## Abstract It is generally agreed that the mechanical environment of intervertebral disc cells plays an important role in maintaining a balanced matrix metabolism. The precise mechanism by which the signals are transduced into the cells is poorly understood. Osmotic changes in the extracellular ma
Mechanical loading affects the energy metabolism of intervertebral disc cells
β Scribed by Hanan N. Fernando; Jessica Czamanski; Tai-Yi Yuan; Weiyong Gu; Abdi Salahadin; Chun-Yuh Charles Huang
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 293 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0736-0266
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β¦ Synopsis
Abstract
Research has shown that mechanical loading affects matrix biosynthesis of intervertebral disc (IVD) cells; however, the pathway(s) to this effect is currently unknown. Cellular matrix biosynthesis is an energy demanding process. The objective of this study was to investigate the effects of static and dynamic compressive loading on energy metabolism of IVD cells. Porcine annulus fibrosus (AF) and nucleus pulposus (NP) cells seeded in 2% agarose were used in this experiment. Experimental groups included 15% static compression and 0.1 and 1βHz dynamic compression at 15% strain magnitude for 4βh. ATP, lactate, glucose, and nitric oxide (NO) contents in culture media, and ATP content in cellβagarose construct were measured using biochemical assays. While the total ATP content of AF cells was promoted by static and dynamic loading, only 1βHz dynamic loading increased total ATP content of NP cells. Increases in lactate production and glucose consumption of AF cells suggest that ATP production via glycolysis is promoted by dynamic compression. ATP release and NO production of AF and NP cells were significantly increased by dynamic loading. Thus, this study clearly illustrates that static and dynamic compressive loading affect IVD cell energy production while cellular responses to mechanical loading were both cell type and compression type dependent. Β© 2011 Orthopaedic Research Society Published by Wiley Periodicals, Inc. J Orthop Res 29:1634β1641, 2011
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