Karamesinis Konstantinos, Spyropoulou Anastasia, Dalagiorgou Georgia, Katsianou Maria A, Nokhbehsaim Marjan, Memmert Svenja, Deschner James, Vastardis Heleni, Piperi Christina
Department of Biological Chemistry, Medical School, National and Kapodistrian University of Athens, 75, M. Asias Street, 11527, Athens, Greece.
Department of Orthodontics, Dental School, National and Kapodistrian University of Athens, 11527, Athens, Greece.
J Orofac Orthop. 2017 Jan;78(1):21-31. doi: 10.1007/s00056-016-0061-1. Epub 2016 Dec 1.
The present study aimed to investigate the long-term effects of hydrostatic pressure on chondrocyte differentiation, as indicated by protein levels of transcription factors SOX9 and RUNX2, on transcriptional activity of SOX9, as determined by pSOX9 levels, and on the expression of polycystin-encoding genes Pkd1 and Pkd2.
ATDC5 cells were cultured in insulin-supplemented differentiation medium (ITS) and/or exposed to 14.7 kPa of hydrostatic pressure for 12, 24, 48, and 96 h. Cell extracts were assessed for SOX9, pSOX9, and RUNX2 using western immunoblotting. The Pkd1 and Pkd2 mRNA levels were detected by real-time PCR.
Hydrostatic pressure resulted in an early drop in SOX9 and pSOX9 protein levels at 12 h followed by an increase from 24 h onwards. A reverse pattern was followed by RUNX2, which reached peak levels at 24 h of hydrostatic pressure-treated chondrocytes in ITS culture. Pkd1 and Pkd2 mRNA levels increased at 24 h of combined hydrostatic pressure and ITS treatment, with the latter remaining elevated up to 96 h.
Our data indicate that long periods of continuous hydrostatic pressure stimulate chondrocyte differentiation through a series of molecular events involving SOX9, RUNX2, and polycystins-1, 2, providing a theoretical background for functional orthopedic mechanotherapies.
本研究旨在探讨静水压对软骨细胞分化的长期影响,具体指标包括转录因子SOX9和RUNX2的蛋白水平、由pSOX9水平测定的SOX9转录活性,以及多囊蛋白编码基因Pkd1和Pkd2的表达。
将ATDC5细胞培养于添加胰岛素的分化培养基(ITS)中,和/或暴露于14.7 kPa的静水压下12、24、48和96小时。使用蛋白质免疫印迹法评估细胞提取物中的SOX9、pSOX9和RUNX2。通过实时PCR检测Pkd1和Pkd2 mRNA水平。
静水压导致SOX9和pSOX9蛋白水平在12小时时早期下降,随后从24小时起升高。RUNX2呈现相反的模式,在ITS培养基中经静水压处理的软骨细胞24小时时达到峰值水平。在静水压和ITS联合处理24小时时,Pkd1和Pkd2 mRNA水平升高,后者在96小时内一直保持升高。
我们的数据表明,长时间的持续静水压通过一系列涉及SOX9、RUNX2和多囊蛋白-1、2的分子事件刺激软骨细胞分化,为功能性骨科机械疗法提供了理论背景。