Sun Yubo, Franklin Atiya M, Mauerhan David R, Hanley Edward N
Department of Orthopedic Surgery, Cannon Research, Carolinas Medical Center, PO Box 32861, Charlotte, NC 28232, USA.
Open Rheumatol J. 2017 May 31;11:62-74. doi: 10.2174/1874312901711010062. eCollection 2017.
Phosphocitrate (PC) inhibits osteoarthritis (OA) in Hartley guinea pigs. However, the underlying molecular mechanisms remain poorly understood.
This study sought to examine the biological effect of PC on OA chondrocytes and test the hypothesis that PC may exert its OA disease modifying effect, in part, by inhibiting the expression of genes implicated in OA disease process and stimulating the production of extracellular matrices.
OA chondrocytes were cultured in the absence or presence of PC. Total RNA was extracted and subjected to microarray analyses. The effect of PC on proliferation and chondrocyte-mediated calcification were examined in monolayer culture. The effect of PC on the production of extracellular matrices was examined in micromass culture.
PC downregulated the expression of numerous genes classified in proliferation and apoptosis while upregulating the expression of many genes classified in transforming growth factor-β (TGF-β) receptor signaling pathway and ossification. PC also downregulated the expressions of many genes classified in inflammatory response and Wnt receptor signaling pathways. Consistent with its effect on the expression of genes classified in proliferation, ossification, and skeletal development, PC inhibited the proliferation of OA chondrocytes and chondrocyte-mediated calcification while stimulating the production of extracellular matrices.
PC may exert its OA disease modifying effect, in part, through a crystal-independent mechanism or by inhibiting the expressions of many genes implicated in OA disease process, and at the same time, stimulating the expression of genes implicated in chondroprotection and production of extracellular matrices.
磷酸柠檬酸(PC)可抑制哈特利豚鼠的骨关节炎(OA)。然而,其潜在的分子机制仍知之甚少。
本研究旨在探讨PC对OA软骨细胞的生物学效应,并验证PC可能部分通过抑制与OA疾病进程相关的基因表达以及刺激细胞外基质的产生来发挥其OA疾病修饰作用这一假说。
在有无PC的情况下培养OA软骨细胞。提取总RNA并进行微阵列分析。在单层培养中检测PC对增殖和软骨细胞介导的钙化的影响。在微团培养中检测PC对细胞外基质产生的影响。
PC下调了许多归类于增殖和凋亡的基因的表达,同时上调了许多归类于转化生长因子-β(TGF-β)受体信号通路和骨化的基因的表达。PC还下调了许多归类于炎症反应和Wnt受体信号通路的基因的表达。与其对归类于增殖、骨化和骨骼发育的基因表达的影响一致,PC抑制了OA软骨细胞的增殖和软骨细胞介导的钙化,同时刺激了细胞外基质的产生。
PC可能部分通过非晶体依赖机制或通过抑制许多与OA疾病进程相关的基因的表达,同时刺激与软骨保护相关的基因的表达和细胞外基质的产生来发挥其OA疾病修饰作用。