Identifying the human aggrecanase

被引:39
作者
Fosang, A. J. [1 ]
Rogerson, F. M.
机构
[1] Univ Melbourne, Dept Paediat, Parkville, Vic 3052, Australia
基金
英国医学研究理事会;
关键词
Aggrecan; Aggrecanase; Cartilage; ADAMTS-4; ADAMTS-5; Messenger RNA; Proteinase activity; HUMAN OSTEOARTHRITIC CARTILAGE; HUMAN ARTICULAR CHONDROCYTES; C-TERMINAL DOMAIN; ADAMTS4; AGGRECANASE-1; GENE-EXPRESSION; IN-VITRO; PROTEOLYTIC ACTIVITIES; KERATAN SULFATE; CYSTEINE SWITCH; CELL-SURFACE;
D O I
10.1016/j.joca.2010.06.014
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
It is clear that A Disintegrin And Metalloproteinase with ThromboSpondin motif (ADAMTS)-5 is the major aggrecanase in mouse cartilage, however it is not at all clear which enzyme is the major aggrecanase in human cartilage. Identifying the human aggrecanase is difficult because multiple, independent, molecular processes determine the final level of enzyme activity. As investigators, we have good methods for measuring changes in the expression of ADAMTS mRNA, and good methods for detecting aggrecanase activity, but no methods that distinguish the source of the activity. In between gene expression and enzyme action there are many processes that can potentially enhance or inhibit the final level of activity. In this editorial we discuss how each of these processes affects ADAMTS activity and argue that measuring any one process in isolation has little value in predicting overall ADAMTS activity in vivo. Crown Copyright (C) 2010 Published by Elsevier Ltd on behalf of Osteoarthritis Research Society International. All rights reserved.
引用
收藏
页码:1109 / 1116
页数:8
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