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软骨肉瘤软骨细胞的膜相关透明质酸结合活性。

Membrane-associated hyaluronate-binding activity of chondrosarcoma chondrocytes.

作者信息

McCarthy M T, Toole B P

机构信息

Department of Anatomy and Cellular Biology, Tufts University Health Sciences Center, Boston, Massachusetts 02111.

出版信息

J Cell Physiol. 1989 Oct;141(1):191-202. doi: 10.1002/jcp.1041410127.

Abstract

The association of hyaluronate with the surface of chondrocytes was examined by several approaches using primary cultures of chondrocytes derived from the Swarm rat chondrosarcoma. In culture, chondrosarcoma chondrocytes produced large pericellular coats, which can be visualized by particle exclusion, and which can be removed by Streptomyces hyaluronidase. Exposure of chondrocytes, which had been metabolically labelled with 3H-acetate, to exogenous hyaluronate or to Streptomyces hyaluronidase resulted in the release of 36-38% of the endogenous, labelled chondroitin sulfate from the cell layer into the incubation solution. These results imply that at least 37% of the cell layer chondroitin sulfate proteoglycan is retained there by an interaction with hyaluronate. Thus membranes were prepared from cultured chondrocytes and examined for sites which bind 3H-hyaluronate. Binding was observed and found to be saturable, specific for hyaluronate, of high affinity (Kd = approximately 10(-10) M), and destroyed by treating the membranes with trypsin. The 3H-hyaluronate-binding activity was inhibited competitively by hyaluronate decasaccharides but not by hexasaccharides or octasaccharides, indicating that the binding sites recognize a sequence of hyaluronate composed of five disaccharide repeats. The binding activity was partially purified from a detergent extract of chondrocyte membranes by ion exchange chromatography on DEAE-cellulose, followed by affinity chromatography on wheat germ agglutinin-agarose. Analysis of the partially purified binding activity by SDS-PAGE revealed five protein bands of 48,000-66,000 daltons in silver-stained gels. SDS-PAGE followed by Western blotting and exposure to monoclonal antibodies which recognize epitopes present in link protein and in the hyaluronate-binding region of cartilage proteoglycan revealed no immunoreactive protein bands in the partially purified material. We conclude that one mechanism by which hyaluronate associates with the chondrocyte surface may be via interaction with a membrane-bound hyaluronate-binding protein which is distinct from link protein and proteoglycan.

摘要

采用多种方法,利用源自斯沃姆大鼠软骨肉瘤的软骨细胞原代培养物,研究了透明质酸盐与软骨细胞表面的关联。在培养过程中,软骨肉瘤软骨细胞产生了大型细胞周被膜,可通过粒子排斥法观察到,且能被链霉菌透明质酸酶去除。用³H - 乙酸盐进行代谢标记的软骨细胞,暴露于外源性透明质酸盐或链霉菌透明质酸酶后,36 - 38%的内源性、标记的硫酸软骨素从细胞层释放到培养液中。这些结果表明,至少37%的细胞层硫酸软骨素蛋白聚糖通过与透明质酸盐的相互作用而保留在那里。因此,从培养的软骨细胞制备了细胞膜,并检测了结合³H - 透明质酸盐的位点。观察到了结合现象,发现其具有饱和性、对透明质酸盐具有特异性、高亲和力(Kd约为10⁻¹⁰ M),并且用胰蛋白酶处理细胞膜后结合被破坏。³H - 透明质酸盐结合活性受到透明质酸十糖的竞争性抑制,但不受六糖或八糖的抑制,这表明结合位点识别由五个二糖重复序列组成的透明质酸序列。通过在DEAE - 纤维素上进行离子交换色谱,随后在麦胚凝集素 - 琼脂糖上进行亲和色谱,从软骨细胞膜的去污剂提取物中部分纯化了结合活性。通过SDS - PAGE对部分纯化的结合活性进行分析,在银染凝胶中显示出五条分子量为48,000 - 66,000道尔顿的蛋白带。SDS - PAGE后进行蛋白质印迹,并与识别连接蛋白和软骨蛋白聚糖透明质酸结合区域中表位的单克隆抗体反应,结果显示在部分纯化的材料中没有免疫反应性蛋白带。我们得出结论,透明质酸盐与软骨细胞表面结合的一种机制可能是通过与一种不同于连接蛋白和蛋白聚糖的膜结合透明质酸结合蛋白相互作用。

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