Medina Luciana, González-Lizárraga Florencia, Dominguez-Meijide Antonio, Ploper Diego, Parrales Valeria, Sequeira Sabrina, Cima-Omori Maria-Sol, Zweckstetter Markus, Del Bel Elaine, Michel Patrick P, Outeiro Tiago Fleming, Raisman-Vozari Rita, Chehín Rosana, Socias Sergio B
Instituto de Investigación en Medicina Molecular y Celular Aplicada (IMMCA) (UNT-CONICET-SIPROSA), Tucumán, Argentina.
Department of Experimental Neurodegeneration, Center for Biostructural Imaging of Neurodegeneration, University Medical Center Goettingen, Goettingen, Germany.
Front Aging Neurosci. 2021 Mar 22;13:635760. doi: 10.3389/fnagi.2021.635760. eCollection 2021.
Tauopathies are neurodegenerative disorders with increasing incidence and still without cure. The extensive time required for development and approval of novel therapeutics highlights the need for testing and repurposing known safe molecules. Since doxycycline impacts α-synuclein aggregation and toxicity, herein we tested its effect on tau. We found that doxycycline reduces amyloid aggregation of the 2N4R and K18 isoforms of tau protein in a dose-dependent manner. Furthermore, in a cell free system doxycycline also prevents tau seeding and in cell culture reduces toxicity of tau aggregates. Overall, our results expand the spectrum of action of doxycycline against aggregation-prone proteins, opening novel perspectives for its repurposing as a disease-modifying drug for tauopathies.
tau蛋白病是一类发病率不断上升且仍无法治愈的神经退行性疾病。新型疗法的研发和获批需要漫长的时间,这凸显了对已知安全分子进行测试和重新利用的必要性。由于强力霉素会影响α-突触核蛋白的聚集和毒性,因此我们在此测试了其对tau蛋白的作用。我们发现强力霉素以剂量依赖的方式减少tau蛋白2N4R和K18异构体的淀粉样聚集。此外,在无细胞系统中,强力霉素还可防止tau蛋白种子形成,在细胞培养中可降低tau蛋白聚集体的毒性。总体而言,我们的研究结果拓宽了强力霉素对易聚集蛋白的作用谱,为其重新用作tau蛋白病的疾病修饰药物开辟了新的前景。