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Connexin43 hemichannels mediate small molecule exchange between chondrocytes and matrix in biomechanically-stimulated temporomandibular joint cartilage

机译:连接蛋白43半通道介导生物力学刺激的颞下颌关节软骨中软骨细胞与基质之间的小分子交换。

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Objective: Connexin (Cx) 43 hemichannels play a role in mechanotransduction. This study was undertaken in order to determine if Cx43 hemichannels were activated in rat temporomandibular joint (TMJ) chondrocytes under mechanical stimulation. Methods: Sprague-Dawley rats were stimulated dental-mechanically. Cx43 expression in rat TMJ cartilage was determined with immunohistochemistry and real-time PCR, and Cx43 hemichannel opening was evaluated by the extra- and intracellular levels of prostaglandin E2 (PGE2). Both primary rat chondrocytes and ATDC5 cells were treated with fluid flow shear stress (FFSS) to induce hemichannel opening. The Cx43 expression level was then determined by real-time PCR or Western blotting, and the extent of Cx43 hemichannel opening was evaluated by measuring both PGE2 release and cellular dye uptake. Results: Cx43 expression and intra- and extracellular PGE2 levels were increased in mechanically-stimulated rat TMJ cartilage compared to the unstimulated control. The FFSS treatment increased Cx43 expression and induced Cx43 hemichannel opening in primary rat chondrocytes and ATDC5 cells indicated by enhanced PGE2 release and dye uptake. Furthermore, the Cx43 hemichannel opening could be blocked by the addition of 18β-glycyrrhetinic acid, a Cx channel inhibitor, Cx43-targeting siRNA, or by withdrawal of FFSS stimulation. The migration of cytosolic Cx43 protein to the plasma membrane in ATDC5 cells was still significant after 8h post 2-h FFSS treatment, and the Cx43 protein level was still high at 48h, which returned to control levels at 72h after treatment. Conclusion: Cx43 hemichannels are activated and mediate small molecule exchange between TMJ chondrocytes and matrix under mechanical stimulation.
机译:目的:连接蛋白(Cx)43个半通道在机械转导中起作用。进行这项研究以确定在机械刺激下大鼠颞下颌关节(TMJ)软骨细胞中是否激活了Cx43半通道。方法:对Sprague-Dawley大鼠进行牙齿机械刺激。通过免疫组织化学和实时PCR测定大鼠TMJ软骨中的Cx43表达,并通过前列腺素E2(PGE2)的细胞外和细胞内水平评估Cx43半通道的开放。大鼠原代软骨细胞和ATDC5细胞均经过流体剪切应力(FFSS)处理,以诱导半通道开放。然后通过实时PCR或Western印迹法确定Cx43的表达水平,并通过测量PGE2释放和细胞染料摄取来评估Cx43半通道的开放程度。结果:与未刺激的对照组相比,在机械刺激的大鼠TMJ软骨中Cx43表达以及细胞内和细胞外PGE2水平均升高。 FFSS处理增加了原代大鼠软骨细胞和ATDC5细胞中Cx43的表达并诱导了Cx43的半通道开放,增强了PGE2的释放和染料的吸收。此外,可通过添加18β-甘草次酸,Cx通道抑制剂,靶向Cx43的siRNA或通过撤消FFSS刺激来阻断Cx43的半通道开放。 FFSS处理2小时后8小时,ATDC5细胞中胞质Cx43蛋白向质膜的迁移仍然很明显,Cx43蛋白水平在48h仍很高,在处理72h后恢复到对照水平。结论:在机械刺激下,Cx43半通道被激活并介导TMJ软骨细胞与基质之间的小分子交换。

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