Literature DB >> 9005927

Aggregate degradation by growth plate proteases.

M G Ehrlich1, A L Armstrong.   

Abstract

For long bone growth to occur, calcification of the matrix must begin in the lower hypertrophic zone of the growth plate. It generally is accepted that physeal proteoglycans help regulate mineralization, and that, at least in vitro, smaller proteoglycan fragments are less inhibitory of mineral formation. It also has been shown that proteoglycan degrading enzymes are concentrated in the hypertrophic zone, where calcification occurs. Thus, one can hypothesize that these enzymes are involved in the calcification process. Proteoglycans appear mainly as the aggregate form in the physis, and this study demonstrates the ability of the naturally occurring physeal enzymes to degrade proteoglycan aggregate, without first disaggregating it. Because the matrix constituents probably limit hypertrophic cell size and shape, this degradation may have some relationship to the rate of growth of the physis.

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Year:  1997        PMID: 9005927

Source DB:  PubMed          Journal:  Clin Orthop Relat Res        ISSN: 0009-921X            Impact factor:   4.176


  2 in total

1.  Immunohistochemical and biochemical assay of MMP-3 in human dentine.

Authors:  Annalisa Mazzoni; Veronica Papa; Fernando Nato; Marcela Carrilho; Leo Tjäderhane; Alessandra Ruggeri; Pietro Gobbi; Giovanni Mazzotti; Franklin R Tay; David H Pashley; Lorenzo Breschi
Journal:  J Dent       Date:  2011-01-06       Impact factor: 4.379

2.  Gender-specific distribution of glycosaminoglycans during cartilage mineralization of human thyroid cartilage.

Authors:  Horst Claassen; Jochen Werner
Journal:  J Anat       Date:  2004-11       Impact factor: 2.610

  2 in total

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