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中枢神经系统中的过氧化物酶体、髓鞘形成和轴突完整性

Peroxisomes, myelination, and axonal integrity in the CNS.

作者信息

Baes Myriam, Aubourg Patrick

机构信息

Laboratory of Cell Metabolism, KU Leuven, Leuven, Belgium.

出版信息

Neuroscientist. 2009 Aug;15(4):367-79. doi: 10.1177/1073858409336297.

Abstract

Peroxisomes are ubiquitous organelles with multiple metabolic functions, but their precise role in the maintenance of tissues is not well understood. All diseases caused by partial or complete peroxisome dysfunction are characterized by a variety of neurological abnormalities, underscoring the importance of peroxisomes in nervous tissue. The interrelationship between metabolic abnormalities, histological changes, and clinical signs in these peroxisomal diseases has not yet been clarified. During the past decade, a more systematic study of the consequences of peroxisome dysfunction was possible through the generation of knockout mice with generalized or conditional inactivation of peroxisomal proteins. It appears that peroxisomes are necessary for the preservation of axonal integrity and for the formation and maintenance of myelin.

摘要

过氧化物酶体是具有多种代谢功能的普遍存在的细胞器,但其在组织维持中的精确作用尚未得到充分理解。所有由部分或完全过氧化物酶体功能障碍引起的疾病都具有多种神经学异常特征,这突出了过氧化物酶体在神经组织中的重要性。这些过氧化物酶体疾病中代谢异常、组织学变化和临床症状之间的相互关系尚未阐明。在过去十年中,通过生成过氧化物酶体蛋白普遍或条件性失活的基因敲除小鼠,对过氧化物酶体功能障碍的后果进行了更系统的研究。过氧化物酶体似乎对于轴突完整性的维持以及髓鞘的形成和维持是必需的。

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