Ohno Shigeru, Im Hee-Jeong, Knudson Cheryl B, Knudson Warren
Rush Medical College, Rush University Medical Center, Chicago, Illinois 60612, USA.
Arthritis Rheum. 2005 Mar;52(3):800-9. doi: 10.1002/art.20937.
To document the activity profile of transcription factors following chondrocyte stimulation with hyaluronan (HA) hexasaccharides (HA(6)) and to determine the expression of genes whose transcriptional activation is tightly associated with the transcription factors.
Nuclear extracts from bovine articular chondrocytes treated with HA(6) were subjected to transcription factor protein-DNA array analysis. Electrophoretic mobility shift assay (EMSA) analyses were performed to confirm the results of protein-DNA array. The gene expressions of matrix metalloproteinase 3 (MMP-3), type II collagen, and cartilage oligomeric matrix protein (COMP) were examined by quantitative real-time reverse transcription-polymerase chain reaction (RT-PCR), and protease activity was assessed by casein zymography.
In the protein-DNA array analysis, 12 transcription factors were up-regulated and 2 transcription factors were down-regulated in the chondrocytes treated with HA(6). The transcription factors retinoic acid receptor (RAR), retinoid X receptor (RXR), and Sp-1 exhibited >2-fold increased activity by HA(6) treatment, as confirmed by EMSA. RT-PCR analysis showed that the expression levels of MMP-3, type II collagen, and COMP messenger RNA, which are tightly associated with the activation of RAR, RXR, or Sp-1, were up-regulated by treatment with HA(6). Addition of high molecular mass HA after HA(6) treatment resulted in abrogation of the MMP-3 induction.
These results suggest that HA(6) increase the activity of multiple transcription factors in chondrocytes and signal the enhanced expression of key genes involved in cartilage-matrix remodeling and turnover. The data also demonstrate that high molecular mass HA has a potential to suppress the signaling activated by HA(6).
记录透明质酸(HA)六糖(HA(6))刺激软骨细胞后转录因子的活性概况,并确定其转录激活与转录因子紧密相关的基因的表达情况。
对用HA(6)处理的牛关节软骨细胞的核提取物进行转录因子蛋白质-DNA阵列分析。进行电泳迁移率变动分析(EMSA)以证实蛋白质-DNA阵列的结果。通过定量实时逆转录-聚合酶链反应(RT-PCR)检测基质金属蛋白酶3(MMP-3)、II型胶原和软骨寡聚基质蛋白(COMP)的基因表达,并通过酪蛋白酶谱法评估蛋白酶活性。
在蛋白质-DNA阵列分析中,用HA(6)处理的软骨细胞中有12种转录因子上调,2种转录因子下调。如EMSA所证实,维甲酸受体(RAR)、维甲酸X受体(RXR)和Sp-1转录因子经HA(6)处理后活性增加超过2倍。RT-PCR分析表明,与RAR、RXR或Sp-1激活紧密相关的MMP-3、II型胶原和COMP信使核糖核酸的表达水平经HA(6)处理后上调。HA(6)处理后添加高分子量HA导致MMP-3诱导作用的消除。
这些结果表明,HA(6)增加软骨细胞中多种转录因子的活性,并表明参与软骨基质重塑和周转的关键基因的表达增强。数据还表明,高分子量HA有抑制HA(6)激活的信号传导的潜力。