Plummer J, Peterson A, Messer A
Wadsworth Center for Labs and Research, New York State Department of Health, Albany, New York 12201, USA.
Mol Cell Neurosci. 1995 Dec;6(6):532-43. doi: 10.1006/mcne.1995.0005.
To examine the effects of multiple stressors on the onset and specificity of a neurodegenerative disease, we derived mnd/mnd mice expressing a neurofilament-H/lacZ transgene. The mnd mutation causes adult-onset motor dysfunction, and produces abnormal ubiquitous accumulation of autofluorescent lipopigment, with retinal degeneration and late-onset motor neuron degeneration. The neurofilament H-beta-galactosidase fusion protein causes endogenous neurofilament subunits to precipitate in perikarya, but shows neither significant neuronal degeneration nor behavioral changes until advanced age. In mnd/mnd-transgenic animals, neurological symptoms, lipopigment accumulation, and motor neuron loss were substantially accelerated. Newly vulnerable populations of neurons also degenerated, including cerebellar Purkinje cells and dorsal roots. This study exemplifies a synergistic interaction between a neuron-specific and a ubiquitous defect, leading to significant neurological consequences. It further indicates that cytoskeletal abnormalities similar to those observed in late-onset human neurodegenerative disorders can interact with other cellular defects and contribute to pathogenesis.
为了研究多种应激源对神经退行性疾病发病及特异性的影响,我们培育了表达神经丝-H/乳糖酶转基因的mnd/mnd小鼠。mnd突变导致成年期运动功能障碍,并产生自荧光脂褐素的异常普遍积累,伴有视网膜变性和迟发性运动神经元变性。神经丝H-β-半乳糖苷酶融合蛋白导致内源性神经丝亚基在胞体中沉淀,但直到老年才出现明显的神经元变性或行为变化。在mnd/mnd转基因动物中,神经症状、脂褐素积累和运动神经元丧失显著加速。新出现的易损神经元群体也发生变性,包括小脑浦肯野细胞和背根神经节。本研究例证了神经元特异性缺陷和普遍存在的缺陷之间的协同相互作用,导致了显著的神经学后果。它进一步表明,与晚发性人类神经退行性疾病中观察到的类似的细胞骨架异常可与其他细胞缺陷相互作用并促进发病机制。