Whitney Kristen, Song Won-Min, Sharma Abhijeet, Dangoor Diana K, Farrell Kurt, Krassner Margaret M, Ressler Hadley W, Christie Thomas D, Kandoi Shrishtee, Walker Ruth H, Nirenberg Melissa J, Frucht Steven J, Riboldi Giulietta M, Zhang Bin, Pereira Ana C, Crary John F
Department of Pathology, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Acta Neuropathol. 2024 Dec 9;148(1):80. doi: 10.1007/s00401-024-02823-w.
Progressive supranuclear palsy (PSP) is a sporadic neurodegenerative tauopathy variably affecting brainstem and cortical structures, and characterized by tau inclusions in neurons and glia. The precise mechanism whereby these protein aggregates lead to cell death remains unclear. To investigate the contribution of these different cellular abnormalities to PSP pathogenesis, we performed single-nucleus RNA sequencing (snRNA-seq) and analyzed 50,708 high quality nuclei targeting the diencephalon, including the subthalamic nucleus and adjacent structures, from human post-mortem PSP brains with varying degrees of pathology compared to controls. Cell-type-specific differential expression and pathway analysis identified both common and discrete changes in numerous pathways previously implicated in PSP and other neurodegenerative disorders. This included EIF2 signaling, an adaptive pathway activated in response to diverse stressors, which was activated in multiple vulnerable cell types and validated in independent snRNA-seq and bulk RNA-seq datasets. Using immunohistochemistry, we found that activated eIF2α was positively correlated with tau pathology burden in vulnerable brain regions. Multiplex immunofluorescence localized activated eIF2α positivity to hyperphosphorylated tau (p-tau) positive neurons and ALDH1L1-positive astrocytes, supporting the increased transcriptomic EIF2 activation observed in these vulnerable cell types. In conclusion, these data provide insights into cell-type-specific pathological changes in PSP and support the hypothesis that failure of adaptive stress pathways play a mechanistic role in the pathogenesis and progression of PSP.
进行性核上性麻痹(PSP)是一种散发性神经退行性tau蛋白病,可不同程度地影响脑干和皮质结构,其特征是神经元和神经胶质细胞中存在tau蛋白包涵体。这些蛋白质聚集体导致细胞死亡的确切机制尚不清楚。为了研究这些不同的细胞异常对PSP发病机制的作用,我们进行了单核RNA测序(snRNA-seq),并分析了来自人类PSP死后大脑丘脑下部包括丘脑底核和邻近结构的50708个高质量细胞核,这些大脑的病理程度各不相同,并与对照组进行了比较。细胞类型特异性差异表达和通路分析确定了许多先前与PSP和其他神经退行性疾病相关的通路中的共同和离散变化。这包括EIF2信号通路,这是一种在应对各种应激源时被激活的适应性通路,在多种易损细胞类型中被激活,并在独立的snRNA-seq和批量RNA-seq数据集中得到验证。通过免疫组织化学,我们发现活化的eIF2α与易损脑区的tau病理负担呈正相关。多重免疫荧光将活化的eIF2α阳性定位于过度磷酸化的tau(p-tau)阳性神经元和ALDH1L1阳性星形胶质细胞,支持了在这些易损细胞类型中观察到的转录组EIF2激活增加。总之,这些数据为PSP中细胞类型特异性的病理变化提供了见解,并支持适应性应激通路的功能障碍在PSP的发病机制和进展中起机制性作用这一假说。