Pilbauerova Nela, Dasi Divyamaanasa, de Souza Araujo Isaac J, Huang George T-J
Department of Bioscience Research, College of Dentistry, University of Tennessee Health Science Center, Memphis, Tennessee; Department of Dentistry, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic; Department of Dentistry, Faculty of Medicine in Hradec Kralove, Charles University, Hradec Kralove, Czech Republic.
Department of Bioscience Research, College of Dentistry, University of Tennessee Health Science Center, Memphis, Tennessee.
J Endod. 2025 Aug;51(8):1072-1080. doi: 10.1016/j.joen.2025.04.018. Epub 2025 May 9.
Cell-based pulp regeneration utilizes capping materials underneath a final restoration to seal the tooth after delivering cells into the canal system. Studying the immediate biocompatibility of materials with injected cells has been challenging. This study aimed to utilize a tube model to observe cell response directly and conveniently to the capping materials in a cell culture in vitro system.
A tapered plastic tube (14 mm in length, 2 mm diameter of the apex opening) to simulate root canal space was filled with fluorescence-labeled dental pulp cells mixed in fibrin gel and the larger end sealed with various capping materials including Mineral Trioxide Aggregate (MTA), Biodentine, hydroxyapatite-tricalcium phosphate (HA-TCP), composite, and glass ionomer. The tube was placed in wells of culture plates and incubated for various times in vitro and observed under the microscope for cell morphological changes. pH changes within the tube were monitored over time.
Both fresh MTA and Biodentine caused adverse response to the cells in the tube. Only a few normally growing cells were observed at the apical end. Composite or glass ionomer appeared better tolerated by cells. HA-TCP mixed in fibrin gel demonstrated the highest compatibility with cells; however, using HA-TCP to separate cells from fresh MTA or Biodentine did not reduce the negative effect of these 2 calcium silicate cements. The pH increased within the tube may explain the observed toxicity.
Using HA-TCP mixed in fibrin gel as a capping material appears highly biocompatible to cells while fresh MTA and Biodentine are not.
基于细胞的牙髓再生是在最终修复体下方使用盖髓材料,在将细胞输送到根管系统后封闭牙齿。研究材料与注入细胞的即时生物相容性一直具有挑战性。本研究旨在利用管模型在体外细胞培养系统中直接且方便地观察细胞对盖髓材料的反应。
用模拟根管空间的锥形塑料管(长度14毫米,根尖开口直径2毫米),填充混合在纤维蛋白凝胶中的荧光标记牙髓细胞,较大一端用包括三氧化矿物凝聚体(MTA)、生物活性玻璃陶瓷(Biodentine)、羟基磷灰石-磷酸三钙(HA-TCP)、复合树脂和玻璃离子水门汀在内的各种盖髓材料密封。将管子置于培养板孔中,在体外孵育不同时间,并在显微镜下观察细胞形态变化。随时间监测管内pH值变化。
新鲜的MTA和Biodentine对管内细胞均产生不良反应。仅在根尖末端观察到少数正常生长的细胞。复合树脂或玻璃离子水门汀似乎更能被细胞耐受。纤维蛋白凝胶中混合的HA-TCP与细胞表现出最高的相容性;然而,使用HA-TCP将细胞与新鲜的MTA或Biodentine隔开并不能降低这两种硅酸钙水门汀的负面影响。管内pH值升高可能解释了观察到的毒性。
使用纤维蛋白凝胶中混合的HA-TCP作为盖髓材料似乎对细胞具有高度生物相容性,而新鲜的MTA和Biodentine则不然。