Accepted Preprint (first posted online 3 June 2011)

    The growth plate chondrocyte and endochondral ossification

    1. Michiko Mirams
    1. E Mackie, School of Veterinary Science, University of Melbourne, Parkville, Australia
    2. L Tatarczuch, School of Veterinary Science, University of Melbourne, Parkville, Australia
    3. M Mirams, School of Veterinary Science, University of Melbourne, Parkville, Australia
    1. Correspondence: Eleanor Mackie, Email: ejmackie{at}unimelb.edu.au

    Abstract

    Endochondral ossification is the process that results in both the replacement of the embryonic cartilaginous skeleton during organogenesis and the growth of long bones until adult height is achieved. Chondrocytes play a central role in this process, contributing to longitudinal growth through a combination of proliferation, extracellular matrix secretion and hypertrophy. Terminally differentiated hypertrophic chondrocytes then die, allowing the invasion of a mixture of cells that collectively replace the cartilage tissue with bone tissue. The behaviour of growth plate chondrocytes is tightly regulated at all stages of endochondral ossification by a complex network of interactions between circulating hormones (including growth hormone and thyroid hormone), locally produced growth factors (including Indian hedgehog, WNTs, bone morphogenetic proteins and fibroblast growth factors) and the components of the extracellular matrix secreted by the chondrocytes (including collagens, proteoglycans, thrombospondins and matrilins). In turn, chondrocytes secrete factors that regulate the behaviour of the invading bone cells, including vascular endothelial growth factor and receptor activator of NFκB ligand. This review discusses how the growth plate chondrocyte contributes to endochondral ossification, with some emphasis on recent advances.

    • Received 3 February 2011
    • Received in final form 26 May 2011
    • Accepted 3 June 2011
    • Accepted Preprint first posted online on 3 June 2011

    This Article

    1. J Endocrinol JOE-11-0048
    1. Abstract
    2. All Versions of this Article:
      1. JOE-11-0048v1
      2. 211/2/109 most recent

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