López-Montero Iván, Monroy Francisco, Vélez Marisela, Devaux Philippe F
Universidad Complutense de Madrid, Madrid, Spain.
Biochim Biophys Acta. 2010 Jul;1798(7):1348-56. doi: 10.1016/j.bbamem.2009.12.007. Epub 2009 Dec 21.
Ceramide is a sphingolipid present in eukaryotic cells that laterally segregates into solid domains in model lipid membranes. Imaging has provided a wealth of structural information useful to understand some of the physical properties of these domains. In biological membranes, ceramide is formed on one of the membrane leaflets by enzymatic cleavage of sphyngomyelin. Ceramide, with a smaller head size than its parent compound sphyngomyelin, induces an asymmetric membrane tension and segregates into highly ordered domains that have a much high shear viscosity than that of the surrounding lipids. These physical properties, together with the rapid transmembrane flip-flop of the locally produced ceramide, trigger a sequence of membrane perturbations that could explain the molecular mechanism by which ceramide mediates different cell responses. In this review we will try to establish a connection between the physical membrane transformations in model systems known to occur upon ceramide formation and some physiologically relevant process in which ceramide is known to participate.
神经酰胺是一种存在于真核细胞中的鞘脂,在模型脂质膜中横向分离形成固态结构域。成像技术提供了大量有用的结构信息,有助于理解这些结构域的一些物理性质。在生物膜中,神经酰胺通过鞘磷脂的酶促裂解在其中一个膜小叶上形成。与母体化合物鞘磷脂相比,神经酰胺的头部尺寸较小,会引起不对称的膜张力,并分离成高度有序的结构域,其剪切粘度远高于周围脂质。这些物理性质,再加上局部产生的神经酰胺的快速跨膜翻转,引发了一系列膜扰动,这可以解释神经酰胺介导不同细胞反应的分子机制。在这篇综述中,我们将尝试在已知的神经酰胺形成时模型系统中发生的物理膜转变与已知神经酰胺参与的一些生理相关过程之间建立联系。