消失的白质

Q2 Medicine
Marjo S van der Knaap, Marianna Bugiani, Truus E M Abbink
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引用次数: 0

摘要

"消失的白质"(VWM)是一种白质营养不良症,由编码真核细胞启动因子 2B(eIF2B)亚基的基因中的常染色体隐性致病变体引起。起病和病程变化极大。从出生前到衰老期,发病时间各不相同。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衰退,此外,发热感染和轻微头部外伤等应激也会导致神经功能急剧下降。由于少突胶质细胞,特别是星形胶质细胞的功能障碍,中枢神经系统白质变性是该病的主要特征。除卵巢外,大脑以外的器官很少受到影响。eIF2B 是综合应激反应(ISR)的核心调节因子。基因变异会降低 eIF2B 的活性,从而导致 eIF2B 下游的 ISR 构成性激活。令人震惊的是,ISR 在星形胶质细胞中被特异性激活。在 VWM 小鼠模型中调节 eIF2B 的活性和 ISR 的激活会影响疾病的严重程度,从而揭示了 eIF2B 调节的通路是潜在的药物靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vanishing white matter.

"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.

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来源期刊
Handbook of clinical neurology
Handbook of clinical neurology Medicine-Neurology (clinical)
CiteScore
4.10
自引率
0.00%
发文量
302
期刊介绍: The Handbook of Clinical Neurology (HCN) was originally conceived and edited by Pierre Vinken and George Bruyn as a prestigious, multivolume reference work that would cover all the disorders encountered by clinicians and researchers engaged in neurology and allied fields. The first series of the Handbook (Volumes 1-44) was published between 1968 and 1982 and was followed by a second series (Volumes 45-78), guided by the same editors, which concluded in 2002. By that time, the Handbook had come to represent one of the largest scientific works ever published. In 2002, Professors Michael J. Aminoff, François Boller, and Dick F. Swaab took on the responsibility of supervising the third (current) series, the first volumes of which published in 2003. They have designed this series to encompass both clinical neurology and also the basic and clinical neurosciences that are its underpinning. Given the enormity and complexity of the accumulating literature, it is almost impossible to keep abreast of developments in the field, thus providing the raison d''être for the series. The series will thus appeal to clinicians and investigators alike, providing to each an added dimension. Now, more than 140 volumes after it began, the Handbook of Clinical Neurology series has an unparalleled reputation for providing the latest information on fundamental research on the operation of the nervous system in health and disease, comprehensive clinical information on neurological and related disorders, and up-to-date treatment protocols.
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