Department of Neurology, Mizuno Memorial Rehabilitation Hospital, Nisharai, Adachi-ku, Tokyo, Japan.
Department of Geriatric Medicine, Tokyo Medical University, Nishishinjuku, Shinjuku-ku, Tokyo, Japan.
Histol Histopathol. 2020 Sep;35(9):1023-1028. doi: 10.14670/HH-18-235. Epub 2020 Jun 18.
The transactivation response DNA-binding protein of 43 kDa (TDP-43) is a nuclear protein pivotal in RNA processing. Because phosphorylated TDP43 (pTDP-43) has been identified as a component of the ubiquitin-positive and tau-negative inclusions observed in the brains of frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS) patients, it is considered to play a major role in neurodegenerative processes. We previously reported that pTDP-43 is located in macrophages of atherosclerotic lesions of human carotid and major cerebral arteries. We hence hypothesized that pTDP-43 might be localized in the macrophages of other human brain lesions. Therefore, we investigated the immunolocalization of pTDP-43 in human brains with chronic cerebral infarction. Furthermore, we investigated the colocalization of pTDP-43 and the 14-3-3 eta isoform and found that pTDP-43 was localized in many macrophages located in chronic cerebral infarctions, in 6 out of the 15 human brains analyzed. pTDP-43 colocalized with the 14-3-3 eta isoform in these lesions. This is the first demonstration of pTDP-43 immunolocalization in chronic cerebral infarctions in human brains. We believe that our findings may be useful towards further understanding the pathophysiological roles of TDP-43 in various neurological disorders.
43kDa 转激活反应 DNA 结合蛋白(TDP-43)是一种在 RNA 加工中起关键作用的核蛋白。由于磷酸化 TDP43(pTDP-43)已被鉴定为额颞叶变性(FTLD)和肌萎缩侧索硬化症(ALS)患者大脑中观察到的泛素阳性和tau 阴性包涵体的组成部分,因此被认为在神经退行性过程中起主要作用。我们之前报道过 pTDP-43 位于人类颈动脉和大脑主要动脉粥样硬化病变的巨噬细胞中。因此,我们假设 pTDP-43 可能定位于其他人类脑病变的巨噬细胞中。因此,我们研究了慢性脑梗死患者大脑中 pTDP-43 的免疫定位。此外,我们还研究了 pTDP-43 和 14-3-3eta 同工型的共定位,并发现 pTDP-43 定位于慢性脑梗死中许多巨噬细胞中,在分析的 15 个人脑中,有 6 个存在 pTDP-43。在这些病变中,pTDP-43 与 14-3-3eta 同工型共定位。这是首次在人类大脑慢性脑梗死中显示 pTDP-43 免疫定位。我们相信我们的发现可能有助于进一步了解 TDP-43 在各种神经疾病中的病理生理作用。