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ADAM 12-S cleaves IGFBP-3 and IGFBP-5 and is inhibited by TIMP-3.

Authors :
Loechel, F
Fox, J W
Murphy, G
Albrechtsen, R
Wewer, U M
Loechel, F
Fox, J W
Murphy, G
Albrechtsen, R
Wewer, U M
Source :
Loechel , F , Fox , J W , Murphy , G , Albrechtsen , R & Wewer , U M 2000 , ' ADAM 12-S cleaves IGFBP-3 and IGFBP-5 and is inhibited by TIMP-3. ' , Biochemical and Biophysical Research Communications , vol. 278 , no. 3 , pp. 511-5 .
Publication Year :
2000

Abstract

Udgivelsesdato: 2000-Nov-30<br />ADAMs are a family of multidomain proteins having proteolytic and cell adhesion activities. We have previously shown that ADAM 12-S, the secreted soluble form of human ADAM 12, is a catalytically active protease. We now describe the purification of full-length recombinant ADAM 12-S and demonstrate that it cleaves insulin-like growth factor binding protein-3 (IGFBP-3). This result supports a role for ADAM 12-S in the degradation of IGFBP-3 in the blood of pregnant women. Furthermore, we tested for proteolysis of other members of the IGF binding protein family and found that ADAM 12-S cleaves IGFBP-5 in addition to IGFBP-3, but does not cleave IGFBP-1, -2, -4, or -6. ADAM 12-S may therefore be the IGFBP-5 protease that is secreted by osteoblasts and other cells. Cleavage of both IGFBP-3 and -5 by ADAM 12-S was inhibited by TIMP-3, raising the possibility that TIMP-3 is a physiological inhibitor of ADAM 12-S.

Details

Database :
OAIster
Journal :
Loechel , F , Fox , J W , Murphy , G , Albrechtsen , R & Wewer , U M 2000 , ' ADAM 12-S cleaves IGFBP-3 and IGFBP-5 and is inhibited by TIMP-3. ' , Biochemical and Biophysical Research Communications , vol. 278 , no. 3 , pp. 511-5 .
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1322549309
Document Type :
Electronic Resource