Literature DB >> 16173089

Histochemical evidences on the chronological alterations of the hypertrophic zone of mandibular condylar cartilage.

Kazi Sazzad Hossain1, Norio Amizuka, Nobuyki Ikeda, Kayoko Nozawa-Inoue, Akiko Suzuki, Minqi Li, Kiichi Takeuchi, Megumi Aita, Yoshiro Kawano, Masaaki Hoshino, Kimimitsu Oda, Ritsuo Takagi, Takeyasu Maeda.   

Abstract

The hypertrophic chondrocytes lack the ability to proliferate, thus permitting matrix mineralization as well as vascular invasion from the bone in both the mandibular condyle and the epiphyseal cartilage. This study attempted to verify whether the histological appearance of the hypertrophic chondrocytes is in a steady state during postnatal development of the mouse mandibular condyle. Type X collagen immunohistochemistry apparently distinguished the fibrous layer described previously as the "articular zone," "articular layer," and "resting zone" from the hypertrophic zone. Interestingly, the ratio of the type X collagen-positive hypertrophic zone in the entire condyle seemed higher in the early stages but decreased in the later stages. Some apparently compacted cells in the hypertrophic zone showed proliferating cell nuclear antigen (PCNA) immunoreaction, indicating the potential for cell proliferation at the early stages. As the mice matured, in contrast, they further enlarged and assumed typical features of hypertrophic chondrocytes. Apoptotic cells were also discernible in the hypertrophic zone at the early but not later stages. Consistent with morphological configurations of hypertrophic chondrocytes, immunoreactions for alkaline phosphatase, osteopontin, and type I collagen were prominent at the later stage, but not the early stage. Cartilaginous matrices demonstrated scattered patches of mineralization at the early stage, but increased in their volume and connectivity at the later stage. Thus, the spatial and temporal occurrence of these immunoreactions as well as apoptosis likely reflect the prematurity of hypertrophying cells at the early stage, and imply a physiological relevance during the early development of the mandibular condyles. Copyright 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 16173089     DOI: 10.1002/jemt.20211

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  3 in total

1.  Isolation and characterization of murine mandibular condylar cartilage cell populations.

Authors:  J Chen; A Utreja; Z Kalajzic; T Sobue; D Rowe; S Wadhwa
Journal:  Cells Tissues Organs       Date:  2011-06-01       Impact factor: 2.481

2.  Differential gene expression in the perichondrium and cartilage of the neonatal mouse temporomandibular joint.

Authors:  R J Hinton; M Serrano; S So
Journal:  Orthod Craniofac Res       Date:  2009-08       Impact factor: 1.826

3.  Altered functional loading causes differential effects in the subchondral bone and condylar cartilage in the temporomandibular joint from young mice.

Authors:  J Chen; K P Sorensen; T Gupta; T Kilts; M Young; S Wadhwa
Journal:  Osteoarthritis Cartilage       Date:  2008-09-11       Impact factor: 6.576

  3 in total

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