Sphingolipids and brain resident macrophages in neuroinflammation: an emerging aspect of nervous system pathology.

Clinical & Developmental Immunology Pub Date : 2013-01-01 Epub Date: 2013-09-02 DOI:10.1155/2013/309302
Emma Assi, Denise Cazzato, Clara De Palma, Cristiana Perrotta, Emilio Clementi, Davide Cervia
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引用次数: 0

Abstract

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.

Abstract Image

神经炎症中的磷脂和脑驻留巨噬细胞:神经系统病理学的一个新方面。
鞘脂代谢在中枢神经系统(CNS)的分化和发育过程中受到深度调控,特殊的空间和临时调控鞘脂模式的表达对维持神经系统功能的完整性至关重要。小胶质细胞是中枢神经系统的常驻巨噬细胞,参与神经环境的总体维护。小胶质细胞表型的改变可能会导致致病性炎症。由于巨噬细胞/小胶质细胞活动的缺陷会导致神经退行性疾病,因此有必要系统地确定导致疾病进展的小胶质细胞反应的组成部分。在这种复杂的过程中,鞘脂系统近来发挥了重要作用,从而成为中枢神经系统疾病的一个关键新角色。本综述为利用鞘脂代谢途径作为抗击神经炎症的潜在靶点提供了理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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