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基于糖脂-糖脂相互作用的GM3表达细胞的细胞黏附、铺展和运动性。

Cell adhesion, spreading, and motility of GM3-expressing cells based on glycolipid-glycolipid interaction.

作者信息

Kojima N, Hakomori S

机构信息

Biomembrane Institute, Seattle, Washington 98119.

出版信息

J Biol Chem. 1991 Sep 15;266(26):17552-8.

PMID:1894638
Abstract

Cell lines expressing varying levels of ganglioside GM3 at the cell surface show different degrees of adhesion and spreading on solid phase coated with such glycosphingolipids (GSLs) as Gg3 (GalNAc beta 1----4Gal beta 1----4Glc beta 1----1Cer), LacCer (Gal beta 1----4Glc beta 1----1Cer), or Gb4 (GalNAc beta 1----3Gal alpha 1----4Gal beta 1----4Glc beta 1----1Cer) (where Cer is ceramide), which may have structures complementary to GM3, but not on solid phase coated with various other GSLs. The degree of cell adhesion and spreading on Gg3 was correlated with the degree of cell-surface GM3 expression, as defined by reactivity with anti-GM3 monoclonal antibody (mAb) DH2. Only cells with high GM3 expression adhered on solid phase coated with LacCer or Gb4. Adhesion of GM3-expressing cells on Gg3-, LacCer-, and Gb4-coated solid phase is based on interaction of GM3 with Gg3 and, to a lesser extent, with LacCer and Gb4, as demonstrated by: (i) the interaction of the GM3 liposome with solid phase coated with Gg3, LacCer, and Gb4, respectively; (ii) the abolition of cell adhesion on each GSL-coated solid phase by treatment of cells with mAb DH2 or sialidase; and (iii) the inhibition of cell adhesion by treatment of GSL-coated solid phase with mAb specific to each GSL. Sialosyllactosyl-lysyllysine conjugate was bound to Gg3 adsorbed on a C18 silica gel column in the presence of bivalent cation, suggesting that the carbohydrate moiety of GM3 is involved in GM3-Gg3 interaction. Not only the adhesion and spreading of GM3-expressing cells, but also their cell motility was greatly enhanced on Gg3-coated solid phase, as determined by Transwell assay and phagokinetic track assay on a gold sol-coated surface. Spreading and motility of GM3-expressing cells on Gg3-coated solid phase were both inhibited by treatment of cells with mAb DH2 or sialidase. These results provide evidence that not only cell adhesion, but also spreading and motility in these cell lines are controlled by complementary GSL-GSL interaction.

摘要

在细胞表面表达不同水平神经节苷脂GM3的细胞系,在涂有诸如Gg3(N-乙酰半乳糖胺β1----4半乳糖β1----4葡萄糖β1----1神经酰胺)、乳糖神经酰胺(半乳糖β1----4葡萄糖β1----1神经酰胺)或Gb4(N-乙酰半乳糖胺β1----3半乳糖α1----4半乳糖β1----4葡萄糖β1----1神经酰胺)(其中神经酰胺为神经鞘氨醇)等糖鞘脂(GSL)的固相上,表现出不同程度的黏附与铺展,这些糖鞘脂可能具有与GM3互补的结构,但在涂有其他各种GSL的固相上则不然。细胞在Gg3上的黏附与铺展程度,与细胞表面GM3的表达程度相关,细胞表面GM3的表达程度由与抗GM3单克隆抗体(mAb)DH2的反应性来定义。只有GM3高表达的细胞能黏附在涂有乳糖神经酰胺或Gb4的固相上。表达GM3的细胞在涂有Gg3、乳糖神经酰胺和Gb4的固相上的黏附,基于GM3与Gg3的相互作用,在较小程度上还基于与乳糖神经酰胺和Gb4的相互作用,这通过以下几点得以证明:(i)GM3脂质体分别与涂有Gg3、乳糖神经酰胺和Gb4的固相的相互作用;(ii)用mAb DH2或唾液酸酶处理细胞后,可消除细胞在每种GSL包被的固相上的黏附;(iii)用针对每种GSL的mAb处理GSL包被的固相,可抑制细胞黏附。在二价阳离子存在的情况下,唾液酸乳糖基赖氨酰赖氨共轭物与吸附在C18硅胶柱上的Gg3结合,这表明GM3的碳水化合物部分参与了GM3 - Gg3的相互作用。通过Transwell分析和在金溶胶包被表面上的吞噬动力学轨迹分析确定,不仅表达GM3的细胞的黏附与铺展,而且它们的细胞运动性在涂有Gg3的固相上也大大增强。用mAb DH2或唾液酸酶处理细胞,可抑制表达GM3的细胞在涂有Gg3的固相上的铺展和运动性。这些结果证明,不仅这些细胞系中的细胞黏附,而且铺展和运动性都受互补的GSL - GSL相互作用控制。

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