{"title":"Chemokine receptors - Exemplifying functional divergence in G protein-coupled receptors.","authors":"Omolade Otun, Sébastien Granier, Thierry Durroux, Cherine Bechara","doi":"10.1016/j.molpha.2025.100053","DOIUrl":null,"url":null,"abstract":"<p><p>G protein-coupled receptors are known for their ability to generate a wide range of functional responses through interaction with various intracellular partners. This versatility is particularly evident within the chemokine receptor family, where conventional receptors signal primarily through classic G protein-coupled pathways while atypical chemokine receptors appear not to possess such ability but instead couple to alternative intracellular partners such as β-arrestins. Functional diversity in signaling presents unique opportunities for drug development, allowing different pathways to be selectively targeted to meet specific therapeutic needs. This minireview explores the mechanisms by which G protein-coupled receptor signaling, particularly within the chemokine receptor family, can be diversified at the modulatory, transmembrane, and intracellular levels. SIGNIFICANCE STATEMENT: This minireview explores how signaling in the chemokine receptor family diversifies at the ligand, transmembrane, and intracellular levels. This functional diversity presents unique opportunities for drug development by selectively targeting distinct pathways.</p>","PeriodicalId":18767,"journal":{"name":"Molecular Pharmacology","volume":"107 7","pages":"100053"},"PeriodicalIF":3.2000,"publicationDate":"2025-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.molpha.2025.100053","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
G protein-coupled receptors are known for their ability to generate a wide range of functional responses through interaction with various intracellular partners. This versatility is particularly evident within the chemokine receptor family, where conventional receptors signal primarily through classic G protein-coupled pathways while atypical chemokine receptors appear not to possess such ability but instead couple to alternative intracellular partners such as β-arrestins. Functional diversity in signaling presents unique opportunities for drug development, allowing different pathways to be selectively targeted to meet specific therapeutic needs. This minireview explores the mechanisms by which G protein-coupled receptor signaling, particularly within the chemokine receptor family, can be diversified at the modulatory, transmembrane, and intracellular levels. SIGNIFICANCE STATEMENT: This minireview explores how signaling in the chemokine receptor family diversifies at the ligand, transmembrane, and intracellular levels. This functional diversity presents unique opportunities for drug development by selectively targeting distinct pathways.
期刊介绍:
Molecular Pharmacology publishes findings derived from the application of innovative structural biology, biochemistry, biophysics, physiology, genetics, and molecular biology to basic pharmacological problems that provide mechanistic insights that are broadly important for the fields of pharmacology and toxicology. Relevant topics include:
Molecular Signaling / Mechanism of Drug Action
Chemical Biology / Drug Discovery
Structure of Drug-Receptor Complex
Systems Analysis of Drug Action
Drug Transport / Metabolism