Braux Julien, Velard Frédéric, Guillaume Christine, Jourdain Marie-Laure, Gangloff Sophie C, Jallot Edouard, Nedelec Jean-Marie, Laquerrière Patrice, Laurent-Maquin Dominique
EA 4691 Biomatériaux et Inflammation en Site Osseux (BIOS), SFR CAP-Santé (FED 4231), University of Reims-Champagne-Ardenne, 1 Avenue du Maréchal Juin, 51095 Reims CEDEX, France.
UFR Odontologie, University of Reims Champagne Ardenne, 2 rue du Général Koenig, 51100 Reims, France.
Materials (Basel). 2016 Dec 5;9(12):985. doi: 10.3390/ma9120985.
To avoid morbidity and limited availability associated with autografts, synthetic calcium phosphate (CaP) ceramics were extensively developed and used as bone filling materials. Controlling their induced-inflammatory response nevertheless remained a major concern. Strontium-containing CaP ceramics were recently demonstrated for impacting cytokines' secretion pattern of human primary monocytes. The present study focuses on the ability of strontium-containing CaP to control the human primary bone cell production of two major inflammatory and pro-osteoclastogenic mediators, namely MCP-1 and Gro-α, in response to ceramics particles.
This in vitro study was performed using human primary osteoblasts in which their response to ceramics was evaluated by PCR arrays, antibody arrays were used for screening and real-time PCR and ELISA for more focused analyses.
Study of mRNA and protein expression highlights that human primary bone cells are able to produce these inflammatory mediators and reveal that the adjunction of CaP in the culture medium leads to their enhanced production. Importantly, the current work determines the down-regulating effect of strontium-substituted CaP on MCP-1 and Gro-α production.
Our findings point out a new capability of strontium to modulate human primary bone cells' communication with the immune system.
为避免与自体移植物相关的发病率和可用性受限问题,合成磷酸钙(CaP)陶瓷被广泛开发并用作骨填充材料。然而,控制其引发的炎症反应仍是一个主要问题。最近有研究表明,含锶的CaP陶瓷会影响人类原代单核细胞的细胞因子分泌模式。本研究聚焦于含锶CaP控制人类原代骨细胞产生两种主要炎症和促破骨细胞生成介质(即单核细胞趋化蛋白-1(MCP-1)和生长调节致癌基因-α(Gro-α))以应对陶瓷颗粒的能力。
本体外研究使用人类原代成骨细胞,通过PCR阵列评估其对陶瓷的反应,使用抗体阵列进行筛选,并使用实时PCR和酶联免疫吸附测定(ELISA)进行更有针对性的分析。
对mRNA和蛋白质表达的研究表明,人类原代骨细胞能够产生这些炎症介质,并揭示培养基中添加CaP会导致其产量增加。重要的是,目前的研究确定了锶取代的CaP对MCP-1和Gro-α产生的下调作用。
我们的研究结果指出了锶调节人类原代骨细胞与免疫系统通讯的新能力。