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人类免疫缺陷病毒脑炎白质中天冬氨酸酰基转移酶缺乏:轴突损伤的新机制。

Aspartoacylase deficiency in the white matter of human immunodeficiency virus encephalitis: novel mechanism in axonal damage.

作者信息

Surendran Sankar, Rajasankar Srinivasagam

机构信息

Division of GSBS, UNT Health Science Center, Fort Worth, TX 76107, USA.

出版信息

Patholog Res Int. 2011;2011:426058. doi: 10.4061/2011/426058. Epub 2011 Sep 6.

Abstract

Aspartoacylase/aminoacylase II (ASPA/ACY II) is mainly synthesized in oligodendrocytes to contribute in myelin synthesis. Although axonal damage is seen in the brain with human immunodeficiency virus encephalitis (HIVE), ASPA contribution in the pathology is not known. Immunostaining study showed that ASPA protein is reduced in the white matter of patients with HIVE compared to the control. Western blot study further confirmed ASPA deficiency in the HIVE brain compared to the control. This paper suggests that HIVE condition affects ASPA to contribute in myelin loss/axonal damage seen in the disease.

摘要

天冬氨酸酰化酶/氨基酰化酶II(ASPA/ACY II)主要在少突胶质细胞中合成,对髓鞘合成有贡献。虽然在人类免疫缺陷病毒脑炎(HIVE)患者的大脑中可见轴突损伤,但ASPA在该病理过程中的作用尚不清楚。免疫染色研究表明,与对照组相比,HIVE患者白质中的ASPA蛋白减少。蛋白质印迹研究进一步证实,与对照组相比,HIVE患者大脑中存在ASPA缺乏。本文表明,HIVE状态会影响ASPA,导致该疾病中出现的髓鞘丢失/轴突损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20ea/3170792/78291e5dc724/PRI2011-426058.001.jpg

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