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脑白质消失。

Vanishing white matter.

机构信息

Department of Child Neurology, Amsterdam Leukodystrophy Center, Emma Children's Hospital, Amsterdam University Medical Center, and Amsterdam Neuroscience, Cellular & Molecular Mechanisms, Vrije Universiteit, Amsterdam, The Netherlands.

Department of Pathology, Amsterdam Leukodystrophy Center, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

出版信息

Handb Clin Neurol. 2024;204:77-94. doi: 10.1016/B978-0-323-99209-1.00015-6.

Abstract

"Vanishing white matter" (VWM) is a leukodystrophy caused by autosomal recessive pathogenic variants in the genes encoding the subunits of eukaryotic initiation factor 2B (eIF2B). Disease onset and disease course are extremely variable. Onset varies from the antenatal period until senescence. The age of onset is predictive of disease severity. VWM is characterized by chronic neurologic deterioration and, additionally, episodes of rapid and major neurologic decline, provoked by stresses such as febrile infections and minor head trauma. The disease is dominated by degeneration of the white matter of the central nervous system due to dysfunction of oligodendrocytes and in particular astrocytes. Organs other than the brain are rarely affected, with the exception of the ovaries. The reason for the selective vulnerability of the white matter of the central nervous system and, less consistently, the ovaries is poorly understood. eIF2B is a central regulatory factor in the integrated stress response (ISR). Genetic variants decrease eIF2B activity and thereby cause constitutive activation of the ISR downstream of eIF2B. Strikingly, the ISR is specifically activated in astrocytes. Modulation of eIF2B activity and ISR activation in VWM mouse models impacts disease severity, revealing eIF2B-regulated pathways as potential druggable targets.

摘要

“脑白质消融症”(VWM)是一种由编码真核起始因子 2B(eIF2B)亚基的基因的常染色体隐性致病性变异引起的脑白质营养不良。疾病的发作和病程变化极大。发病从产前到老年期不等。发病年龄可预测疾病的严重程度。VWM 的特征是慢性神经功能恶化,此外,还会出现由发热性感染和轻微头部外伤等压力引起的快速和严重的神经功能下降发作。该疾病主要是由于少突胶质细胞和星形胶质细胞功能障碍导致中枢神经系统白质退化。除了卵巢外,其他器官很少受到影响。中枢神经系统白质以及卵巢选择性易损的原因尚不清楚。eIF2B 是整合应激反应(ISR)的核心调节因子。遗传变异会降低 eIF2B 的活性,从而导致 eIF2B 下游的 ISR 持续激活。引人注目的是,ISR 特异性地在星形胶质细胞中被激活。VWM 小鼠模型中 eIF2B 活性和 ISR 激活的调节会影响疾病的严重程度,表明 eIF2B 调节的途径可能是潜在的可治疗靶点。

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