Literature DB >> 2466716

Calcification of in vitro developed hypertrophic cartilage.

C Tacchetti1, R Quarto, G Campanile, R Cancedda.   

Abstract

We have recently reported that dedifferentiated cells derived from stage 28-30 chick embryo tibiae, when transferred in suspension culture in the presence of ascorbic acid, develop in a tissue closely resembling hypertrophic cartilage. Ultrastructural examination of this in vitro formed cartilage showed numerous matrix vesicles associated with the extracellular matrix (C. Tacchetti, R. Quarto, L. Nitsch, D. J. Hartmann, and R. Cancedda, 1987, J. Cell Biol. 105, 999-1006). In the present article we report that the in vitro developed hypertrophic cartilage undergoes calcification. We indicate a correlation between the levels of alkaline phosphatase activity and calcium deposition at different times of development. Following the transfer of cells into suspension culture and an initial lag phase, the level of alkaline phosphatase activity rapidly increased. In most experiments the maximum of activity was reached after 5 days of culture. When alkaline phosphatase activity and 45Ca deposition were measured in the same experiment, we observed that the increase in alkaline phosphatase preceded the deposition of nonwashable calcium deposits in the cartilage.

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Year:  1989        PMID: 2466716     DOI: 10.1016/0012-1606(89)90240-6

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  8 in total

1.  Differentiation and mineralization in chick chondrocytes maintained in a high cell density culture: a model for endochondral ossification.

Authors:  C Farquharson; C C Whitehead
Journal:  In Vitro Cell Dev Biol Anim       Date:  1995-04       Impact factor: 2.416

2.  Electron microscopy of calcification during high-density suspension culture of chondrocytes.

Authors:  Y Nakagawa; K Shimizu; T Hamamoto; S Kotani; T Yamamuro
Journal:  Calcif Tissue Int       Date:  1993-08       Impact factor: 4.333

3.  Culture and differentiation of chondrocytes entrapped in alginate gels.

Authors:  M Grandolfo; P D'Andrea; S Paoletti; M Martina; G Silvestrini; E Bonucci; F Vittur
Journal:  Calcif Tissue Int       Date:  1993-01       Impact factor: 4.333

4.  A hydrogel-mineral composite scaffold for osteochondral interface tissue engineering.

Authors:  Nora T Khanarian; Jie Jiang; Leo Q Wan; Van C Mow; Helen H Lu
Journal:  Tissue Eng Part A       Date:  2011-11-08       Impact factor: 3.845

5.  Viable cells are a requirement for in vitro cartilage calcification.

Authors:  A L Boskey; S B Doty; D Stiner; I Binderman
Journal:  Calcif Tissue Int       Date:  1996-03       Impact factor: 4.333

6.  Hypertrophic chondrocytes undergo further differentiation in culture.

Authors:  F Descalzi Cancedda; C Gentili; P Manduca; R Cancedda
Journal:  J Cell Biol       Date:  1992-04       Impact factor: 10.539

7.  In vitro development of hypertrophic chondrocytes starting from selected clones of dedifferentiated cells.

Authors:  R Quarto; B Dozin; C Tacchetti; G Campanile; C Malfatto; R Cancedda
Journal:  J Cell Biol       Date:  1990-04       Impact factor: 10.539

8.  Thyroid hormone, insulin, and glucocorticoids are sufficient to support chondrocyte differentiation to hypertrophy: a serum-free analysis.

Authors:  R Quarto; G Campanile; R Cancedda; B Dozin
Journal:  J Cell Biol       Date:  1992-11       Impact factor: 10.539

  8 in total

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