University of Southern California, Leonard Davis School of Gerontology, Los Angeles, USA.
University of Southern California, Molecular and Cellular Biology Department, Los Angeles, USA.
Nat Commun. 2024 Oct 7;15(1):8676. doi: 10.1038/s41467-024-52886-2.
Aging is characterized by the accumulation of proteins that display amyloid-like behavior. However, the molecular mechanisms by which these proteins arise remain unclear. Here, we demonstrate that amyloid-like proteins are produced in a variety of human cell types, including stem cells, brain organoids and fully differentiated neurons by mistakes that occur in messenger RNA molecules. Some of these mistakes generate mutant proteins already known to cause disease, while others generate proteins that have not been observed before. Moreover, we show that these mistakes increase when cells are exposed to DNA damage, a major hallmark of human aging. When taken together, these experiments suggest a mechanistic link between the normal aging process and age-related diseases.
衰老是由具有淀粉样行为的蛋白质积累所特征化的。然而,这些蛋白质产生的分子机制仍不清楚。在这里,我们证明了淀粉样蛋白是由信使 RNA 分子中的错误在各种人类细胞类型中产生的,包括干细胞、脑类器官和完全分化的神经元。这些错误中的一些产生了已经知道会导致疾病的突变蛋白,而另一些则产生了以前从未观察到的蛋白。此外,我们还表明,当细胞暴露于 DNA 损伤时,这些错误会增加,而 DNA 损伤是人类衰老的一个主要标志。这些实验表明,正常衰老过程和与年龄相关的疾病之间存在机制联系。