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The effect of surface immobilized NBD peptide on osteoclastogenesis of rough titanium plates in vitro and osseointegration of rough titanium implants in ovariectomized rats in vivo

机译:表面固定的NBD肽对去卵巢大鼠体内粗糙钛板的破骨细胞生成和粗糙钛植入物骨整合的影响

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Successful osseointegration in dental implants depends on balanced activation of osteoclasts and osteoblasts. Osteoporosis up-regulates osteoclast activity, so it is desirable to find effective interventions to inhibit osteoclastogenesis and enhance the osseointegration of implants under these conditions. It has been reported that the NF-κB essential modulator (NEMO)-binding domain (NBD) peptide can prevent osteoclast formation and bone resorption. In this study, we conjugated NBD peptide onto the surface of rough pure titanium (Ti) using the layer by layer technique. We analyzed the surface characteristics and determined the successful NBD integration by the presence of trivial granular structures, increased S elements and hydrophilia. Importantly, we first reported that Ti surface-conjugated NBD peptide retained its inhibitory effects on osteoclastogenesis by reducing osteoclast sealing zone formation and function. These effects were mediated by a reduction in NFATc1 expression, which in turn regulated integrin ανβ _(3) and MMP9 by targeting the P65 signaling pathway. In vivo TRAP staining suggested NBD-coating decreased osteoclast formation with less pseudopodia. Micro-CT and histomorphometric analysis demonstrated that NBD-coating enhanced pronounced osseointegration in vivo in ovariectomized rats. This study holds great promise for in vivo use of immobilized NBD peptide and offers an effective therapeutic approach to select more suitable Ti-implant surface modifications for improving implant osseointegration in osteoporotic patients.
机译:牙植入物中成功的骨整合取决于破骨细胞和成骨细胞的平衡活化。骨质疏松症会上调破骨细胞的活性,因此希望找到有效的干预措施来抑制破骨细胞生成并增强植入物在这些条件下的骨整合。据报道,NF-κB必需调节剂(NEMO)结合域(NBD)肽可以防止破骨细胞形成和骨吸收。在这项研究中,我们使用逐层技术将NBD肽缀合到粗糙的纯钛(Ti)表面上。我们分析了表面特征,并通过琐碎的颗粒结构,增加的S元素和亲水性确定了NBD的成功整合。重要的是,我们首先报道了钛表面结合的NBD肽通过减少破骨细胞密封区的形成和功能保留了其对破骨细胞的抑制作用。这些作用是由NFATc1表达的减少介导的,而NFATc1表达的减少又通过靶向P65信号通路来调节整联蛋白ανβ_(3)和MMP9。体内TRAP染色提示NBD涂层可减少破骨细胞形成,假足减少。显微CT和组织形态分析表明,NBD涂层在去卵巢大鼠体内增强了明显的骨整合。这项研究对于体内使用固定的NBD肽具有广阔的前景,并提供了一种有效的治疗方法,以选择更合适的Ti植入物表面修饰,以改善骨质疏松患者的植入物骨整合。

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