Department of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, 266061, China.
Department of Emergency Medicine, Qingdao Haici Medical Group, Qingdao, Shandong, 266000, China.
Can J Physiol Pharmacol. 2019 Nov;97(11):1028-1034. doi: 10.1139/cjpp-2019-0142. Epub 2019 Jul 22.
Brd4 protein is an important epigenetic regulator involved in the process of inflammatory cytokine production in many diseases. However, whether and how Brd4 participates in the process of wear-particle-induced inflammation remain unclear. This study aimed to investigate the potential role of Brd4 in titanium (Ti) particle-induced inflammatory cytokine production in mouse macrophage RAW264.7 cells. Our experiment detected Brd4 expressed in both normal synovium and periprosthetic osteolysis interface membrane, but the expression increased in the interface membrane as compared with that in normal synovium. Treatment with Ti particles significantly increased TNF-α, IL-6, and IL-1β production in RAW264.7 cells, which was inhibited by JQ1 or Brd4-siRNA. Ti particles enhanced the expression of Brd4, which was abrogated by JQ1. Ti particles enhanced NF-κB p65 and IKK phosphorylation and attenuated IκBα protein expression, which were abrogated by JQ1. Co-immunoprecipitation analysis indicated that Ti particles promoted the binding of Brd4 to acetylated NF-κB p65 (lysine-310), which was also abrogated in JQ1-treated RAW264.7 cells. In conclusion, Brd4 expression increases in interface membrane and Brd4 participates in the production of pro-inflammatory cytokines induced by Ti particles via promoting the activation of NF-κB signaling and binding to acetylated NF-κB p65 (lysine-310) in mouse macrophages.
Brd4 蛋白是一种重要的表观遗传调节剂,参与许多疾病中炎症细胞因子的产生过程。然而,Brd4 是否以及如何参与磨损颗粒诱导的炎症过程尚不清楚。本研究旨在探讨 Brd4 在钛(Ti)颗粒诱导的小鼠巨噬细胞 RAW264.7 细胞炎症细胞因子产生中的潜在作用。我们的实验检测到 Brd4 在正常滑膜和假体周围骨溶解界面膜中均有表达,但在界面膜中的表达高于正常滑膜。Ti 颗粒处理显著增加了 RAW264.7 细胞中 TNF-α、IL-6 和 IL-1β 的产生,而 JQ1 或 Brd4-siRNA 则抑制了这种产生。Ti 颗粒增强了 Brd4 的表达,而 JQ1 则削弱了这种表达。Ti 颗粒增强了 NF-κB p65 和 IKK 的磷酸化,并减弱了 IκBα 蛋白的表达,而 JQ1 则削弱了这种表达。免疫共沉淀分析表明,Ti 颗粒促进了 Brd4 与乙酰化的 NF-κB p65(赖氨酸-310)的结合,而 JQ1 处理的 RAW264.7 细胞中这种结合也被削弱。总之,Brd4 在界面膜中的表达增加,并且 Brd4 通过促进 NF-κB 信号的激活以及与乙酰化的 NF-κB p65(赖氨酸-310)结合,参与了 Ti 颗粒诱导的小鼠巨噬细胞中促炎细胞因子的产生。