Herrmann Lydia, Wiegmann Caspar, Arsalan-Werner Annika, Hilbrich Isabel, Jäger Carsten, Flach Katharina, Suttkus Anne, Lachmann Ingolf, Arendt Thomas, Holzer Max
Paul Flechsig Institute of Brain Research, Department of Molecular and Cellular Mechanism of Neurodegeneration, University of Leipzig, Leipzig, Germany.
AJ Roboscreen GmbH, Leipzig, Germany.
PLoS One. 2015 Mar 23;10(3):e0119423. doi: 10.1371/journal.pone.0119423. eCollection 2015.
Defects in intracellular transport are implicated in the pathogenesis of Alzheimer's disease (AD). Hook proteins are a family of cytoplasmic linker proteins that participate in endosomal transport. In this study we show that Hook1 and Hook3 are expressed in neurons while Hook2 is predominantly expressed in astrocytes. Furthermore, Hook proteins are associated with pathological hallmarks in AD; Hook1 and Hook3 are localized to tau aggregates and Hook2 to glial components within amyloid plaques. Additionally, the expression of Hook3 is reduced in AD. Modelling of Hook3 deficiency in cultured cells leads to slowing of endosomal transport and increases β-amyloid production. We propose that Hook3 plays a role in pathogenic events exacerbating AD.
细胞内运输缺陷与阿尔茨海默病(AD)的发病机制有关。Hook蛋白是一类参与内体运输的细胞质连接蛋白。在本研究中,我们发现Hook1和Hook3在神经元中表达,而Hook2主要在星形胶质细胞中表达。此外,Hook蛋白与AD的病理特征相关;Hook1和Hook3定位于tau聚集体,Hook2定位于淀粉样斑块内的胶质成分。此外,AD中Hook3的表达降低。在培养细胞中模拟Hook3缺陷会导致内体运输减慢并增加β-淀粉样蛋白的产生。我们认为Hook3在加剧AD的致病事件中起作用。