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Lewis X 携带的神经酰胺能够诱导神经干细胞选择性凋亡。

Lewis X-Carrying Neoglycolipids Evoke Selective Apoptosis in Neural Stem Cells.

机构信息

Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-dori, Mizuho-ku, Nagoya, 467-8603, Japan.

Institute for Molecular Science and Okazaki Institute for Integrative Bioscience, National Institutes of Natural Sciences, 5-1 Higashiyama, Myodaiji, Okazaki, 444-8787, Japan.

出版信息

Neurochem Res. 2018 Jan;43(1):212-218. doi: 10.1007/s11064-017-2415-5. Epub 2017 Oct 10.

Abstract

N-glycans carrying the Lewis X trisaccharide [Galβ1-4 (Fucα1-3) GlcNAc] are expressed by neural stem cells (NSCs) exclusively before differentiation, and they actively contribute to the maintenance of stemness of these cells. To address the functional roles of the Lewis X-mediated molecular interactions in NSCs, we created a series of synthetic neoglycolipids that contained a Lewis X-carrying glycan connected to an acyl chain through an amide bond. The neoglycolipids formed aqueous micelles displaying functional Lewis X glycotopes. Surprisingly, the neoglycolipid micelles evoked selective apoptosis in undifferentiated NSCs, whereas their differentiated cells remained unaffected. The apoptotic activity depended on the structural integrity of the Lewis X glycotopes and also on the length of the acyl chain, with an optimum length of C18. We propose hypothetical functional mechanisms of the neoglycolipid, which involves selective NSC targeting with Lewis X glycan and apoptotic signaling by the intracellular release of fatty acids. This serendipitous finding may offer a new strategy for controlling neural cell fates using artificial glycoclusters.

摘要

N-糖链携带 Lewis X 三糖 [Galβ1-4 (Fucα1-3) GlcNAc] 仅在分化前由神经干细胞 (NSCs) 表达,并且它们积极促进这些细胞的干性维持。为了研究 Lewis X 介导的分子相互作用在 NSCs 中的功能作用,我们创建了一系列合成的神经节苷脂,其中包含通过酰胺键连接到酰链的携带 Lewis X 的聚糖。神经节苷脂形成显示功能性 Lewis X 糖表位的水性胶束。令人惊讶的是,神经节苷脂胶束在未分化的 NSCs 中引发选择性凋亡,而其分化细胞不受影响。凋亡活性取决于 Lewis X 糖表位的结构完整性,也取决于酰链的长度,C18 是最佳长度。我们提出了神经节苷脂的假设功能机制,涉及 Lewis X 糖的选择性 NSC 靶向和通过细胞内释放脂肪酸的凋亡信号。这一偶然发现可能为使用人工糖簇控制神经细胞命运提供新策略。

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