Literature DB >> 2447832

Metalloproteinases in endochondral bone formation: appearance of tissue inhibitor-resistant metalloproteinases.

Y Mikuni-Takagaki1, Y S Cheng.   

Abstract

Dissected embryonic chick limbs release neutral metalloproteinases during endochondral bone development. These enzymes degrade cartilage proteoglycan and gelatin in culture medium. We found the enzymes active in the medium conditioned by explants of the region adjacent to the bone marrow cavity (cavity-surround). These enzymes degrade proteoglycan (PG) and/or gelatin. These spontaneously active enzymes are resistant to serum and tissue proteinase inhibitors, alpha 2-macroglobulin, and cartilage metalloproteinase inhibitor (TIMP). The other enzymes secreted from tarsus and bone marrow explants are mostly latent in the culture medium. Activated tarsus enzymes (PG degrading and gelatinolytic) are blocked by the above inhibitors. Activated marrow enzyme does not degrade PG but is resistant to those inhibitors. Cavity-surround enzymes may play an important role in embryonic osteogenesis of long bones because of their resistance to tissue and serum inhibitors. The in vivo mechanisms by which cavity-surround enzymes are activated are yet to be determined.

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Year:  1987        PMID: 2447832     DOI: 10.1016/0003-9861(87)90524-8

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  3 in total

1.  Matrix metalloproteinase-9 in a unique proteoglycan form in avian embryonic growth plate cartilage.

Authors:  R Krishna R Patchigolla; Warren Knudson; Thomas M Schmid
Journal:  Arch Biochem Biophys       Date:  2012-02-13       Impact factor: 4.013

2.  Post-translational processing of chicken bone phosphoproteins. Identification of the bone phosphoproteins of embryonic tibia.

Authors:  Y Mikuni-Takagaki; M J Glimcher
Journal:  Biochem J       Date:  1990-06-15       Impact factor: 3.857

3.  Post-translational processing of chicken bone phosphoproteins. Identification of bone (phospho)protein kinase.

Authors:  Y Mikuni-Takagaki; M J Glimcher
Journal:  Biochem J       Date:  1990-06-15       Impact factor: 3.857

  3 in total

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