AbdulQader Sarah Talib, Kannan Thirumulu Ponnuraj, Rahman Ismail Ab, Ismail Hanafi, Mahmood Zuliani
School of Dental Sciences, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia; Department of Pedodontic and Preventive Dentistry, College of Dentistry, University of Baghdad, Baghdad, Iraq.
School of Dental Sciences, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia; Human Genome Centre, School of Medical Sciences, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia.
Mater Sci Eng C Mater Biol Appl. 2015 Apr;49:225-233. doi: 10.1016/j.msec.2014.12.070. Epub 2014 Dec 20.
Calcium phosphate (CaP) scaffolds have been widely and successfully used with osteoblast cells for bone tissue regeneration. However, it is necessary to investigate the effects of these scaffolds on odontoblast cells' proliferation and differentiation for dentin tissue regeneration. In this study, three different hydroxyapatite (HA) to beta tricalcium phosphate (β-TCP) ratios of biphasic calcium phosphate (BCP) scaffolds, BCP20, BCP50, and BCP80, with a mean pore size of 300μm and 65% porosity were prepared from phosphoric acid (H2PO4) and calcium carbonate (CaCO3) sintered at 1000°C for 2h. The extracts of these scaffolds were assessed with regard to cell viability and differentiation of odontoblasts. The high alkalinity, more calcium, and phosphate ions released that were exhibited by BCP20 decreased the viability of human dental pulp cells (HDPCs) as compared to BCP50 and BCP80. However, the cells cultured with BCP20 extract expressed high alkaline phosphatase activity and high expression level of bone sialoprotein (BSP), dental matrix protein-1 (DMP-1), and dentin sialophosphoprotein (DSPP) genes as compared to that cultured with BCP50 and BCP80 extracts. The results highlighted the effect of different scaffold ratios on the cell microenvironment and demonstrated that BCP20 scaffold can support HDPC differentiation for dentin tissue regeneration.
磷酸钙(CaP)支架已被广泛且成功地用于与成骨细胞一起进行骨组织再生。然而,有必要研究这些支架对成牙本质细胞增殖和分化的影响,以用于牙本质组织再生。在本研究中,由磷酸(H2PO4)和碳酸钙(CaCO3)在1000°C烧结2小时制备了三种不同羟基磷灰石(HA)与β-磷酸三钙(β-TCP)比例的双相磷酸钙(BCP)支架,即BCP20、BCP50和BCP80,其平均孔径为300μm,孔隙率为65%。对这些支架的提取物进行了关于成牙本质细胞活力和分化的评估。与BCP50和BCP80相比,BCP20表现出的高碱度、更多的钙和磷酸根离子释放降低了人牙髓细胞(HDPCs)的活力。然而,与用BCP50和BCP80提取物培养的细胞相比,用BCP20提取物培养的细胞表达了高碱性磷酸酶活性以及骨涎蛋白(BSP)、牙本质基质蛋白-1(DMP-1)和牙本质涎磷蛋白(DSPP)基因的高表达水平。结果突出了不同支架比例对细胞微环境的影响,并表明BCP20支架可以支持HDPC分化用于牙本质组织再生。