scholarly journals Pregnancy-associated Plasma Protein-A2 (PAPP-A2), a Novel Insulin-like Growth Factor-binding Protein-5 Proteinase

2001 ◽  
Vol 276 (24) ◽  
pp. 21849-21853 ◽  
Author(s):  
Michael T. Overgaard ◽  
Henning B. Boldt ◽  
Lisbeth S. Laursen ◽  
Lars Sottrup-Jensen ◽  
Cheryl A. Conover ◽  
...  
2004 ◽  
Vol 379 (1) ◽  
pp. 57-64 ◽  
Author(s):  
Arun S. SIVANANDAM ◽  
Subburaman MOHAN ◽  
Hirohito KITA ◽  
Sanjay KAPUR ◽  
Shin-Tai CHEN ◽  
...  

PAPP-A (pregnancy-associated plasma protein-A) is produced by hSFs (human skin fibroblasts) and hOBs (human osteoblasts) and enhances the mitogenic activity of IGFs (insulin-like growth factors) by degradation of IGFBP-4 (insulin-like growth factor-binding protein 4). PKC (protein kinase C) activation in these cells led to reduction in IGFBP-4 proteolysis. This study was undertaken to determine the mechanism by which activation of PKC suppresses IGFBP-4 proteolysis. Treatment of hSFs/hOBs with TPA (PMA; 100 nM) reduced IGFBP-4 proteolysis without significantly decreasing the PAPP-A level in the CM (conditioned medium). Immunodepletion of the proform of eosinophil major basic protein (proMBP), a known PAPP-A inhibitor, from CM of TPA-treated cells (TPA CM) failed to increase IGFBP-4 proteolytic activity. Transduction of hSFs with proMBP retrovirus increased the concentration of proMBP up to 30 ng/ml and led to a moderate reduction in IGFBP-4 proteolysis. In contrast, TPA treatment blocked IGFBP-4 proteolysis but failed to induce a detectable amount of proMBP in the CM. While proMBP overexpression led to the formation of a covalent proMBP–PAPP-A complex and reduced the migration of PAPP-A on SDS/PAGE, TPA treatment dose- and time-dependently increased the conversion of a ≈470 kDa PAPP-A form (PAPP-A470) to a ≈400 kDa PAPP-A form (PAPP-A400). Since unreduced PAPP-A400 co-migrated with the 400 kDa recombinant PAPP-A homodimer and since PAPP-A monomers from reduced PAPP-A470 and PAPP-A400 co-migrated on SDS/PAGE, conversion of PAPP-A470 to PAPP-A400 is unlikely to be caused by proteolytic cleavage of PAPP-A. Consistent with the data showing that the increase in the ratio of PAPP-A400/PAPP-A470 is correlated with the extent of reduction in IGFBP-4 proteolysis, partially purified PAPP-A400 exhibited a 4-fold reduction in IGFBP-4 proteolytic activity compared with PAPP-A470. These data suggest that a novel mechanism, namely conversion of PAPP-A470 to the less-active PAPP-A400, could account for the TPA-induced suppression of PAPP-A activity.


2018 ◽  
Vol 9 ◽  
Author(s):  
James Beattie ◽  
Hasanain Al-Khafaji ◽  
Pernille R. Noer ◽  
Hanaa Esa Alkharobi ◽  
Aishah Alhodhodi ◽  
...  

2018 ◽  
Vol 9 ◽  
Author(s):  
James Beattie ◽  
Hasanain Al-Khafaji ◽  
Pernille R. Noer ◽  
Hanaa Esa Alkharobi ◽  
Aishah Alhodhodi ◽  
...  

FEBS Letters ◽  
2001 ◽  
Vol 504 (1-2) ◽  
pp. 36-40 ◽  
Author(s):  
Lisbeth S. Laursen ◽  
Michael T. Overgaard ◽  
Rikke Søe ◽  
Henning B. Boldt ◽  
Lars Sottrup-Jensen ◽  
...  

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