Bakhtiar H, Mirzaei H, Bagheri M R, Fani N, Mashhadiabbas F, Baghaban Eslaminejad M, Sharifi D, Nekoofar M H, Dummer Pmh
Dental Material Research Center, Tehran Dental Branch, Islamic Azad University, Tehran, Iran.
Department of Stem Cells and Developmental Biology, Cell Sciences Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Clin Oral Investig. 2017 Jun;21(5):1579-1588. doi: 10.1007/s00784-016-1967-0. Epub 2016 Oct 20.
The aim of this study is to compare the effect of treated dentine matrix (TDM) and tricalcium phosphate (TCP) scaffolds on odontogenic differentiation and mineralization of dental pulp stem cells (DPSCs) in furcation perforations created in the pulp chamber floor of premolar teeth in dogs.
DPSCs were isolated and cultured from the dental pulp of the maxillary left second and third premolars of dogs. The DPSCs were loaded on TCP (SC+TCP) and TDM (SC+TDM) scaffolds and inserted into intentionally perforated pulp chamber floors of premolars in dogs; six teeth were used for each group. Three more groups of six specimens were created, and mineral trioxide aggregate (MTA), TDM, and TCP were inserted into the perforations to act as controls. An intact premolar and no treatment in the perforation site were used as positive and negative controls respectively. After 3 months, the animals were sacrificed and the type of inflammation, presence of dentine, continuation and type of cementum, type of connective tissue, and presence of foreign body reaction were evaluated, and significant differences were between groups determined using the Fisher's exact test. The evaluation of the amount of inflammation and the percentage of new bone formation was evaluated using the Mann-Whitney U test.
The negative control group was associated with severe inflammation and granulation tissue formation. In the positive control group, intact periodontal tissues and no inflammation were observed. Dentine bridge formation was not seen in specimens of any group. The specimens in the SC+TDM group were associated with significantly more bone formation than other groups (P < 0.001). The amount of inflammation was less than 10 % in specimens of all groups with the exception of three specimens in the TCP group that were categorized as 10-30 %. Chronic inflammation without foreign body reactions was the major pattern of inflammation in groups. Formation of cementum with a cellular and continuous appearance was seen in all specimens.
SC+TDM was associated with significantly more bone formation when used to repair uninfected furcation perforations in the premolar teeth of dogs.
Application of TDM as a biological scaffold in combination with DPSCs may offer an advantage during the repair of root perforation defects.
本研究旨在比较处理后的牙本质基质(TDM)和磷酸三钙(TCP)支架对犬前磨牙牙髓腔底部根分叉穿孔处牙髓干细胞(DPSC)牙源性分化和矿化的影响。
从犬左上第二和第三前磨牙的牙髓中分离并培养DPSC。将DPSC接种于TCP(SC+TCP)和TDM(SC+TDM)支架上,并植入犬前磨牙故意穿孔的牙髓腔底部;每组使用6颗牙齿。另外创建三组,每组6个标本,将矿物三氧化物凝聚体(MTA)、TDM和TCP植入穿孔处作为对照。完整的前磨牙和穿孔部位不做处理分别作为阳性和阴性对照。3个月后,处死动物,评估炎症类型、牙本质的存在、牙骨质的延续和类型、结缔组织类型以及异物反应的存在,并使用Fisher精确检验确定组间的显著差异。使用Mann-Whitney U检验评估炎症量和新骨形成百分比。
阴性对照组伴有严重炎症和肉芽组织形成。阳性对照组观察到完整的牙周组织且无炎症。任何组的标本中均未见到牙本质桥形成。SC+TDM组的标本与其他组相比,骨形成明显更多(P<0.001)。除TCP组的3个标本炎症量为10%-30%外,所有组标本的炎症量均小于10%。慢性炎症且无异物反应是各组炎症的主要模式。所有标本中均可见到细胞性且连续的牙骨质形成。
当用于修复犬前磨牙未感染的根分叉穿孔时,SC+TDM与明显更多的骨形成相关。
将TDM作为生物支架与DPSC联合应用可能在根穿孔缺损修复过程中具有优势。