Literature DB >> 12921786

Temporal regulation of chondrocyte metabolism in agarose constructs subjected to dynamic compression.

Tina T Chowdhury1, Dan L Bader, Julia C Shelton, David A Lee.   

Abstract

The temporal response of chondrocyte metabolism in agarose constructs subjected to different dynamic compression regimes was investigated. The current study explored the effects of continuous or intermittent compression using various duty cycles of dynamic compressive loading, over a 48 h culture period. For the continuous compression experiments, duty cycles ranged from 5400 to 172,800 and intermittent compression delivered a total of 86,400 cycles. Large numbers of duty cycles significantly stimulated proteoglycan synthesis with maximal levels obtained for constructs subjected to 12h of intermittent compression. The shortest duration of intermittent compression suggested that further cycles are inhibitory for cell proliferation. Nitrite release was independent of the length or type of compressive regime applied. The uncoupled nature of the metabolic response determined in this study suggests that mechanical conditioning regimes may be fine tuned to selectively stimulate key metabolic parameters of relevance to cartilage tissue engineering.

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Year:  2003        PMID: 12921786     DOI: 10.1016/s0003-9861(03)00340-0

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


  27 in total

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6.  Duty Cycle of Deformational Loading Influences the Growth of Engineered Articular Cartilage.

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7.  Biomechanical modulation of collagen fragment-induced anabolic and catabolic activities in chondrocyte/agarose constructs.

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8.  The dynamic mechanical environment of the chondrocyte: a biphasic finite element model of cell-matrix interactions under cyclic compressive loading.

Authors:  Eunjung Kim; Farshid Guilak; Mansoor A Haider
Journal:  J Biomech Eng       Date:  2008-12       Impact factor: 2.097

9.  The role of hydrogel structure and dynamic loading on chondrocyte gene expression and matrix formation.

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10.  Quantification of the temporal evolution of collagen orientation in mechanically conditioned engineered cardiovascular tissues.

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