Ha Seung Hee, Kim Hyoung Kyu, Anh Nguyen Thi Tuyet, Kim Nari, Ko Kyung Soo, Rhee Byoung Doo, Han Jin
National Research Laboratory for Mitochondrial Signaling, Department of Physiology, Department of Health Sciences and Technology, BK21 Plus Project Team, College of Medicine, Cardiovascular and Metabolic Disease Center, Inje University, Busan 47392, Korea.
Department of Health Technology Development, Health Project Management Team, Korea Health Industry Development Institute (KHIDI), Cheongju 28159, Korea.
Korean J Physiol Pharmacol. 2017 Sep;21(5):531-546. doi: 10.4196/kjpp.2017.21.5.531. Epub 2017 Aug 22.
Activation of Toll-like receptor-4 (TLR-4) in articular chondrocytes increases the catabolic compartment and leads to matrix degradation during the development of osteoarthritis. In this study, we determined the proteomic and genomic alterations in human chondrocytes during lipopolysaccharide (LPS)-induced inflammation to elucidate the underlying mechanisms and consequences of TLR-4 activation. Human chondrocytes were cultured with LPS for 12, 24, and 36 h to induce TLR-4 activation. The TLR-4-induced inflammatory response was confirmed by real-time PCR analysis of increased interleukin-1 beta (IL-1β), interleukin-6 (IL-6), and tumor necrosis factor alpha (TNF-α) expression levels. In TLR-4-activated chondrocytes, proteomic changes were determined by two-dimensional electrophoresis and matrix-assisted laser desorption/ionization-mass spectroscopy analysis, and genomic changes were determined by microarray and gene ontology analyses. Proteomics analysis identified 26 proteins with significantly altered expression levels; these proteins were related to the cytoskeleton and oxidative stress responses. Gene ontology analysis indicated that LPS treatment altered specific functional pathways including 'chemotaxis', 'hematopoietic organ development', 'positive regulation of cell proliferation', and 'regulation of cytokine biosynthetic process'. Nine of the 26 identified proteins displayed the same increased expression patterns in both proteomics and genomics analyses. Western blot analysis confirmed the LPS-induced increases in expression levels of lamin A/C and annexins 4/5/6. In conclusion, this study identified the time-dependent genomic, proteomic, and functional pathway alterations that occur in chondrocytes during LPS-induced TLR-4 activation. These results provide valuable new insights into the underlying mechanisms that control the development and progression of osteoarthritis.
关节软骨细胞中Toll样受体4(TLR-4)的激活会增加分解代谢区室,并在骨关节炎发展过程中导致基质降解。在本研究中,我们确定了脂多糖(LPS)诱导的炎症过程中人类软骨细胞的蛋白质组和基因组改变,以阐明TLR-4激活的潜在机制和后果。将人类软骨细胞与LPS培养12、24和36小时以诱导TLR-4激活。通过对白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)表达水平增加的实时PCR分析,证实了TLR-4诱导的炎症反应。在TLR-4激活的软骨细胞中,通过二维电泳和基质辅助激光解吸/电离质谱分析确定蛋白质组变化,通过微阵列和基因本体分析确定基因组变化。蛋白质组学分析鉴定出26种表达水平有显著改变的蛋白质;这些蛋白质与细胞骨架和氧化应激反应有关。基因本体分析表明,LPS处理改变了特定的功能途径,包括“趋化性”、“造血器官发育”、“细胞增殖的正调控”和“细胞因子生物合成过程的调控”。在26种鉴定出的蛋白质中,有9种在蛋白质组学和基因组学分析中显示出相同的表达增加模式。蛋白质印迹分析证实了LPS诱导的核纤层蛋白A/C和膜联蛋白4/5/6表达水平的增加。总之,本研究确定了LPS诱导TLR-4激活过程中软骨细胞发生的时间依赖性基因组、蛋白质组和功能途径改变。这些结果为控制骨关节炎发展和进展的潜在机制提供了有价值的新见解。