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脂质衍生化糖胺聚糖的制备,用于探究蛋白聚糖碳水化合物部分在细胞-基质相互作用中的调节功能。

Preparation of lipid-derivatized glycosaminoglycans to probe a regulatory function of the carbohydrate moieties of proteoglycans in cell-matrix interaction.

作者信息

Sugiura N, Sakurai K, Hori Y, Karasawa K, Suzuki S, Kimata K

机构信息

Institute for Molecular Science of Medicine, Aichi Medical University, Tokyo, Japan.

出版信息

J Biol Chem. 1993 Jul 25;268(21):15779-87.

PMID:8340404
Abstract

We have shown previously that chondroitin sulfate, but not heparan sulfate/heparin, linked to either natural core proteins or serum albumin interferes with cell-to-substrate adhesion, provided that the external proteoglycans are topologically immobilized on plastic plates. In order to study the roles of glycosaminoglycan chains (GAGs) as recognition structure, a new assay system is now developed which involves the conversion of free GAGs to reactive lactone derivatives selectively modified at the reducing end. The modified GAGs can be coupled to the amino group of phosphatidylethanolamino (PE) for use as probes on either plastic plates or cell surfaces. Incubation of GAG-PE solutions in polystyrene plates results in a time- and dose-dependent increase of the density of the GAG chains noncovalently immobilized onto the plates. No immobilization is detected with any of the GAG-PE samples that have been treated with phospholipase D. A M(r) 30,000 chondroitin sulfate conjugate to PE (CS-PE), when immobilized onto a fibronectin-coated well for 2 h at an initial concentration of 0.06 microgram/100 microliters/well, inhibits the adhesion of baby hamster kidney (BHK) cells to the substratum by approximately 50%, whereas heparin-, heparan sulfate-, hyaluronic acid-, and dermatan sulfate-PE do not. The effect of CS-PE is abolished by treating the CS-PE-coated plates with chondroitinase ABC. A similar level of inhibition by CS-PE is found when the RGD-containing 120-kDa fragment of fibronectin is used in place of fibronectin. CS-PE in soluble form, once exposed to BHK cells in suspension, can be associated with the cell surfaces, thereby exerting some inhibitory effects on cell-to-substrate adhesion. On a per mol basis, however, the activity of cell-associated CS-PE is far lower than that of substrate-associated CS-PE. Together the results indicate that our GAG-PEs offer useful tools for probing regulatory function of the GAG moieties of proteoglycans and further support the hypothesis that the inhibitory regulation of cell-to-matrix adhesion by large chondroitin sulfate proteoglycans is caused by an interaction between the cell surface and the chondroitin sulfate chains topologically immobilized on extracellular matrices.

摘要

我们之前已经表明,与天然核心蛋白或血清白蛋白相连的硫酸软骨素(而非硫酸乙酰肝素/肝素)会干扰细胞与底物的黏附,前提是外部蛋白聚糖拓扑固定在塑料板上。为了研究糖胺聚糖链(GAGs)作为识别结构的作用,现在开发了一种新的检测系统,该系统涉及将游离GAGs转化为在还原端选择性修饰的活性内酯衍生物。修饰后的GAGs可与磷脂酰乙醇胺(PE)的氨基偶联,用作塑料板或细胞表面的探针。将GAG-PE溶液在聚苯乙烯板中孵育会导致非共价固定在板上的GAG链密度随时间和剂量依赖性增加。用磷脂酶D处理过的任何GAG-PE样品均未检测到固定化现象。一种分子量为30,000的硫酸软骨素与PE的偶联物(CS-PE),当以0.06微克/100微升/孔的初始浓度固定在纤连蛋白包被的孔中2小时时,可抑制幼仓鼠肾(BHK)细胞与底物的黏附约50%,而肝素、硫酸乙酰肝素、透明质酸和硫酸皮肤素-PE则无此作用。用硫酸软骨素酶ABC处理CS-PE包被的板可消除CS-PE的作用。当使用含RGD的120-kDa纤连蛋白片段代替纤连蛋白时,发现CS-PE具有类似水平的抑制作用。可溶性形式的CS-PE一旦暴露于悬浮的BHK细胞中,就可与细胞表面结合,从而对细胞与底物的黏附产生一些抑制作用。然而,以每摩尔计,细胞相关的CS-PE的活性远低于底物相关的CS-PE。这些结果共同表明,我们的GAG-PEs为探究蛋白聚糖GAG部分的调节功能提供了有用的工具,并进一步支持了以下假设:大硫酸软骨素蛋白聚糖对细胞与基质黏附的抑制调节是由细胞表面与拓扑固定在细胞外基质上的硫酸软骨素链之间的相互作用引起的。

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