Schumacher B L, Hughes C E, Kuettner K E, Caterson B, Aydelotte M B
Department of Biochemistry, Rush Medical College at Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois 60612, USA.
J Orthop Res. 1999 Jan;17(1):110-20. doi: 10.1002/jor.1100170117.
We have previously described a large proteoglycan named superficial zone protein that was isolated and purified from culture medium of superficial slices of bovine articular cartilage. Monoclonal antibodies were raised against superficial zone protein and used as probes in Western blot analyses for immunohistochemical studies both to determine precisely which cells within the joint synthesize the proteoglycan and to isolate a cDNA fragment from a bovine chondrocyte lambdagt11 library that encodes part of the proteoglycan. The cDNA fragment that was obtained with use of monoclonal antibody 6-A-1 encodes the 3' end of the sequence for superficial zone protein. On Western blots, monoclonal antibody 3-A-4 recognized an epitope on native, but not reduced, superficial zone protein, whereas monoclonal antibody 6-A-1 reacted with both native and denatured antigen. The proteoglycan was immunolocalized with monoclonal antibody 3-A-4 in chondrocytes predominantly within the superficial zone of fetal and adult articular cartilage and in some cells of the synovial lining. However, the proteoglycan was not detected in chondrocytes deep in articular cartilage, in nasal septal cartilage, or in synovial stromal cells. The only matrix staining positively for superficial zone protein was at the articular surface bordering the synovial cavity in adult, but not fetal, joints. Isolated chondrocytes and synovial cells showed intracellular binding of monoclonal antibody 3-A-4, and flow-cytometric analysis with the antibody gave the following percentages of immunopositive cells: 37.4, 52.5, 3.4, and 7.5 from chondrocytes from the full-thickness, superficial, and deep zones and from synovial cells, respectively. Thus, both chondrocytes and synovial cells bordering the joint cavity synthesize superficial zone protein and substantiate its usefulness as a phenotypic marker of particular cellular species lining the articular cavity.
我们之前描述过一种名为表层区蛋白的大型蛋白聚糖,它是从牛关节软骨表层切片的培养基中分离纯化得到的。制备了针对表层区蛋白的单克隆抗体,并将其用作蛋白质印迹分析中的探针,用于免疫组织化学研究,以精确确定关节内哪些细胞合成该蛋白聚糖,并从牛软骨细胞λgt11文库中分离出一个编码该蛋白聚糖部分序列的cDNA片段。使用单克隆抗体6-A-1获得的cDNA片段编码表层区蛋白序列的3'端。在蛋白质印迹中,单克隆抗体3-A-4识别天然而非还原型表层区蛋白上的一个表位,而单克隆抗体6-A-1与天然和变性抗原均发生反应。用单克隆抗体3-A-4对该蛋白聚糖进行免疫定位,发现它主要存在于胎儿和成人关节软骨表层区的软骨细胞以及滑膜衬里的一些细胞中。然而,在关节软骨深层的软骨细胞、鼻中隔软骨或滑膜基质细胞中未检测到该蛋白聚糖。唯一对表层区蛋白呈阳性染色的基质是在成年而非胎儿关节中与滑膜腔相邻的关节表面。分离的软骨细胞和滑膜细胞显示单克隆抗体3-A-4的细胞内结合,用该抗体进行流式细胞术分析得到的免疫阳性细胞百分比分别为:全层、表层和深层区软骨细胞以及滑膜细胞的免疫阳性细胞百分比分别为37.4%、52.5%、3.4%和7.5%。因此,与关节腔相邻区域的软骨细胞和滑膜细胞均合成表层区蛋白,证实了它作为关节腔特定细胞类型表型标志物的用途。