Grassmé Heike, Becker Katrin Anne
Department of Molecular Biology, University of Duisburg-Essen, Essen, Germany.
Handb Exp Pharmacol. 2013(216):305-20. doi: 10.1007/978-3-7091-1511-4_15.
Ceramide is released from sphingomyelin primarily by the activity of acid, neutral, or alkaline sphingomyelinases or is synthesized de novo. Several bacteria, viruses, and even parasites infect mammalian cells by exploiting the acid sphingomyelinase or the neutral sphingomyelinase-ceramide system, or both. Sphingomyelinases and ceramide have been shown to be crucially involved in the internalization of pathogens, the induction of apoptosis in infected cells, the intracellular activation of signaling pathways, and the release of cytokines. The diverse functions of ceramide in infections suggest that the sphingomyelinase-ceramide system is a key player in the host response to many pathogens.
神经酰胺主要通过酸性、中性或碱性鞘磷脂酶的活性从鞘磷脂中释放出来,或者从头合成。几种细菌、病毒甚至寄生虫通过利用酸性鞘磷脂酶或中性鞘磷脂酶-神经酰胺系统,或两者兼用来感染哺乳动物细胞。鞘磷脂酶和神经酰胺已被证明在病原体的内化、感染细胞中凋亡的诱导、信号通路的细胞内激活以及细胞因子的释放中起关键作用。神经酰胺在感染中的多种功能表明,鞘磷脂酶-神经酰胺系统是宿主对许多病原体反应中的关键参与者。