Xu Huiyun, Liu Ruofei, Ning Dandan, Zhang Jian, Yang Ruixin, Riquelme Manuel A, Li Jingbao, Jiang Jean X, Shang Peng
Key Laboratory for Space Biosciences and Biotechnology, School of Life Sciences, Northwestern Polytechnical University, Xi'an, Shaanxi, China.
Department of Biochemistry, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
J Orthop Res. 2017 Jun;35(6):1195-1202. doi: 10.1002/jor.23224. Epub 2017 May 4.
Connexin 43 (Cx43) hemichannels and gap junctions in osteocytes are responsive to mechanical loading, which is important for bone formation and remodeling. However, the mechanism of these Cx43-forming channels in the process of mechanical unloading is still not very clear. In this study, unloading caused by weightlessness was simulated by using a random position machine (RPM). Osteocytic MLO-Y4 cells were subjected to 2 h of RPM treatment, and levels of Cx43 mRNA and total and cell surface expressed protein were determined by quantitative real-time PCR, western blotting, and biotinylation analysis. Although mRNA was elevated by RPM, total protein level of Cx43 was not altered; however, surface biotinylated Cx43 was significantly reduced. Interestingly, RPM promoted the retention of Cx43 in the Golgi apparatus detected by co-immunofluorescence with antibodies against Cx43 and 58 K Golgi marker protein. Dye uptake assay showed that hemichannels were induced open after RPM for 2 h. Consistently, prostaglandin E release was increased and this increase was completely attenuated with the treatment of a Cx43 hemichannel blocking antibody. Together, this study demonstrates increased activity of Cx43 hemichannels to RPM, and active Cx43 hemichannels with prostaglandin E release are likely to module biological function under simulated weightless conditions. © 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 35:1195-1202, 2017.
骨细胞中的连接蛋白43(Cx43)半通道和缝隙连接对机械负荷有反应,这对骨形成和重塑很重要。然而,这些由Cx43形成的通道在机械卸载过程中的机制仍不是很清楚。在本研究中,使用随机定位机(RPM)模拟失重引起的卸载。对骨细胞MLO-Y4细胞进行2小时的RPM处理,并通过定量实时PCR、蛋白质印迹和生物素化分析来测定Cx43 mRNA水平以及总蛋白和细胞表面表达蛋白的水平。虽然RPM使mRNA升高,但Cx43的总蛋白水平没有改变;然而,表面生物素化的Cx43显著减少。有趣的是,通过与抗Cx43和58K高尔基体标记蛋白的抗体进行共免疫荧光检测发现,RPM促进了Cx43在高尔基体中的保留。染料摄取试验表明,RPM处理2小时后半通道被诱导开放。一致地,前列腺素E的释放增加,并且用Cx43半通道阻断抗体处理后这种增加完全被减弱。总之,本研究表明Cx43半通道对RPM的活性增加,并且在模拟失重条件下,具有前列腺素E释放的活性Cx43半通道可能调节生物学功能。©2017骨科研究协会。由威利期刊公司出版。《矫形外科研究杂志》35:1195 - 1202,2017年。