The role of receptor activity-modifying proteins in obesity and diabetes mellitus

IF 3.6 4区 医学 Q2 ENDOCRINOLOGY & METABOLISM Journal of molecular endocrinology Pub Date : 2024-09-01 DOI:10.1530/jme-24-0056
Milena A Malcharek, Abigail Pearce, Cheryl A Brighton, David C Hornigold, Graham Ladds
{"title":"The role of receptor activity-modifying proteins in obesity and diabetes mellitus","authors":"Milena A Malcharek, Abigail Pearce, Cheryl A Brighton, David C Hornigold, Graham Ladds","doi":"10.1530/jme-24-0056","DOIUrl":null,"url":null,"abstract":"<p>Receptor activity-modifying proteins (RAMPs) modulate the expression and activity of numerous G protein-coupled receptors, primarily those within class B1. These receptors have important physiological roles, including in the regulation of food intake, energy metabolism, and glucose homeostasis. Dysregulation of these pathways can lead to obesity and diabetes mellitus, which present an ever-expanding global challenge. Whilst the roles of class B1 receptors and their peptide agonists in obesity and diabetes have been investigated, the contribution of RAMPs is less well understood. This review summarises the results of RAMP knockout studies, highlighting the involvement of these proteins in the incidence of disease. It then moves to discuss how receptor, RAMP, and agonist expression changes in disease states, and the benefits (or detriments) of these agonists to the pathways implicated in disease pathophysiology. Whilst much of the data centres around the calcitonin family of receptors, as their interactions with RAMPs are well established, this review then discusses receptors whose role in obesity and diabetes is well founded, but the significance of whose interactions with RAMPs is more recently emerging. The conclusion of this study of the literature is, however, that the information surrounding RAMPs is conflicting and multifaceted, and more research is required to fully understand their contribution to obesity and diabetes.</p>","PeriodicalId":16570,"journal":{"name":"Journal of molecular endocrinology","volume":"39 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of molecular endocrinology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1530/jme-24-0056","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

Abstract

Receptor activity-modifying proteins (RAMPs) modulate the expression and activity of numerous G protein-coupled receptors, primarily those within class B1. These receptors have important physiological roles, including in the regulation of food intake, energy metabolism, and glucose homeostasis. Dysregulation of these pathways can lead to obesity and diabetes mellitus, which present an ever-expanding global challenge. Whilst the roles of class B1 receptors and their peptide agonists in obesity and diabetes have been investigated, the contribution of RAMPs is less well understood. This review summarises the results of RAMP knockout studies, highlighting the involvement of these proteins in the incidence of disease. It then moves to discuss how receptor, RAMP, and agonist expression changes in disease states, and the benefits (or detriments) of these agonists to the pathways implicated in disease pathophysiology. Whilst much of the data centres around the calcitonin family of receptors, as their interactions with RAMPs are well established, this review then discusses receptors whose role in obesity and diabetes is well founded, but the significance of whose interactions with RAMPs is more recently emerging. The conclusion of this study of the literature is, however, that the information surrounding RAMPs is conflicting and multifaceted, and more research is required to fully understand their contribution to obesity and diabetes.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
受体活性修饰蛋白在肥胖症和糖尿病中的作用
受体活性修饰蛋白(RAMPs)可调节多种 G 蛋白偶联受体(主要是 B1 类受体)的表达和活性。这些受体具有重要的生理作用,包括调节食物摄入、能量代谢和葡萄糖稳态。这些途径的失调可导致肥胖症和糖尿病,是一个日益严重的全球性挑战。虽然人们已经研究了 B1 类受体及其多肽激动剂在肥胖和糖尿病中的作用,但对 RAMPs 的作用却不甚了解。本综述总结了 RAMP 基因敲除研究的结果,强调了这些蛋白与疾病发生的关系。然后讨论了受体、RAMP 和激动剂的表达在疾病状态下的变化,以及这些激动剂对疾病病理生理学途径的益处(或害处)。由于降钙素家族受体与 RAMPs 的相互作用已得到充分证实,因此大部分数据都以降钙素家族受体为中心;本综述随后讨论了在肥胖症和糖尿病中的作用已得到充分证实,但其与 RAMPs 相互作用的重要性最近才逐渐显现的受体。然而,本文献研究的结论是,围绕 RAMPs 的信息是相互矛盾和多方面的,需要进行更多的研究才能充分了解它们对肥胖和糖尿病的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of molecular endocrinology
Journal of molecular endocrinology 医学-内分泌学与代谢
CiteScore
6.90
自引率
0.00%
发文量
96
审稿时长
1 months
期刊介绍: The Journal of Molecular Endocrinology is an official journal of the Society for Endocrinology and is endorsed by the European Society of Endocrinology and the Endocrine Society of Australia. Journal of Molecular Endocrinology is a leading global journal that publishes original research articles and reviews. The journal focuses on molecular and cellular mechanisms in endocrinology, including: gene regulation, cell biology, signalling, mutations, transgenics, hormone-dependant cancers, nuclear receptors, and omics. Basic and pathophysiological studies at the molecule and cell level are considered, as well as human sample studies where this is the experimental model of choice. Technique studies including CRISPR or gene editing are also encouraged.
期刊最新文献
Emerging roles of osteocytes in the regulation of bone and skeletal muscle mass. The role of mu-opioid receptors in pancreatic islet α-cells. Syndecans modulate ghrelin receptor signaling. Continuing the success of Journal of Endocrinology and Journal of Molecular Endocrinology: Editor-in-Chief handover. ATF3 suppresses 3T3-L1 adipocyte adipogenesis via transcriptional repressing USP53.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1