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[鞘脂介导的凋亡信号通路]

[Sphingolipid-mediated apoptotic signaling pathways].

作者信息

Cuvillier Olivier, Andrieu-Abadie Nathalie, Ségui Bruno, Malagarie-Cazenave Sophie, Tardy Claudine, Bonhoure Elisabeth, Levade Thierry

机构信息

Laboratoire de Biochimie IV Maladies Métaboliques et INSERM Unité 466, Institut Louis Bugnard, CHU Rangueil, 31059 Toulouse, France.

出版信息

J Soc Biol. 2003;197(3):217-21.

Abstract

Various sphingolipids are being viewed as bioactive molecules and/or second messengers. Among them, ceramide (or N-acylsphingosine) and sphingosine generally behave as pro-apoptotic mediators. Indeed, ceramide mediates the death signal initiated by numerous stress agents which either stimulate its de novo synthesis or activate sphingomyelinases that release ceramide from sphingomyelin. For instance, the early generation of ceramide promoted by TNF is mediated by a neutral sphingomyelinase the activity of which is regulated by the FAN adaptor protein, thereby controlling caspase activation and the cell death programme. In addition, the activity of this neutral sphingomyelinase is negatively modulated by caveolin, a major constituent of some membrane microdomains. The enzyme sphingosine kinase also plays a crucial role in apoptosis signalling by regulating the intracellular levels of two sphingolipids having opposite effects, namely the pro-apoptotic sphingosine and the anti-apoptotic sphingosine 1-phosphate molecule. Ceramide and sphingosine metabolism therefore appears as a pivotal regulatory pathway in the determination of cell fate.

摘要

各种鞘脂被视为生物活性分子和/或第二信使。其中,神经酰胺(或N-酰基鞘氨醇)和鞘氨醇通常作为促凋亡介质。实际上,神经酰胺介导由多种应激因素引发的死亡信号,这些应激因素要么刺激其从头合成,要么激活鞘磷脂酶,从而从鞘磷脂中释放神经酰胺。例如,肿瘤坏死因子(TNF)促进的神经酰胺早期生成是由一种中性鞘磷脂酶介导的,其活性受FAN衔接蛋白调节,从而控制半胱天冬酶激活和细胞死亡程序。此外,这种中性鞘磷脂酶的活性受到小窝蛋白的负调节,小窝蛋白是一些膜微区的主要成分。鞘氨醇激酶通过调节两种具有相反作用的鞘脂的细胞内水平,即促凋亡的鞘氨醇和抗凋亡的1-磷酸鞘氨醇分子,在凋亡信号传导中也起着关键作用。因此,神经酰胺和鞘氨醇代谢似乎是决定细胞命运的关键调节途径。

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