Carquin Mélanie, D'Auria Ludovic, Pollet Hélène, Bongarzone Ernesto R, Tyteca Donatienne
CELL Unit, de Duve Institute & Université Catholique de Louvain, UCL B1.75.05, Avenue Hippocrate, 75, B-1200 Brussels, Belgium.
The Myelin Regeneration Group at the Dept. Anatomy & Cell Biology, College of Medicine, University of Illinois, 808 S. Wood St. MC512, Chicago, IL. 60612. USA.
Prog Lipid Res. 2016 Apr;62:1-24. doi: 10.1016/j.plipres.2015.12.004. Epub 2015 Dec 29.
The concept of transient nanometric domains known as lipid rafts has brought interest to reassess the validity of the Singer-Nicolson model of a fluid bilayer for cell membranes. However, this new view is still insufficient to explain the cellular control of surface lipid diversity or membrane deformability. During the past decades, the hypothesis that some lipids form large (submicrometric/mesoscale vs nanometric rafts) and stable (>min vs s) membrane domains has emerged, largely based on indirect methods. Morphological evidence for stable submicrometric lipid domains, well-accepted for artificial and highly specialized biological membranes, was further reported for a variety of living cells from prokaryot es to yeast and mammalian cells. However, results remained questioned based on limitations of available fluorescent tools, use of poor lipid fixatives, and imaging artifacts due to non-resolved membrane projections. In this review, we will discuss recent evidence generated using powerful and innovative approaches such as lipid-specific toxin fragments that support the existence of submicrometric domains. We will integrate documented mechanisms involved in the formation and maintenance of these domains, and provide a perspective on their relevance on membrane deformability and regulation of membrane protein distribution.
被称为脂筏的瞬态纳米域概念引发了人们重新评估辛格 - 尼科尔森细胞膜流体双层模型有效性的兴趣。然而,这种新观点仍不足以解释细胞对表面脂质多样性或膜变形性的控制。在过去几十年里,基于间接方法出现了一种假说,即某些脂质形成大的(亚微米级/中尺度而非纳米级筏)且稳定的(大于分钟而非秒)膜域。稳定的亚微米级脂质域的形态学证据,在人工和高度特化的生物膜中已被广泛接受,后来在从原核生物到酵母和哺乳动物细胞在内的各种活细胞中也有进一步报道。然而,由于现有荧光工具的局限性、劣质脂质固定剂的使用以及未解析的膜突起导致的成像伪影,这些结果仍受到质疑。在这篇综述中,我们将讨论使用强大且创新的方法(如脂质特异性毒素片段)产生的最新证据,这些证据支持亚微米级域的存在。我们将整合与这些域的形成和维持相关的已记录机制,并就它们与膜变形性和膜蛋白分布调节的相关性提供一个观点。