Am J Physiol Cell Physiol AJP: Endocrinology and Metabolism
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Am J Physiol Cell Physiol (August 23, 2006). doi:10.1152/ajpcell.00127.2005
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Submitted on March 17, 2005
Accepted on April 24, 2006

Chondrocyte Intracellular Calcium, Cytoskeletal Organization and Gene Expression Responses to Dynamic Osmotic Loading

Pen-hsiu Grace Chao1, Alan C West2, and Clark T. Hung1*

1 Department of Biomedical Engineering, Columbia University, New York, New York, United States
2 Department of Chemical Engineering, Columbia University, New York, New York, United States

* To whom correspondence should be addressed. E-mail: cth6{at}columbia.edu.

While chondrocytes in articular cartilage experience dynamic stimuli from joint loading activities, few studies have examined the effects of dynamic osmotic loading on their signaling and biosynthetic activities. We hypothesize that dynamic osmotic loading modulates chondrocyte signaling and gene expression differently than static osmotic loading. Using a novel microfluidic device developed in our laboratory, dynamic hypotonic loading (-200 mOsm) was applied up to 0.1 Hz and chondrocyte calcium signaling, cytoskeleton organization and gene expression responses were examined. Chondrocytes exhibited decreasing volume and calcium responses with increasing loading frequency. Phalloidin staining showed osmotic loading-induced changes to the actin cytoskeleton in chondrocytes. Real-time PCR analysis revealed a stimulatory effect of dynamic osmotic loading compared with static osmotic loading. These studies illustrate the utility of the microfluidic device in cell signaling investigations, and their potential role in helping to elucidate mechanisms that mediate chondrocyte mechanotransduction to dynamic stimuli.




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S. R. Tew, M. J. Peffers, T. R. McKay, E. T. Lowe, W. S. Khan, T. E. Hardingham, and P. D. Clegg
Hyperosmolarity regulates SOX9 mRNA posttranscriptionally in human articular chondrocytes
Am J Physiol Cell Physiol, October 1, 2009; 297(4): C898 - C906.
[Abstract] [Full Text] [PDF]




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