创伤性脑损伤在非转基因小鼠原发损伤部位远端组织中诱导TDP-43错位和神经退行性作用。

IF 6.2 2区 医学 Q1 NEUROSCIENCES
George R Bjorklund, Jennifer Wong, David Brafman, Robert Bowser, Sarah E Stabenfeldt
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引用次数: 0

摘要

创伤性脑损伤(TBI)引发大脑组织和细胞损伤,紧接着是继发性损伤后遗症,具有延迟性和持续性损伤。这种继发性损伤包括可能导致慢性神经变性和永久性功能和认知缺陷的病理过程。TBI还与发生神经退行性疾病的风险增加有关,如阿尔茨海默病(AD)、额颞叶痴呆(FTD)和肌萎缩侧索硬化症(ALS)的共同病理特征。例如,TAR dna结合蛋白43 (TDP-43)的异常,包括细胞质错误定位、胞质聚集、磷酸化和泛素化的增加,在高达50%的FTD病例和高达70%的AD病例中都可以看到,并且在> 97%的病例中被认为是ALS的标志性病理。然而,TDP-43病理在tbi后的患病率尚未得到充分表征。本研究采用非转基因小鼠脑外伤皮质损伤模型,在原发损伤部位远端脑组织和脊髓组织中观察了损伤诱导的标志TDP-43病变,而原发皮质损伤部位内的局灶性损伤组织不包括在内。分析显示,在损伤后180天,前脑皮层吻侧和远离原发损伤部位的神经元TDP-43错误定位的时间依赖性和显著性增加。TDP-43的错误定位也在TBI后颈脊髓腹角的神经元中检测到。此外,还发现了皮层层依赖性的影响,随着时间的推移,从表层到深层皮层从7 DPI增加到180 DPI。最后,RNAseq分析证实,随着时间的推移,神经元中涉及的几个关键生物过程的损伤诱导的失调。总的来说,这项研究证明了单一的中度TBI事件与慢性神经退行性过程之间的联系,这种联系不仅限于原发损伤部位,而且广泛分布于整个皮层和皮质脊髓束。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Traumatic brain injury induces TDP-43 mislocalization and neurodegenerative effects in tissue distal to the primary injury site in a non-transgenic mouse.

Traumatic brain injury induces TDP-43 mislocalization and neurodegenerative effects in tissue distal to the primary injury site in a non-transgenic mouse.

Traumatic brain injury induces TDP-43 mislocalization and neurodegenerative effects in tissue distal to the primary injury site in a non-transgenic mouse.

Traumatic brain injury induces TDP-43 mislocalization and neurodegenerative effects in tissue distal to the primary injury site in a non-transgenic mouse.

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.

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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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