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Proprotein convertase activation of aggrecanases in cartilage in situ

  作者 Malfait, AM; Arner, EC; Song, RH; Alston, JT; Markosyan, S; Staten, N; Yang, Z; Griggs, DW; Tortorella, MD  
  选自 期刊  Archives of Biochemistry and Biophysics ;  卷期  2008年478-1;  页码  43-51  
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[摘要]Proteolytic degradation of the major cartilage macromolecules, aggrecan and type 11 collagen, is a key pathological event in osteoarthritis (OA). ADAMTS-4 and ADAMTS-5, the primary aggrecanases capable of cartilage aggrecan cleavage, are synthesized as latent enzymes and require prodomain removal for activity. The N-termini of the mature proteases suggest that activation involves a proprotein convertase, but the specific family member responsible for aggrecanase activation in cartilage in situ has not been identified. Here we describe Purification of a proprotein convertase activity from human OA Cartilage. Through biochemical characterization and the use of siRNA, PACE4 was identified as a proprotein convertase responsible for activation of aggrecanases in osteoarthritic and cytokine-stimulated cartilage. Posttranslational activation of ADAMTS-4 and ADAMTS-5 was observed in the extracellular milieu of cartilage, resulting in aggrecan degradation. These findings Suggest that PACE4 represents a novel target for the development of OA therapeutics. (c) 2008 Elsevier Inc. All rights reserved.

 
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