Koga Takamitsu, Minamizato Tokutaro, Kawai Yosuke, Miura Kei-ichiro, I Takashi, Nakatani Yuya, Sumita Yoshinori, Asahina Izumi
Department of Regenerative Oral Surgery, Unit of Translational Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
PLoS One. 2016 Jan 21;11(1):e0147235. doi: 10.1371/journal.pone.0147235. eCollection 2016.
This study aimed to examine the influence of particle size and extent of demineralization of dentin matrix on bone regeneration.
Extracted human teeth were pulverized and divided into 3 groups according to particle size; 200, 500, and 1000 μm. Each group was divided into 3 groups depending on the extent of demineralization; undemineralized dentin (UDD), partially demineralized dentin matrix (PDDM), and completely demineralized dentin matrix (CDDM). The dentin sample was implanted into rat calvarial bone defects. After 4 and 8 weeks, the bone regeneration was evaluated with micro-CT images, histomorphometric and immunohistochemical analyses. Osteoblasts were cultured on UDD and DDM to evaluate the cell attachment using electron microscope.
Micro-CT images and histological observation revealed that CDDM had largely resorbed but UDD had not, and both of them induced little bone formation, whereas all particle sizes of PDDM induced more new bone, especially the 1000 μm. Electron microscopic observation showed osteoblasts attached to DDM but not to UDD.
PDDM with larger particle size induced prominent bone regeneration, probably because PDDM possessed a suitable surface for cell attachment. There might be an exquisite balance between its resorption and bone formation on it. PDDM could be considered as a potential bone substitute.
本研究旨在探讨牙本质基质的颗粒大小和脱矿程度对骨再生的影响。
将拔除的人牙粉碎,并根据颗粒大小分为3组;200、500和1000μm。每组根据脱矿程度再分为3组;未脱矿牙本质(UDD)、部分脱矿牙本质基质(PDDM)和完全脱矿牙本质基质(CDDM)。将牙本质样本植入大鼠颅骨骨缺损处。4周和8周后,通过显微CT图像、组织形态计量学和免疫组织化学分析评估骨再生情况。将成骨细胞培养在UDD和DDM上,使用电子显微镜评估细胞附着情况。
显微CT图像和组织学观察显示,CDDM已大量吸收,但UDD未吸收,且两者均诱导少量骨形成,而所有颗粒大小的PDDM均诱导更多新骨形成,尤其是1000μm的PDDM。电子显微镜观察显示成骨细胞附着于DDM而非UDD。
较大颗粒大小的PDDM诱导显著的骨再生,可能是因为PDDM具有适合细胞附着的表面。其吸收与骨形成之间可能存在精确的平衡。PDDM可被视为一种潜在的骨替代物。