Program in Neuroscience, Harvard Medical School, Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.
J Neurosci. 2010 Dec 1;30(48):16102-13. doi: 10.1523/JNEUROSCI.2491-10.2010.
A subset of neurodegenerative tauopathies is characterized by abundant filamentous inclusions of hyperphosphorylated tau in both neurons and glia. Although the contribution of neuronal tau to behavioral changes and neuronal loss in neurodegenerative diseases has been studied extensively, the functional consequences of tau deposition in glial cells have been less well characterized. To investigate the role of abnormal tau accumulation and aggregation in glial cells, we created a Drosophila model of glial tauopathy by expressing human wild-type tau in adult fly glial cells. Glial expression of tau resulted in robust aggregation of phosphorylated tau into fibrillary inclusions similar to human glial tangles. Tangle formation was accompanied by shortened lifespan and age-dependent apoptotic cell death of both glia and neurons. Genetic manipulation of Janus kinase/signal transducer and activator of transcription (JAK/STAT) signaling modified toxicity of glial tau. We also identified a synergistic interaction of combined tau expression in neurons and glial cells. In summary, we present a genetically tractable model of glial fibrillary tau tangle formation and identify JAK/STAT signaling as mediating the death of both glia and neurons in this model.
一组神经退行性tau 病的特征是神经元和神经胶质中富含过度磷酸化 tau 的丝状包涵体。虽然神经元 tau 对神经退行性疾病中的行为变化和神经元丢失的贡献已经被广泛研究,但 tau 在神经胶质细胞中的沉积的功能后果还没有得到很好的描述。为了研究异常 tau 积累和聚集在神经胶质细胞中的作用,我们通过在成年果蝇神经胶质细胞中表达人类野生型 tau 建立了一个神经胶质 tau 病的果蝇模型。tau 在神经胶质中的表达导致磷酸化 tau 聚集形成纤维状包涵体,类似于人类神经胶质纤维缠结。缠结的形成伴随着寿命缩短和神经胶质和神经元的年龄依赖性凋亡细胞死亡。Janus 激酶/信号转导和转录激活因子 (JAK/STAT) 信号的遗传操作修饰了神经胶质 tau 的毒性。我们还确定了神经元和神经胶质细胞中 tau 表达的协同相互作用。总之,我们提出了一个神经胶质纤维状 tau 缠结形成的遗传上易于处理的模型,并确定 JAK/STAT 信号作为该模型中神经胶质和神经元死亡的中介。