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Osteoblast migration into type I collagen gel and differentiation to osteocyte-like cells within a self-produced mineralized matrix: A novel system for analyzing differentiation from osteoblast to osteocyte

机译:成骨细胞迁移到I型胶原凝胶中并在自生矿化基质中分化为骨细胞样细胞:一种新型系统,用于分析从成骨细胞到骨细胞的分化

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Osteoblasts are believed to differentiate into osteocytes, becoming embedded in bone, or to undergo apoptosis after the bone formation phase. The regulation of this terminal differentiation seems to be critical for bone homeostasis. However the mechanism remains unclear and there is no assay system currently available to analyze this process. To address this issue, we developed a new model in which osteoblasts are cultured on a type I collagen gel layer with osteogenic supplements β-glycerophosphate and ascorbic acid. Cellular behavior was analyzed by electron microscopy, immunohistochemistry and real-time RT-PCR. Osteoblasts gradually migrated into the gel, produced collagen fibrils, and differentiated to osteocytic cells with bone lacunae- and canaliculi-like mineralization. Osteocalcin, DMP-1 and SOST protein expression was mainly expressed in the migrated cells within the mid-layer of the gel. Osteoblastic (ALP and osteocalcin) and osteocytic (PHEX, DMP-1 and SOST) mRNA expression was significantly increased compared with those of the cells cultured on plastic dishes alone after 21. days. The number of TUNEL-positive apoptotic cells gradually increased, reaching a maximum at 28. days. The cells were distributed at the surface and in the mid-layer of the gel at 7. days and after 14. days of culture, respectively. These data indicate that our model reproduces transition from osteoblasts to osteocytes, suggesting the following: 1) migration of osteoblasts into collagen gel may play a critical role in osteocytic differentiation; and 2) spatiotemporal gene expression and apoptosis may be involved in the terminal differentiation of osteoblasts. Our model will make it possible to study the mechanism of transition from osteoblast to osteocyte, and both cell type-related diseases including osteoporosis and osteonecrosis.
机译:据信成骨细胞分化为骨细胞,嵌入骨中,或在骨形成阶段后发生凋亡。这种终末分化的调节似乎对于骨稳态是至关重要的。然而,机制仍不清楚,目前没有可用于分析该过程的测定系统。为了解决这个问题,我们开发了一种新模型,其中将成骨细胞培养在具有成骨性补品β-甘油磷酸和抗坏血酸的I型胶原凝胶层上。通过电子显微镜,免疫组织化学和实时RT-PCR分析细胞行为。成骨细胞逐渐迁移到凝胶中,产生胶原原纤维,并分化成具有骨腔和小管样矿物质的骨细胞。骨钙素,DMP-1和SOST蛋白的表达主要在凝胶中层内的迁移细胞中表达。与21天后单独在塑料皿上培养的细胞相比,成骨细胞(ALP和骨钙素)和骨细胞(PHEX,DMP-1和SOST)mRNA表达显着增加。 TUNEL阳性凋亡细胞的数量逐渐增加,在28天时达到最大值。培养分别在第7天和第14天后,将细胞分布在凝胶的表面和中层。这些数据表明我们的模型再现了从成骨细胞到成骨细胞的转变,表明以下内容:1)成骨细胞向胶原凝胶的迁移可能在成骨细胞分化中起关键作用; 2)时空基因的表达和凋亡可能与成骨细胞的终末分化有关。我们的模型将使研究成骨细胞向骨细胞转变的机制以及包括骨质疏松和骨坏死在内的两种与细胞类型相关的疾病成为可能。

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