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黑素皮质素-2 受体及其辅助蛋白在发育中和成年肾上腺中的定位。

Localisation of the melanocortin-2-receptor and its accessory proteins in the developing and adult adrenal gland.

机构信息

William Harvey Research Institute, Centre for Endocrinology, Queen Mary University of London, Barts and The London School of Medicine and Dentistry, London EC1M 6BQ, UK.

出版信息

J Mol Endocrinol. 2011 Jun 9;46(3):227-32. doi: 10.1530/JME-11-0011. Print 2011 Jun.

Abstract

The melanocortin-2-receptor (MC2R)/MC2R accessory protein (MRAP) complex is critical to the production of glucocorticoids from the adrenal cortex. Inactivating mutations in either MC2R or MRAP result in the clinical condition familial glucocorticoid deficiency. The localisation of MC2R together with MRAP within the adrenal gland has not previously been reported. Furthermore, MRAP2, a paralogue of MRAP, has been shown in vitro to have a similar function to MRAP, facilitating MC2R trafficking and responsiveness to ACTH. Despite similar MC2R accessory functions, in vivo, patients with inactivating mutations of MRAP fail to be rescued by a functioning MRAP2 gene, suggesting differences in adrenal expression, localisation and/or function between the two MRAPs. In this study on the rat adrenal gland, we demonstrate that while MRAP and MC2R are highly expressed in the zona fasciculata, MRAP2 is expressed throughout the adrenal cortex in low quantities. In the developing adrenal gland, both MRAP and MRAP2 are equally well expressed. The MC2R/MRAP2 complex requires much higher concentrations of ACTH to activate compared with the MC2R/MRAP complex. Interestingly, expression of MC2R and MRAP in the undifferentiated zone would support the notion that ACTH may play an important role in adrenal cell differentiation and maintenance.

摘要

黑素皮质素 2 受体(MC2R)/MC2R 辅助蛋白(MRAP)复合物对于肾上腺皮质产生糖皮质激素至关重要。MC2R 或 MRAP 中的失活突变会导致家族性糖皮质激素缺乏症的临床病症。MC2R 与 MRAP 在肾上腺内的定位以前尚未报道过。此外,MRAP 的一种旁系同源物 MRAP2 在体外已被证明具有类似的功能,促进 MC2R 的运输和对 ACTH 的反应性。尽管具有相似的 MC2R 辅助功能,但在体内,MRAP 失活突变的患者不能被功能正常的 MRAP2 基因拯救,这表明两种 MRAP 之间在肾上腺表达、定位和/或功能上存在差异。在这项关于大鼠肾上腺的研究中,我们证明了尽管 MRAP 和 MC2R 在束状带中高度表达,但 MRAP2 在整个肾上腺皮质中以低量表达。在发育中的肾上腺中,MRAP 和 MRAP2 的表达水平相当。与 MC2R/MRAP 复合物相比,MC2R/MRAP2 复合物需要更高浓度的 ACTH 才能被激活。有趣的是,未分化区 MC2R 和 MRAP 的表达支持 ACTH 可能在肾上腺细胞分化和维持中发挥重要作用的观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2db9/3111094/2dcae3d1472a/JME110011f01.jpg

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