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无铜蓝蛋白血症:一种伴有铁稳态受损的遗传性神经退行性疾病。

Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis.

作者信息

Harris Z L, Klomp L W, Gitlin J D

机构信息

Edward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis, USA.

出版信息

Am J Clin Nutr. 1998 May;67(5 Suppl):972S-977S. doi: 10.1093/ajcn/67.5.972S.

Abstract

Aceruloplasminemia is an autosomal recessive disorder characterized by progressive neurodegeneration of the retina and basal ganglia associated with specific inherited mutations in the ceruloplasmin gene. Clinical and pathologic studies in patients with aceruloplasminemia revealed a marked accumulation of iron in affected parenchymal tissues, a finding consistent with early work identifying ceruloplasmin as a ferroxidase and with recent findings showing an essential role for a homologous copper oxidase in iron metabolism in yeast. The presence of neurologic symptoms in aceruloplasminemia is unique among the known inherited and acquired disorders of iron metabolism; recent studies revealed an essential role for astrocyte-specific expression of ceruloplasmin in iron metabolism and neuronal survival in the central nervous system. Recognition of aceruloplasminemia provides new insights into the genetic and environmental determinants of copper metabolism and has important implications for our understanding of the role of copper in human neurodegenerative diseases.

摘要

无铜蓝蛋白血症是一种常染色体隐性疾病,其特征为视网膜和基底神经节进行性神经退行性变,与铜蓝蛋白基因的特定遗传突变相关。对无铜蓝蛋白血症患者的临床和病理研究显示,受累实质组织中铁显著蓄积,这一发现与早期将铜蓝蛋白鉴定为铁氧化酶的研究结果一致,也与近期显示酵母中同源铜氧化酶在铁代谢中起关键作用的研究结果相符。在已知的遗传性和获得性铁代谢紊乱中,无铜蓝蛋白血症患者出现神经症状是其独特之处;近期研究揭示了铜蓝蛋白在星形胶质细胞中的特异性表达在铁代谢及中枢神经系统神经元存活方面的关键作用。对无铜蓝蛋白血症的认识为铜代谢的遗传和环境决定因素提供了新见解,对我们理解铜在人类神经退行性疾病中的作用具有重要意义。

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