FKBP51 and the molecular chaperoning of metabolism.

FKBP51 and the molecular chaperoning of metabolism.
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DOI:
10.1016/j.tem.2021.08.003
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发表时间:
2021-11
期刊:
Trends in endocrinology and metabolism: TEM
影响因子:
--
通讯作者:
Hinds TD Jr
Hinds TD Jr
中科院分区:
其他
文献类型:
--
作者:
Smedlund KB;Sanchez ER;Hinds TD Jr

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分子伴侣FKBP51作为代谢功能障碍的有意义的生物标志物正受到关注。本文综述了FKBP51在脂肪形成和脂质代谢、肌肉形成和蛋白质分解代谢以及糖皮质激素诱导的皮肤发育不全和真皮脂肪细胞中的新贡献。讨论了可能解释这些代谢后果的FKBP51信号传导机制。这些机制是多种多样的,FKBP51独立和直接调节磷酸化级联反应和核受体。我们提供了一个新开发的化合物,拮抗FKBP51,可能提供治疗肥胖的优势的讨论。这些观察结果表明,我们才刚刚开始揭示FKBP51的复杂性质及其代谢的分子陪伴。
The molecular chaperone FKBP51 is gaining attention as a meaningful biomarker of metabolic dysfunction. This review examines the emerging contributions of FKBP51 in adipogenesis and lipid metabolism, myogenesis and protein catabolism, and glucocorticoid-induced skin hypoplasia and dermal adipocytes. The FKBP51 signaling mechanisms that may explain these metabolic consequences are discussed. These mechanisms are diverse, with FKBP51 independently and directly regulating phosphorylation cascades and nuclear receptors. We provide a discussion of the newly developed compounds that antagonize FKBP51, which may offer therapeutic advantages for adiposity. These observations suggest we are only beginning to uncover the complex nature of FKBP51 and its molecular chaperoning of metabolism.
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