Appleford Mark R, Oh Sunho, Cole Judith A, Protivínský Jiri, Ong Joo L
University of Tennessee Health Science Center, Memphis, TN, USA.
Biomaterials. 2007 Nov;28(32):4788-94. doi: 10.1016/j.biomaterials.2007.06.010. Epub 2007 Aug 15.
This study investigated the in vitro effect of low-intensity pulsed ultrasound (LIPUS) on human embryonic palatal mesenchyme cells (HEPM, CRL-1486, ATCC, Manassas, VA), an osteoblast precursor cell line, during early adhesion to calcium phosphate scaffolds. Hydroxyapatite (HA) and beta-tricalcium phosphate (TCP) ceramic scaffolds were produced by a template coating method. Phospho-specific antibody cell-based ELISA (PACE) technique was utilized on stress activation proteins, including the extracellular signal-regulated kinase (ERK1/2), P38, c-Jun N-terminal kinase (JNK) and the anti-apoptosis mediator protein kinase B (PKB/AKT). Cell-based ELISAs were also performed on the membrane anchoring protein vinculin and alpha6beta4 integrin. LIPUS stimulated activation of PERK 1/2, PJNK, PP38 and vinculin in traditional two-dimensional (2-D) culture. Calcium release from the scaffolds was partially involved in the activation of PERK 1/2 when cell response was compared between culture on 2-D surfaces and three-dimensional (3-D) HA and TCP scaffolds. Effects of calcium extracted media from scaffolds alone could not account for the full activation of PJNK, PP38, PAKT, vinculin and alpha6beta4 integrin. LIPUS stimulation further increased PERK activity on TCP scaffolds corresponding with an increase in both vinculin and alpha6beta4 integrin levels. It was concluded from this study that LIPUS treatment can significantly affect stress signaling mediators and adhesion proteins in osteoblast precursor cells during the early cell-attachment phase to trabecular patterned scaffolds.
本研究调查了低强度脉冲超声(LIPUS)在人胚胎腭间充质细胞(HEPM,CRL-1486,美国典型培养物保藏中心,弗吉尼亚州马纳萨斯)早期黏附于磷酸钙支架过程中对其成骨细胞前体细胞系的体外作用。采用模板涂层法制备了羟基磷灰石(HA)和β-磷酸三钙(TCP)陶瓷支架。利用基于磷酸特异性抗体细胞的酶联免疫吸附测定(PACE)技术检测应激激活蛋白,包括细胞外信号调节激酶(ERK1/2)、P38、c-Jun氨基末端激酶(JNK)以及抗凋亡介质蛋白激酶B(PKB/AKT)。还对膜锚定蛋白纽蛋白和α6β4整合素进行了基于细胞的酶联免疫吸附测定。在传统二维(2-D)培养中,LIPUS刺激了ERK 1/2、JNK、P38和纽蛋白的激活。当比较二维表面培养与三维(3-D)HA和TCP支架培养时细胞的反应时,支架中的钙释放部分参与了ERK 1/2的激活。仅支架中提取的钙培养基的作用不能完全解释JNK、P38、AKT、纽蛋白和α6β4整合素的完全激活。LIPUS刺激进一步增加了TCP支架上的ERK活性,同时纽蛋白和α6β4整合素水平也相应增加。本研究得出结论,在成骨细胞前体细胞早期黏附于小梁图案化支架阶段,LIPUS处理可显著影响应激信号介质和黏附蛋白。