Unidad de Regeneración Neural, Unidad Funcional de Investigación de Enfermedades Crónicas (UFIEC), Instituto de Salud Carlos III (ISCIII), Majadahonda, 28220 Madrid, Spain.
Unidad de Biología Computacional, Unidad Funcional de Investigación de Enfermedades Crónicas (UFIEC), Instituto de Salud Carlos III (ISCIII), Majadahonda, 28220 Madrid, Spain.
Int J Mol Sci. 2021 Sep 2;22(17):9537. doi: 10.3390/ijms22179537.
Amyloid-β 42 peptide (Aβ (Aβ42)) is well-known for its involvement in the development of Alzheimer's disease (AD). Aβ42 accumulates and aggregates in fibers that precipitate in the form of plaques in the brain causing toxicity; however, like other forms of Aβ peptide, the role of these peptides remains unclear. Here we analyze and compare the effects of oligomeric and fibrillary Aβ42 peptide on the biology (cell death, proliferative rate, and cell fate specification) of differentiating human neural stem cells (hNS1 cell line). By using the hNS1 cells we found that, at high concentrations, oligomeric and fibrillary Aβ42 peptides provoke apoptotic cellular death and damage of DNA in these cells, but Aβ42 fibrils have the strongest effect. The data also show that both oligomeric and fibrillar Aβ42 peptides decrease cellular proliferation but Aβ42 oligomers have the greatest effect. Finally, both, oligomers and fibrils favor gliogenesis and neurogenesis in hNS1 cells, although, in this case, the effect is more prominent in oligomers. All together the findings of this study may contribute to a better understanding of the molecular mechanisms involved in the pathology of AD and to the development of human neural stem cell-based therapies for AD treatment.
淀粉样蛋白-β 42 肽(Aβ(Aβ42))是众所周知的其参与阿尔茨海默病(AD)的发展。Aβ42 在纤维中积累和聚集,以斑块的形式沉淀在大脑中,引起毒性;然而,与其他形式的 Aβ 肽一样,这些肽的作用仍不清楚。在这里,我们分析和比较寡聚体和纤维状 Aβ42 肽对分化的人神经干细胞(hNS1 细胞系)生物学(细胞死亡、增殖率和细胞命运特化)的影响。通过使用 hNS1 细胞,我们发现,在高浓度下,寡聚体和纤维状 Aβ42 肽会引起这些细胞的凋亡性细胞死亡和 DNA 损伤,但 Aβ42 纤维具有最强的作用。数据还表明,寡聚体和纤维状 Aβ42 肽都能降低细胞增殖,但 Aβ42 寡聚体的效果最大。最后,寡聚体和纤维都有利于 hNS1 细胞中的神经胶质发生和神经发生,尽管在这种情况下,寡聚体的效果更为明显。总之,这项研究的结果可能有助于更好地理解 AD 病理学中涉及的分子机制,并为 AD 治疗的人神经干细胞为基础的治疗方法的发展做出贡献。