Bendotti C, Prosperini E, Kurosaki M, Garattini E, Terao M
Laboratory of Neuropharmacology, Centro Catullo e Daniela Borgomainerio, Istituto di Ricerche Farmacologiche Mario Negri, Milano, Italy.
Neuroreport. 1997 Jul 7;8(9-10):2343-9. doi: 10.1097/00001756-199707070-00048.
Aldehyde oxidase (AO), a protein involved in the catabolism of catecholamines, is the product of a gene potentially responsible for one of the familial forms of the motor neuron disease, amyotrophic lateral sclerosis (ALS). Here, we report on the cloning of a partial cDNA coding for the mouse enzyme. Using this cDNA as a probe, we demonstrate that the AO transcript is expressed in the epithelial component of the choroid plexus. More importantly, in the gray matter, the mRNA is selectively localized in the large motor neurons of the nuclei of facial, motor trigemini and hypoglossus nerves and in the motor neurons of the anterior horns of the spinal cord. This localization is consistent with a possible role of AO in the pathogenesis of ALS.
醛氧化酶(AO)是一种参与儿茶酚胺分解代谢的蛋白质,它是一个基因的产物,该基因可能与运动神经元疾病肌萎缩侧索硬化症(ALS)的一种家族形式有关。在此,我们报告编码小鼠该酶的部分cDNA的克隆。用此cDNA作为探针,我们证明AO转录本在脉络丛的上皮成分中表达。更重要的是,在灰质中,mRNA选择性地定位于面神经核、三叉神经运动核和舌下神经核的大型运动神经元以及脊髓前角的运动神经元中。这种定位与AO在ALS发病机制中可能发挥的作用一致。