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首页> 外文期刊>Developmental cell >Synaptotagmin VII regulates bone remodeling by modulating osteoclast and osteoblast secretion.
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Synaptotagmin VII regulates bone remodeling by modulating osteoclast and osteoblast secretion.

机译:Synaptotagmin VII通过调节破骨细胞和成骨细胞分泌来调节骨重塑。

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摘要

Maintenance of bone mass and integrity requires a tight balance between resorption by osteoclasts and formation by osteoblasts. Exocytosis of functional proteins is a prerequisite for the activity of both cells. In the present study, we show that synaptotagmin VII, a calcium sensor protein that regulates exocytosis, is associated with lysosomes in osteoclasts and bone matrix protein-containing vesicles in osteoblasts. Absence of synaptotagmin VII inhibits cathepsin K secretion and formation of the ruffled border in osteoclasts and bone matrix protein deposition in osteoblasts, without affecting the differentiation of either cell. Reflecting these in vitro findings, synaptotagmin VII-deficient mice are osteopenic due to impaired bone resorption and formation. Therefore, synaptotagmin VII plays an important role in bone remodeling and homeostasis by modulating secretory pathways functionally important in osteoclasts and osteoblasts.
机译:维持骨量和完整性需要破骨细胞吸收与成骨细胞形成之间的紧密平衡。功能蛋白的胞吐作用是两个细胞活性的先决条件。在本研究中,我们显示突触结合蛋白VII(一种调节胞吐作用的钙传感器蛋白)与破骨细胞中的溶酶体和成骨细胞中含有骨基质蛋白的囊泡有关。没有突触结合蛋白VII抑制组织蛋白酶K的分泌和破骨细胞中皱纹边界的形成以及成骨细胞中骨基质蛋白的沉积,而不会影响任何一个细胞的分化。反映这些体外研究结果,由于缺乏骨吸收和形成,突触小蛋白VII缺乏症小鼠骨质疏松。因此,突触结合蛋白VII通过调节在破骨细胞和成骨细胞中功能重要的分泌途径,在骨重塑和体内平衡中发挥重要作用。

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