Cisewski S E, Zhang L, Kuo J, Wright G J, Wu Y, Kern M J, Yao H
Department of Bioengineering, Clemson University, Clemson, SC, United States.
Department of Oral Health Sciences, Medical University of South Carolina (MUSC), Charleston, SC, United States.
Osteoarthritis Cartilage. 2015 Oct;23(10):1790-6. doi: 10.1016/j.joca.2015.05.021. Epub 2015 May 29.
To determine the combined effect of oxygen level and glucose concentration on cell viability, ATP production, and matrix synthesis of temporomandibular joint (TMJ) disc cells.
TMJ disc cells were isolated from pigs aged 6-8 months and cultured in a monolayer. Cell cultures were preconditioned for 48 h with 0, 1.5, 5, or 25 mM glucose DMEM under 1%, 5%, 10%, or 21% O2 level, respectively. The cell viability was measured using the WST-1 assay. ATP production was determined using the Luciferin-Luciferase assay. Collagen and proteoglycan synthesis were determined by measuring the incorporation of [2, 3-(3)H] proline and [(35)S] sulfate into the cells, respectively.
TMJ disc cell viability significantly decreased (P < 0.0001) without glucose. With glucose present, decreased oxygen levels significantly increased viability (P < 0.0001), while a decrease in glucose concentration significantly decreased viability (P < 0.0001). With glucose present, decreasing oxygen levels significantly reduced ATP production (P < 0.0001) and matrix synthesis (P < 0.0001). A decreased glucose concentration significantly decreased collagen synthesis (P < 0.0001). The interaction between glucose and oxygen was significant in regards to cell viability (P < 0.0001), ATP production (P = 0.00015), and collagen (P = 0.0002) and proteoglycan synthesis (P < 0.0001).
Although both glucose and oxygen are important, glucose is the limiting nutrient for TMJ disc cell survival. At low oxygen levels, the production of ATP, collagen, and proteoglycan are severely inhibited. These results suggest that steeper nutrient gradients may exist in the TMJ disc and it may be vulnerable to pathological events that impede nutrient supply.
确定氧水平和葡萄糖浓度对颞下颌关节(TMJ)盘细胞活力、ATP生成及基质合成的联合影响。
从6 - 8月龄猪分离出TMJ盘细胞并进行单层培养。细胞培养物分别在1%、5%、10%或21%氧水平下用0、1.5、5或25 mM葡萄糖的DMEM预处理48小时。使用WST - 1法测量细胞活力。使用荧光素 - 荧光素酶法测定ATP生成。分别通过测量[2, 3 - (3)H]脯氨酸和[(35)S]硫酸盐掺入细胞来测定胶原蛋白和蛋白聚糖的合成。
无葡萄糖时,TMJ盘细胞活力显著降低(P < 0.0001)。存在葡萄糖时,氧水平降低显著提高细胞活力(P < 0.0001),而葡萄糖浓度降低显著降低细胞活力(P < 0.0001)。存在葡萄糖时,氧水平降低显著减少ATP生成(P < 0.0001)和基质合成(P < 0.0001)。葡萄糖浓度降低显著减少胶原蛋白合成(P < 0.0001)。葡萄糖与氧之间的相互作用在细胞活力(P < 0.0001)、ATP生成(P = 0.00015)、胶原蛋白(P = 0.0002)和蛋白聚糖合成(P < 0.0001)方面具有显著意义。
尽管葡萄糖和氧都很重要,但葡萄糖是TMJ盘细胞存活的限制性营养物质。在低氧水平下,ATP、胶原蛋白和蛋白聚糖的生成受到严重抑制。这些结果表明TMJ盘中可能存在更陡峭的营养物质梯度,并且它可能易受阻碍营养物质供应的病理事件影响。