Department of Pathology, Thomas Jefferson University, 1020 Locust Street, Philadelphia, PA 19107, USA.
Department of Environmental Health Sciences, Robert Stempel College of Public Health & Social Work, The Center for Translational Sciences, Florida International University, Port St. Lucie, FL 34987, USA.
Int J Mol Sci. 2023 Nov 11;24(22):16214. doi: 10.3390/ijms242216214.
A dominant mutation in hnRNPA1 causes amyotrophic lateral sclerosis (ALS), but it is not known whether this mutation leads to motor neuron death through increased or decreased function. To elucidate the relationship between pathogenic hnRNPA1 mutation and its native function, we created novel transgenic rats that overexpressed wildtype rat hnRNPA1 exclusively in motor neurons. This targeted expression of wildtype hnRNPA1 caused severe motor neuron loss and subsequent denervation muscle atrophy in transgenic rats that recapitulated the characteristics of ALS. These findings demonstrate that the augmentation of hnRNPA1 expression suffices to trigger motor neuron degeneration and the manifestation of ALS-like phenotypes. It is reasonable to infer that an amplification of an as-yet undetermined hnRNPA1 function plays a pivotal role in the pathogenesis of familial ALS caused by pathogenic hnRNPA1 mutation.
hnRNPA1 的显性突变会导致肌萎缩侧索硬化症(ALS),但尚不清楚该突变是通过增加还是减少功能导致运动神经元死亡。为了阐明致病性 hnRNPA1 突变与其天然功能之间的关系,我们创建了新型的转基因大鼠,这些大鼠仅在运动神经元中过表达野生型大鼠 hnRNPA1。野生型 hnRNPA1 的这种靶向表达导致转基因大鼠严重的运动神经元丧失和随后的去神经肌肉萎缩,这些表现与 ALS 的特征相吻合。这些发现表明,hnRNPA1 表达的增加足以引发运动神经元变性和表现出类似 ALS 的表型。可以合理地推断,一个尚未确定的 hnRNPA1 功能的扩增在由致病性 hnRNPA1 突变引起的家族性 ALS 的发病机制中起着关键作用。