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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:黑素旋素受体辅助蛋白(MRAPS)在黑素旋蛋白受体的作用中的参与。

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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:Melanocortin系统将不同的激动剂,竞争或反向激动剂和受体整合。最近的研究还发现了涉及这些受体功能表达的调节的Melanocortin受体辅助蛋白(MRAPS)的特定系统。 MRAP1突变对2型家族性糖皮质激素缺乏(FGD2)负责,一种稀有的常血型疾病,其特征在于高血浆肾上腺皮质激素激素(ACTH)水平,但严重的皮质醇缺乏。 Acth在肾上腺中结合黑色素体2受体(MC2R),G蛋白偶联受体,以促进皮质类固醇合成。在没有MRAP1的情况下,MC2R不能从内质网转移到质膜,并且诱导的信号传导熄灭。第二MRAP蛋白,称为MRAP2,也调节MC2R活性。 MRAP也与其他黑色主酶受体相互作用,调节其药理性质。在本文中,我们简要介绍了MRAP系统及其与黑素旋蛋白受体的相互作用。

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