Department of Orthopaedic Surgery, Stanford University Medical Center, 300 Pasteur Drive, Edwards Building, R-116, Stanford, California 94305-5341, USA.
J Orthop Res. 2010 May;28(5):571-7. doi: 10.1002/jor.21035.
Polymethylmethacrylate (PMMA) particles have been shown to inhibit the differentiation of osteoprogenitor cells, but the mechanism of this inhibitory effect has not been investigated. We hypothesize that the inhibitory effects of PMMA particles involve impairment of osteoprogenitor viability and direct inhibition of transcription factors that regulate osteogenesis. We challenged MC3T3-E1 osteoprogenitors with PMMA particles and examined the effects of these materials on osteoprogenitor viability and expression of transcription factors Runx2, osterix, Dlx5, and Msx2. MC3T3-E1 cells treated with PMMA particles over a 72-h period showed a significant reduction in cell viability and proliferation as indicated by a dose- and time-dependent increase in supernatant levels of lactate dehydrogenase, an intracellular enzyme released from dead cells, a dose-dependent decrease in cell number and BrdU uptake, and the presence of large numbers of positively labeled Annexin V-stained cells. The absence of apoptotic cells on TUNEL assay indicated that cell death occurred by necrosis, not apoptosis. MC3T3-E1 cells challenged with PMMA particles during the first 6 days of differentiation in osteogenic medium showed a significant dose-dependent decrease in the RNA expression of Runx2, osterix, and Dlx5 on all days of measurement, while the RNA expression of Msx2, an antagonist of Dlx5-induced osteogenesis, remained relatively unaffected. These results indicate that PMMA particles impair osteoprogenitor viability and inhibit the expression of transcription factors that promote osteoprogenitor differentiation.
聚甲基丙烯酸甲酯 (PMMA) 颗粒已被证明会抑制成骨前体细胞的分化,但这种抑制作用的机制尚未被研究。我们假设 PMMA 颗粒的抑制作用涉及到破坏成骨前体细胞的活力,以及直接抑制调节成骨的转录因子。我们用 PMMA 颗粒挑战 MC3T3-E1 成骨前体细胞,并研究这些材料对成骨前体细胞活力和转录因子 Runx2、osterix、Dlx5 和 Msx2 表达的影响。MC3T3-E1 细胞在 72 小时内用 PMMA 颗粒处理,表现出明显的细胞活力和增殖减少,这表现为上清液中乳酸脱氢酶水平的剂量和时间依赖性增加,乳酸脱氢酶是从死亡细胞中释放的一种细胞内酶,细胞数量和 BrdU 摄取的剂量依赖性减少,以及大量阳性标记的 Annexin V 染色细胞的存在。TUNEL 检测未发现凋亡细胞表明细胞死亡是由坏死而不是凋亡引起的。MC3T3-E1 细胞在成骨培养基中分化的前 6 天受到 PMMA 颗粒的挑战,在所有测量日,Runx2、osterix 和 Dlx5 的 RNA 表达都呈现出显著的剂量依赖性下降,而 Dlx5 诱导的成骨拮抗物 Msx2 的 RNA 表达相对不受影响。这些结果表明,PMMA 颗粒会损害成骨前体细胞的活力,并抑制促进成骨前体细胞分化的转录因子的表达。