Sphingolipids and Brain Resident Macrophages in Neuroinflammation: An Emerging Aspect of Nervous System Pathology

被引:41
作者
Assi, Emma [1 ]
Cazzato, Denise [1 ]
De Palma, Clara [1 ]
Perrotta, Cristiana [1 ]
Clementi, Emilio [1 ,2 ]
Cervia, Davide [1 ,3 ]
机构
[1] Univ Milan, Luigi Sacco Univ Hosp, Dept Biomed & Clin Sci, Unit Clin Pharmacol,CNR,Inst Neurosci, I-20157 Milan, Italy
[2] E Medea Sci Inst, I-23842 Bosisio Parini, Italy
[3] Univ Tuscia, Dept Innovat Biol Agrofood & Forest Syst DIBAF, I-01100 Viterbo, Italy
来源
CLINICAL & DEVELOPMENTAL IMMUNOLOGY | 2013年
关键词
AMYLOID PRECURSOR PROTEIN; NITRIC-OXIDE SYNTHASE; ACID SPHINGOMYELINASE; SPHINGOSINE; 1-PHOSPHATE; INFLAMMATORY RESPONSES; GANGLIOSIDE METABOLISM; MICROGLIAL ACTIVATION; MEMBRANE TOPOLOGY; CERAMIDE; DISEASE;
D O I
10.1155/2013/309302
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Sphingolipid metabolism is deeply regulated along the differentiation and development of the central nervous system (CNS), and the expression of a peculiar spatially and temporarily regulated sphingolipid pattern is essential for the maintenance of the functional integrity of the nervous system. Microglia are resident macrophages of the CNS involved in general maintenance of neural environment. Modulations in microglia phenotypes may contribute to pathogenic forms of inflammation. Since defects in macrophage/microglia activity contribute to neurodegenerative diseases, it will be essential to systematically identify the components of the microglial cell response that contribute to disease progression. In such complex processes, the sphingolipid systems have recently emerged to play important roles, thus appearing as a key new player in CNS disorders. This review provides a rationale for harnessing the sphingolipid metabolic pathway as a potential target against neuroinflammation.
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页数:8
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