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Leptin synergizes with thyroid hormone signaling in promoting growth plate chondrocyte proliferation and terminal differentiation in vitro.

机译:瘦素与甲状腺激素信号传导在体外促进生长板软骨细胞增殖和终末分化。

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摘要

Leptin and thyroid hormone are two hormones that regulate energy balance through central signaling mechanisms. Recent studies in leptin-deficient ob/ob mice indicate that leptin also has peripheral effects in modulating the function of the growth plate, perhaps in terms of proliferation and differentiation enhancement. Thyroid hormone has been well-described as a potent stimulator of growth plate chondrocyte maturation. The objective of this study was therefore to investigate the interaction between leptin and thyroid hormone signaling in growth plate chondrocyte proliferation and terminal differentiation. Our in vitro data demonstrate that leptin synergistically functions with thyroid hormone through activation of both IGF-1/IGF1R signaling and Wnt/beta-catenin signaling, two pathways that have been previously described as downstream effectors of thyroid hormone action. Leptin increases thyroid hormone receptor-alpha (TRalpha) expression and thyroid hormone receptor transcriptional activity. Thyroid hormone also activates leptin signaling in growth plate cells undergoing proliferation and hypertrophy. We conclude that leptin synergically interacts with thyroid hormone in promoting growth plate chondrocyte proliferation and terminal differentiation.
机译:瘦素和甲状腺激素是通过中枢信号传导机制调节能量平衡的两种激素。瘦素缺陷型ob / ob小鼠的最新研究表明,瘦素在调节生长板的功能方面可能也具有外围作用,也许就增殖和分化增强而言。众所周知,甲状腺激素是生长板软骨细胞成熟的有效刺激剂。因此,本研究的目的是研究瘦素与甲状腺激素信号在生长板软骨细胞增殖和终末分化中的相互作用。我们的体外数据表明,瘦素通过激活IGF-1 / IGF1R信号传导和Wnt /β-catenin信号传导与甲状腺激素协同作用,这两个途径先前已被描述为甲状腺激素作用的下游效应器。瘦素增加甲状腺激素受体-α(TRalpha)的表达和甲状腺激素受体的转录活性。甲状腺激素还激活经历增殖和肥大的生长板细胞中的瘦素信号传导。我们得出的结论是,瘦素与甲状腺激素协同作用,促进生长板软骨细胞增殖和终末分化。

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