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首页> 外文期刊>General and comparative endocrinology >Involvement of melanocortin receptor accessory proteins (MRAPs) in the function of melanocortin receptors.
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Involvement of melanocortin receptor accessory proteins (MRAPs) in the function of melanocortin receptors.

机译:黑皮质素受体辅助蛋白(MRAP)参与黑皮质素受体的功能。

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摘要

The melanocortin system integrates different agonists, competitive or inverse agonists, and receptors. Recent investigations have also discovered a specific system of melanocortin receptor accessory proteins (MRAPs) that are involved in the regulation of the functional expression of these receptors. MRAP1 mutations are responsible for type 2 familial glucocorticoid deficiency (FGD2), a rare autosomal disorder characterized by high plasma adrenocorticotropin hormone (ACTH) levels but severe cortisol deficiency. ACTH binds melanocortin 2 receptor (MC2R), a G protein-coupled receptor, in the adrenal gland to promote corticosteroid synthesis. In the absence of MRAP1, MC2R cannot translocate from the endoplasmic reticulum to the plasma membrane and ACTH-induced signaling is extinguished. A second MRAP protein, called MRAP2, also modulates MC2R activity. MRAPs also interact with the other melanocortin receptors, adjusting their pharmacological properties. In this paper, we briefly review the MRAP system and its interaction with melanocortin receptors.
机译:黑皮质素系统整合了不同的激动剂,竞争性或反向激动剂和受体。最近的研究还发现了黑皮皮质素受体辅助蛋白(MRAP)的特定系统,该系统参与调节这些受体的功能性表达。 MRAP1突变是造成2型家族性糖皮质激素缺乏症(FGD2)的原因,FGD2是一种罕见的常染色体疾病,其特征在于血浆肾上腺皮质激素(ACTH)水平高但皮质醇严重缺乏。 ACTH在肾上腺中结合G蛋白偶联受体melanocortin 2受体(MC2R),以促进皮质类固醇合成。在缺少MRAP1的情况下,MC2R无法从内质网转移到质膜,并且ACTH诱导的信号传导被消除。第二种MRAP蛋白,称为MRAP2,也调节MC2R活性。 MRAP还与其他黑皮质素受体相互作用,从而调节其药理特性。在本文中,我们简要回顾了MRAP系统及其与黑皮质素受体的相互作用。

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