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Withdrawal of parathyroid hormone after prolonged administration leads to adipogenic differentiation of mesenchymal precursors in vivo

机译:延长施用后脱甲酸甲状腺素激素导致体内间充质前体的脂肪生成分化

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摘要

Intermittent PTH-like drugs are the only approved so-called anabolic agent that increases bone mass in both mice and humans. It is well documented that PTH targets mature cells of the osteoblast lineage, with only indirect evidence of its actions on early cells of the osteoblast lineage. Using a triple transgenic mouse model that allowed labeling of very early cells of the osteoblast lineage, we traced the progeny of these into osteoblast lineage in adult mice. These early cells expressed PTH1R and multiplied when PTH (1–34) was administered daily. We also showed that the early mesenchymal cells showed accelerated differentiation into mature osteocalcin-positive osteoblasts and osteocytes. Rather surprisingly, when teriparatide administration was stopped, these early mesenchymal precursors differentiated into adipocytes. We showed that the adipogenic differentiation is accompanied by a decrease in wnt signaling in osteoblast precursors. In this review, we discuss the possible clinical relevance of this finding and the possible molecular mechanisms that contribute to this phenotypein vivo.
机译:间歇性pth样药是唯一批准的所谓的代谢剂,可以增加小鼠和人类的骨质。有很好的记录结果,PTH靶向成骨细胞谱系的成熟细胞,只有间接证据对成骨细胞谱系的早期细胞的动作。使用三重转基因小鼠模型,允许标记成骨细胞谱系的非常早期的细胞,我们将这些中的血管谱系追溯到成人小鼠中的成骨细胞谱系。这些早期细胞表达PTH1R并在每日施用PTH(1-34)时乘以。我们还表明,早期间充质细胞显示成加速分化为成熟的骨屈曲阳性成骨细胞和骨细胞。令人惊讶的是,当停止萜酰基氮酰胺给药时,这些早期间充质前体分化为脂肪细胞。我们表明,脂肪生成分化伴随着骨盆前体中Wnt信号传导的减少。在本综述中,我们讨论了这种发现的可能临床意义和有助于这种现象脂体内的可能的分子机制。

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