London Erwin
Department of Biochemistry and Cell Biology, Stony Brook University, State University of New York, Stony Brook, New York 11794-5215, USA.
J Biol Chem. 2004 Mar 12;279(11):9997-10004. doi: 10.1074/jbc.M309992200. Epub 2003 Dec 29.
Ceramide is a membrane lipid involved in a number of crucial biological processes. Recent evidence suggests that ceramide is likely to reside and function within lipid rafts; ordered sphingolipid and cholesterol-rich lipid domains believed to exist within many eukaryotic cell membranes. Using lipid vesicles containing co-existing raft domains and disordered fluid domains, we find that natural and saturated synthetic ceramides displace sterols from rafts. Other raft lipids remain raft-associated in the presence of ceramide, showing displacement is relatively specific for sterols. Like cholesterol-containing rafts, ceramide-rich "rafts" remain in a highly ordered state. Comparison of the sterol-displacing abilities of natural ceramides with those of saturated diglycerides and an unsaturated ceramide demonstrates that tight lipid packing is critical for sterol displacement by ceramide. Based on these results, and the fact that cholesterol and ceramides both have small polar headgroups, we propose that ceramides and cholesterol compete for association with rafts because of a limited capacity of raft lipids with large headgroups to accommodate small headgroup lipids in a manner that prevents unfavorable contact between the hydrocarbon groups of the small headgroup lipids and the surrounding aqueous environment. Minimizing the exposure of cholesterol and ceramide to water may be a strong driving force for the association of other molecules with rafts. Furthermore, displacement of sterol from rafts by ceramide is very likely to have marked effects upon raft structure and function, altering liquid ordered properties as well as molecular composition. In this regard, certain previously observed physiological processes may be a result of displacement. In particular, a direct connection to the previously observed sphingomyelinase-induced displacement of cholesterol from plasma membranes in cells is proposed.
神经酰胺是一种参与多种关键生物学过程的膜脂。最近的证据表明,神经酰胺可能存在于脂筏中并在其中发挥作用;脂筏是许多真核细胞膜中存在的有序鞘脂和富含胆固醇的脂质结构域。使用含有共存的筏状结构域和无序流体结构域的脂质囊泡,我们发现天然和饱和合成神经酰胺会将甾醇从脂筏中置换出来。在存在神经酰胺的情况下,其他脂筏脂质仍与脂筏相关联,表明这种置换对甾醇具有相对特异性。与含胆固醇的脂筏一样,富含神经酰胺的“脂筏”保持高度有序状态。比较天然神经酰胺与饱和甘油二酯和不饱和神经酰胺的甾醇置换能力表明,紧密的脂质堆积对于神经酰胺置换甾醇至关重要。基于这些结果,以及胆固醇和神经酰胺都具有小极性头基团这一事实,我们提出神经酰胺和胆固醇竞争与脂筏的结合,因为具有大头基团的脂筏脂质容纳小极性头基团脂质的能力有限,而这种方式可防止小极性头基团脂质的烃基与周围水环境之间产生不利接触。尽量减少胆固醇和神经酰胺与水的接触可能是其他分子与脂筏结合的强大驱动力。此外,神经酰胺将甾醇从脂筏中置换出来很可能对脂筏的结构和功能产生显著影响,改变液晶态性质以及分子组成。在这方面,某些先前观察到的生理过程可能是置换的结果。特别是,有人提出与先前观察到的鞘磷脂酶诱导胆固醇从细胞膜中置换出来存在直接联系。