RADIOIMMUNOASSAY FOR HUMAN TYPE-II COLLAGEN

被引:10
|
作者
HENROTIN, Y [1 ]
BASSLEER, C [1 ]
COLLETTE, J [1 ]
NUSGENS, B [1 ]
FRANCHIMONT, P [1 ]
机构
[1] STATE UNIV LIEGE,DEPT DERMATOL,B-4000 SART,BELGIUM
来源
JOURNAL OF IMMUNOASSAY | 1990年 / 11卷 / 04期
关键词
extraction method; human articular cartilage type II collagen; radioimmunoassay;
D O I
10.1080/01971529008055050
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human articular cartilage type II collagen (h coll.II) was purified and used to develop a radioimmunoassay. The sequential saturation procedure allowed a sensitivity of 3 ng/tube. The intra and between assay coefficients of variation were less than 10 and 20% respectively in the linear part of the curve. The assay was highly specific for native human articular type II collagen. There was no cross-reactivity with other constituents of cartilage: human proteoglycans, fibronectin, laminin and hyaluronic acid did not interfere with the assay. No cross-reactivity existed with bovine collagen types I, III, IV. However, native collagens from human placenta (I, III, IV, V, VI), rat and calf skin type I collagens and bovine type II collagen produced a weak cross-reaction only at high doses. Concerning the latter, inhibition curves were not parallel. Parallelism of inhibition curves were observed for dilution of type II collagen, produced by human chondrocytes in three-dimensional culture. All of these characteristics indicate that radioimmunoassay of type II collagen is a very sensitive and specific method available for the study and quantification of type II collagen in in vitro experimental conditions. © 1990, Taylor & Francis Group, LLC. All rights reserved.
引用
收藏
页码:555 / 578
页数:24
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