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Proliferation, apoptosis and expression of non-collagenous proteins: Differences between the upper and the lower jaw bone in vitro

机译:非胶原蛋白的增殖,凋亡和表达:上颌骨和下颌骨的体外差异

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One of the effects observed during several screening studies for osteocompatibility in vitro was that cells derived from the upper and lower jaw exhibited distinct differences regarding proliferation. Therefore, the aim of this study was to examine systematically whether a single osteoblast possesses abilities which are specific to the upper or lower jaw. Both human maxillary and mandibular bone samples without any clinical or radiographic evidence of pathology were obtained from 4 male donors aged between 40 and 45 years. Cells were cultured for up to 25 days to investigate in vitro development. Total and apoptotic cell numbers were estimated by image analysis. Cells were identified as bone-like cells using immunocytochemical determination of bone sialoprotein (BSP) and osteocalcin expression. The number of healthy cells was significantly higher for cells of the lower jaw compared to those of the upper jaw. The number of apoptotic cells showed an inverse pattern. The expression pattern of osseo-inductive BSP correlated with the proliferation rate of the cells. The pattern of osteocalcin expression was related to the number of apoptotic cells. Our findings are new but were anticipated regarding the well-known differences in the healing process around implants in the lower jaw versus the upper jaw. Additionally, a relationship between our results and some diseases of the lower/upper jaw seems obvious. Future work on cell responses to biomaterials should define the origin of the cells more precisely.
机译:在几次体外骨相容性筛选研究中观察到的效果之一是,来自上颌骨和下颌骨的细胞在增殖方面表现出明显差异。因此,本研究的目的是系统地检查单个成骨细胞是否具有特定于上颌或下颌的能力。从4名年龄在40至45岁之间的男性供体中获得了没有任何病理学临床或影像学证据的人上颌骨和下颌骨样品。将细胞培养长达25天,以研究体外发育。通过图像分析估计总和凋亡细胞数。使用免疫细胞化学法测定骨唾液蛋白(BSP)和骨钙素的表达,将细胞鉴定为骨样细胞。下颌细胞的健康细胞数量明显高于上颌细胞。凋亡细胞的数量显示相反的模式。骨诱导性BSP的表达模式与细胞的增殖速率相关。骨钙素的表达方式与凋亡细胞的数量有关。我们的发现是新的,但可以预料到下颌骨与上颌骨种植体周围愈合过程的众所周知差异。此外,我们的结果与下颌上颌某些疾病之间的关系似乎很明显。关于细胞对生物材料的反应的未来工作应更精确地定义细胞的起源。

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