Roughley Peter J, Mort John S
Research Unit, Shriners Hospital for Children, Montreal, QC, Canada.
Methods Mol Biol. 2012;836:219-37. doi: 10.1007/978-1-61779-498-8_15.
Aggrecan is essential for the normal function of articular cartilage and intervertebral disc, where it provides the ability for the tissues to withstand compressive loading. This property depends on both the high charge density endowed by its numerous chondroitin sulfate and keratan sulfate chains and its ability to form large molecular aggregates via interaction with hyaluronan. Degradation of aggrecan via the action of proteases takes place throughout life and the degradation products accumulate in the tissue and impair its function. Such degradation is exacerbated in degenerative or inflammatory joint disorders. The use of antibodies recognizing the various regions of aggrecan and the neoepitopes generated upon proteolytic cleavage has shown that matrix metalloproteinases and aggrecanases, members of the ADAMTS family, are responsible for aggrecan degradation, both throughout life and in disease. By using immunoblotting techniques, it is possible to determine the extent of aggrecan degradation and to identify the degradation products that have accumulated in the tissue, and immunohistochemistry allows the location of the aggrecan degradation to be established.
聚集蛋白聚糖对于关节软骨和椎间盘的正常功能至关重要,它赋予组织承受压缩负荷的能力。这种特性既取决于其众多硫酸软骨素和硫酸角质素链赋予的高电荷密度,也取决于其通过与透明质酸相互作用形成大分子聚集体的能力。在整个生命过程中,蛋白酶作用导致的聚集蛋白聚糖降解都会发生,降解产物在组织中积累并损害其功能。在退行性或炎性关节疾病中,这种降解会加剧。使用识别聚集蛋白聚糖不同区域以及蛋白水解切割产生的新表位的抗体表明,基质金属蛋白酶和ADAMTS家族成员聚集蛋白聚糖酶在整个生命过程和疾病中都负责聚集蛋白聚糖的降解。通过免疫印迹技术,可以确定聚集蛋白聚糖的降解程度,并识别在组织中积累的降解产物,免疫组织化学则可以确定聚集蛋白聚糖降解的位置。