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基于神经酰胺的分配和动态行为的脂筏证据。

Evidence of lipid rafts based on the partition and dynamic behavior of sphingomyelins.

机构信息

Department of Chemistry, Graduate School of Science, Kyushu University, 744 Motooka, Fukuoka 819-0395, Japan.

Center for Highly Advanced Integration of Nano and Life Sciences (G-CHAIN), Gifu University, Yanagido 1-1, Gifu 501-1193, Japan.

出版信息

Chem Phys Lipids. 2018 Sep;215:84-95. doi: 10.1016/j.chemphyslip.2018.07.002. Epub 2018 Jul 10.

Abstract

Sphingomyelin (SM)-rich membrane nano-domains, called lipid rafts, have attracted the interest of researchers due to their potential involvement in the formation of signaling platform. Although there are many studies on lipid rafts, the direct observation of lipid rafts is still challenging owing to two critical reasons. One is the lack of an appropriate fluorescent probe mimicking the native behavior of raft lipids; fluorescent labeling often alters the intrinsic disposition of raft lipids. The other is their spatio-temporal stability; the size of lipid rafts is much smaller than the optical resolution of usual microscopy and their lifetime is much shorter than image acquisition duration. These issues are hampering the visualization of lipid rafts. Our review highlights the recent advances in microscopic techniques to visualize the partition and dynamic behavior of SMs, disclosing the detailed structure of lipid rafts. Moreover, we will elucidate the importance of SM-SM interactions in the stabilization of signaling platforms as lipid rafts.

摘要

鞘磷脂 (SM) 丰富的膜纳米域,称为脂筏,由于它们可能参与信号平台的形成,引起了研究人员的兴趣。尽管有许多关于脂筏的研究,但由于两个关键原因,直接观察脂筏仍然具有挑战性。一个原因是缺乏模拟筏脂质天然行为的合适荧光探针;荧光标记通常会改变筏脂质的固有排列。另一个原因是它们的时空稳定性;脂筏的大小比通常的显微镜的光学分辨率小得多,它们的寿命比图像采集的持续时间短得多。这些问题阻碍了脂筏的可视化。我们的综述强调了最近在微观技术方面的进展,这些技术可用于可视化 SM 的分配和动态行为,揭示了脂筏的详细结构。此外,我们将阐明 SM-SM 相互作用在稳定信号平台作为脂筏中的重要性。

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