Candidate mediators of chondrocyte mechanotransduction via targeted and untargeted metabolomic measurements

• Published in: Archives of biochemistry and biophysics 2014-03, Vol.545, p.116-123
• Main Authors: Jutila, Aaron A., Zignego, Donald L., Hwang, Bradley K., Hilmer, Jonathan K., Hamerly, Timothy, Minor, Cody A., Walk, Seth T., June, Ronald K.
• Format: Article
• Language: English
• Subjects: Cartilage; Cell Line; Chondrocyte; Chondrocytes - cytology; Chondrocytes - metabolism; Humans; Joint biology; Mechanotransduction; Mechanotransduction, Cellular; Metabolome; Metabolomics; Metabolomics - methods; Osteoarthritis; Stress, Mechanical
• ISSN: 0003-9861; 1096-0384
• DOI: 10.1016/j.abb.2014.01.011

•SW1353 chondrocytes were mechanically compressed in a physiologically stiff 3D environment.•Following compression, untargeted and targeted metabolomics studies were performed.•This study identified candidate mediators of cellular mechanostransduction.•This research implicates central metabolism as a mechanosensitive pathway. Chondrocyte mechanotransduction is the process by which cartilage cells transduce mechanical loads into biochemical and biological signals. Previous studies have identified several pathways by which chondrocytes transduce mechanical loads, yet a general understanding of which signals are activated and in what order remains elusive. This study was performed to identify candidate mediators of chondrocyte mechanotransduction using SW1353 chondrocytes embedded in physiologically stiff agarose. Dynamic compression was applied to cell-seeded constructs for 0–30min, followed immediately by whole-cell metabolite extraction. Metabolites were detected via LC–MS, and compounds of interest were identified via database searches. We found several metabolites which were statistically different between the experimental groups, and we report the detection of 5 molecules which are not found in metabolite databases of known compounds indicating potential novel molecules. Targeted studies to quantify the response of central energy metabolites to compression found a transient increase in the ratio of NADP+ to NADPH and a continual decrease in the ratio of GDP to GTP, suggesting a flux of energy into the TCA cycle. These data are consistent with the remodeling of cytoskeletal components by mechanically induced signaling, and add substantial new data to a complex picture of how chondrocytes transduce mechanical loads.