Tau polarizes an aging transcriptional signature to excitatory neurons and glia

作者：Timothy Wu, Jennifer Deger, Hui Ye, Caiwei Guo, Justin Dhindsa, Brandon Pekarek, Rami Al‐Ouran, Zhandong Liu, Ismael Al‐Ramahi, Juan Botas, Joshua M. Shulman · 发表于：eLife · 年份：2023 · DOI：10.7554/elife.85251 · 被引用次数：15 · 研究领域：Neuroinflammation and Neurodegeneration Mechanisms、Neuroscience and Neuropharmacology Research、Neurogenesis and neuroplasticity mechanisms

Aging is a major risk factor for Alzheimer’s disease (AD), and cell-type vulnerability underlies its characteristic clinical manifestations. We have performed longitudinal, single-cell RNA-sequencing in Drosophila with pan-neuronal expression of human tau, which forms AD neurofibrillary tangle pathology. Whereas tau- and aging-induced gene expression strongly overlap (93%), they differ in the affected cell types. In contrast to the broad impact of aging, tau-triggered changes are strongly polarized to excitatory neurons and glia. Further, tau can either activate or suppress innate immune gene expression signatures in a cell-type-specific manner. Integration of cellular abundance and gene expression pinpoints nuclear factor kappa B signaling in neurons as a marker for cellular vulnerability. We also highlight the conservation of cell-type-specific transcriptional patterns between Drosophila and human postmortem brain tissue. Overall, our results create a resource for dissection of dynamic, age-dependent gene expression changes at cellular resolution in a genetically tractable model of tauopathy.