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肝细胞与固定化碳水化合物的黏附。I. 糖识别之后是能量依赖的强化过程。

Hepatocyte adhesion to immobilized carbohydrates. I. Sugar recognition is followed by energy-dependent strengthening.

作者信息

Guarnaccia S P, Schnaar R L

出版信息

J Biol Chem. 1982 Dec 10;257(23):14288-92.

PMID:7142209
Abstract

Cell-cell recognition and adhesion are thought to be complex, multistep phenomena, and may involve cell surface carbohydrates and their receptors on apposing cell surfaces. We have modeled such interactions using hepatocytes and polymer (gel) surfaces derivatized with carbohydrate ligands, and have demonstrated carbohydrate-specific cell adhesion (Schnaar, R. L., Weigel, P. H., Kuhlenschmidt, M. S., Lee, Y. C., and Roseman, S. (1978) J. Biol. Chem. 253, 7940-7951). In the present studies, we have developed a method to quantitate the forces involved in cell-gel adhesion. Our method is based on that of McClay et al. (McClay, D. R., Wessel, G. M., and Marchase, R. B. (1981) Proc. Natl. Acad. Sci. U. S. A. 78, 4975-4979) which was designed to measure the forces involved in intercellular adhesion. The following results were obtained. 1) Chicken and rat hepatocytes adhere specifically to gels derivatized with N-acetylglucosamine and galactose, respectively, at either 4 degrees C or 37 degrees C. 2) At 37 degrees C, after a lag of 10-20 min, stabilization of the adhesion occurs, resulting in a 15-fold (or greater) increase in the force of adhesion. 3) This marked strengthening of adhesion does not occur at 4 degrees C and is blocked by inhibitors of oxidative phosphorylation. These data demonstrate that cells can recognize and adhere to specific carbohydrates on apposing surfaces, and can then respond by mobilizing cellular energy to strengthen that adhesion. This series of events is strikingly similar to that shown for cell-cell adhesion between hepatocytes or between neural retina cells (Umbreit, J., and Roseman, S. (1975) J. Biol. Chem. 250, 9360-9368; McClay, D. R., Wessel, G. M., and Marchase, R. B. (1981) Proc. Natl. Acad. Sci. U. S. A. 78, 4975-4979). The present results suggest that the cell surface analogs described may provide a well controlled experimental system to probe the molecular events involved in cell-cell adhesion.

摘要

细胞间的识别与黏附被认为是复杂的多步骤现象,可能涉及细胞表面碳水化合物及其在相邻细胞表面的受体。我们利用肝细胞和用碳水化合物配体衍生化的聚合物(凝胶)表面对这种相互作用进行了建模,并证明了碳水化合物特异性的细胞黏附(施纳尔,R.L.,韦格尔,P.H.,库伦施密特,M.S.,李,Y.C.,以及罗斯曼,S.(1978年)《生物化学杂志》253卷,7940 - 7951页)。在本研究中,我们开发了一种方法来定量细胞 - 凝胶黏附中涉及的力。我们的方法基于麦克雷等人的方法(麦克雷,D.R.,韦塞尔,G.M.,以及马尔查斯,R.B.(1981年)《美国国家科学院院刊》78卷,4975 - 4979页),该方法旨在测量细胞间黏附中涉及的力。获得了以下结果。1)鸡和大鼠肝细胞分别在4℃或37℃时特异性地黏附于用N - 乙酰葡糖胺和半乳糖衍生化的凝胶。2)在37℃时,经过10 - 20分钟的延迟后,黏附达到稳定,导致黏附力增加15倍(或更多)。3)这种显著的黏附增强在4℃时不发生,并且被氧化磷酸化抑制剂阻断。这些数据表明细胞能够识别并黏附于相邻表面上的特定碳水化合物,然后可以通过调动细胞能量来增强这种黏附做出反应。这一系列事件与肝细胞之间或神经视网膜细胞之间的细胞间黏附所显示的情况惊人地相似(翁布雷特,J.,以及罗斯曼,S.(1975年)《生物化学杂志》250卷,9360 - 9368页;麦克雷,D.R.,韦塞尔,G.M.,以及马尔查斯,R.B.(1981年)《美国国家科学院院刊》78卷,4975 - 4979页)。目前的结果表明所描述的细胞表面类似物可能提供一个控制良好的实验系统来探究细胞间黏附中涉及的分子事件。

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