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Dikkopf-1 promotes matrix mineralization of osteoblasts by regulating Ca+-CAMK2A-CREB1 pathway

机译:Dikkopf-1 通过调节 Ca+-CAMK2A-CREB1 通路促进成骨细胞基质矿化

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摘要

Dickkopf-1 (DKK1) is a secreted protein that acts as an antagonist of the canonical WNT/β-catenin pathway, which regulates osteoblast differentiation. However, the role of DKK1 on osteoblast differentiation has not yet been fully clarified. Here, we investigate the functional role of DKK1 on osteoblast differentiation. Primary osteoprogenitor cells were isolated from human spinal bone tissues. To examine the role of DKK1 in osteoblast differentiation, we manipulated the expression of DKK1, and the cells were differentiated into mature osteoblasts. DKK1 overexpression in osteoprogenitor cells promoted matrix mineralization of osteoblast differentiation but did not promote matrix maturation. DKK1 increased Ca+ influx and activation of the Ca+/calmodulin-dependent protein kinase II Alpha (CAMK2A)-cAMP response element-binding protein 1 (CREB1) and increased translocation of p-CREB1 into the nucleus. In contrast, stable DKK1 knockdown in human osteosarcoma cell line SaOS2 exhibited reduced nuclear translocation of p-CREB1 and matrix mineralization. Overall, we suggest that manipulating DKK1 regulates the matrix mineralization of osteoblasts by Ca+-CAMK2A-CREB1, and DKK1 is a crucial gene for bone mineralization of osteoblasts.
机译:Dickkopf-1 (DKK1) 是一种分泌蛋白,可作为经典 WNT/β-catenin 通路的拮抗剂,调节成骨细胞分化。然而,DKK1 对成骨细胞分化的作用尚未完全阐明。在这里,我们研究了 DKK1 对成骨细胞分化的功能作用。从人脊髓骨组织中分离出原代骨祖细胞。为了检查 DKK1 在成骨细胞分化中的作用,我们操纵了 DKK1 的表达,并将细胞分化为成熟的成骨细胞。DKK1 在骨祖细胞中过表达促进了成骨细胞分化的基质矿化,但不促进基质成熟。DKK1 增加了 Ca+/钙调蛋白依赖性蛋白激酶 II α (CAMK2A)-cAMP 反应元件结合蛋白 1 (CREB1) 的内流和激活,并增加了 p-CREB1 向细胞核的易位。相比之下,人骨肉瘤细胞系 SaOS2 中稳定的 DKK1 敲低表现出 p-CREB1 核转位和基质矿化减少。总体而言,我们认为操纵 DKK1 通过 Ca+-CAMK2A-CREB1 调节成骨细胞基质矿化,DKK1 是成骨细胞骨矿化的关键基因。

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