Silva Liana C, Futerman Anthony H, Prieto Manuel
Centro de Química-Física Molecular & Institute of Nanoscience and Nanotechnology, Instituto Superior Técnico, Lisbon, Portugal.
Biophys J. 2009 Apr 22;96(8):3210-22. doi: 10.1016/j.bpj.2008.12.3923.
Lipid rafts and ceramide (Cer)-platforms are membrane domains that play an important role in several biological processes. Cer-platforms are commonly formed in the plasma membrane by the action of sphingomyelinase (SMase) upon hydrolysis of sphingomyelin (SM) within lipid rafts. The interplay among SMase activity, initial membrane properties (i.e., phase behavior and lipid lateral organization) and lipid composition, and the amount of product (Cer) generated, and how it modulates membrane properties were studied using fluorescence methodologies in model membranes. The activity of SMase was evaluated by following the hydrolysis of radioactive SM. It was observed that 1), the enzyme activity and extent of hydrolysis are strongly dependent on membrane physical properties but not on substrate content, and are higher in raft-like mixtures, i.e., mixtures with liquid-disordered/liquid-ordered phase separation; and 2), Cer-induced alterations are also dependent on membrane composition, specifically the cholesterol (Chol) content. In the lowest-Chol range, Cer segregates together with SM into small ( approximately 8.5 nm) Cer/SM-gel domains. With increasing Chol, the ability of Cer to recruit SM and form gel domains strongly decreases. In the high-Chol range, a Chol-enriched/SM-depleted liquid-ordered phase predominates. Together, these data suggest that in biological membranes, Chol in particular and raft domains in general play an important role in modulating SMase activity and regulating membrane physical properties by restraining Cer-induced alterations.
脂筏和神经酰胺(Cer)平台是在多种生物学过程中发挥重要作用的膜结构域。Cer平台通常是由鞘磷脂酶(SMase)作用于脂筏内鞘磷脂(SM)水解后在质膜中形成的。利用荧光方法在模型膜中研究了SMase活性、初始膜性质(即相行为和脂质侧向组织)与脂质组成、生成的产物(Cer)量之间的相互作用,以及Cer如何调节膜性质。通过追踪放射性SM的水解来评估SMase的活性。观察到:1)酶活性和水解程度强烈依赖于膜的物理性质而非底物含量,并且在类脂筏混合物(即具有液相无序/液相有序相分离的混合物)中更高;2)Cer诱导的变化也依赖于膜组成,特别是胆固醇(Chol)含量。在最低Chol范围内,Cer与SM一起分离成小的(约8.5纳米)Cer/SM凝胶结构域。随着Chol含量增加,Cer募集SM并形成凝胶结构域的能力显著降低。在高Chol范围内,富含Chol/耗尽SM的液相有序相占主导。总之,这些数据表明在生物膜中,特别是Chol以及一般的脂筏结构域在调节SMase活性和通过抑制Cer诱导的变化来调节膜物理性质方面发挥着重要作用。