did not include the focally damaged tissue within the primary cortical injury site. Analysis revealed a temporal-dependent and significant increase in neuronal TDP-43 mislocalization in the cortical forebrain rostral to and distant from the primary injury site up to 180 days post injury (DPI). TDP-43 mislocalization was also detected in neurons located in the ventral horns of the cervical spinal cord following a TBI. Moreover, a cortical layer-dependent affect was identified, increasing from superficial to deeper cortical layers over time from 7 DPI up to 180 DPI. Lastly, RNAseq analysis confirmed an injury-induced misregulation of several key biological processes implicated in neurons that increased over time. Collectively, this study demonstrates a connection between a single moderate TBI event and chronic neurodegenerative processes that are not limited to the primary injury site and broadly distributed throughout the cortex and corticospinal tract.
创伤性脑损伤(TBI)会立即引发脑部组织和细胞损伤,随后会出现继发性损伤后遗症,导致延迟和持续的损伤。这种继发性损伤包括可能导致慢性神经退行性变和永久性功能及认知缺陷的病理过程。TBI 还与神经退行性疾病(如阿尔茨海默病(AD)、额颞叶痴呆(FTD)和肌萎缩侧索硬化症(ALS))的风险增加有关,这是由共同的病理特征表明的。例如,TAR DNA 结合蛋白 43(TDP-43)的异常包括细胞质定位异常、细胞质聚集以及磷酸化和泛素化增加,在高达 50%的 FTD 病例、高达 70%的 AD 病例中可见,被认为是发生在超过 97%病例中的 ALS 的标志性病理学改变。然而,TBI 后 TDP-43 病理学的患病率尚未得到充分描述。在这里,我们采用了一种非转基因小鼠的皮质控制损伤模型 TBI,并观察到损伤诱导的标志性 TDP-43 病理学在原发性损伤部位远端的脑和脊髓组织中,不包括原发性皮质损伤部位内的局灶性损伤组织。分析显示,TDP-43 在皮质前脑的神经元向原发性损伤部位的近端和远端的定位异常在损伤后 180 天(DPI)时有时间依赖性和显著增加。在 TBI 后,TDP-43 也在颈椎脊髓腹角的神经元中被检测到。此外,还确定了一个皮质层依赖性的影响,即从 7 DPI 到 180 DPI,随着时间的推移,从浅层到深层皮质层逐渐增加。最后,RNAseq 分析证实,损伤诱导的几个关键生物学过程的异常调节随着时间的推移而增加。总之,这项研究表明,单次中度 TBI 事件与慢性神经退行性过程之间存在联系,这些过程不仅局限于原发性损伤部位,而且广泛分布于整个大脑皮层和皮质脊髓束。