Localisation of the relaxin-family peptide 3 receptor to enteroendocrine cells of the intestine in RXFP3-Cre/tdTomato mice

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY Biochemical pharmacology Pub Date : 2025-02-01 DOI:10.1016/j.bcp.2024.116714
Linda J. Fothergill , Mitchell T. Ringuet , Lara M. Voglsanger , Wesley J.N. Plange , Leigh C. Walker , Leni R. Rivera , Andrew J. Lawrence , Andrew L. Gundlach , Shanti Diwakarla , John B. Furness , Craig M. Smith
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Abstract

The relaxin-family peptide 3 receptor (RXFP3) and its native ligand, relaxin-3, are expressed in specific populations of brain neurons, and research on this system has focused on its role in the central nervous system. However, some studies have indicated that relaxin-3 and RXFP3 are also expressed in peripheral organs, including the gut. In this study, we characterised the identity of RXFP3-expressing cells in the gastrointestinal tract, using RXFP3-Cre/tdTomato reporter mice. We identified RXFP3-tdTomato expression in neurons throughout the small and large intestine, in cells in the lamina propria of the colon, and in enteroendocrine cells in the small intestine. We characterised the frequency and phenotype of the RXFP3-tdTomato + enteroendocrine cells in both the duodenum and distal ileum and discovered that the reporter was expressed in populations of cells that co-express 5-hydroxytryptamine (5-HT), cholecystokinin (CCK), secretin, peptide YY (PYY), oxyntomodulin, neurotensin, ghrelin, or glucose-dependent insulinotropic polypeptide (GIP). Faithful co-expression of Cre and RXFP3 mRNA was confirmed in RXFP3-Cre mice using multiplex, fluorescence in situ hybridisation (via RNAscope™). Our results indicate that RXFP3 is expressed by the LIN, X, K, Onecut3, and EC enteroendocrine cell types. In light of the key physiological roles of these cells, this study highlights the potential for relaxin-3 signalling via RXFP3 in enteroendocrine cells to modulate digestion, metabolism, food intake, and inflammatory processes.

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弛缓素家族肽 3 受体在 RXFP3-Cre/tdTomato 小鼠肠道内分泌细胞中的定位。
弛缓素家族肽 3 受体(RXFP3)及其原生配体弛缓素-3 在特定的脑神经元群体中表达,对该系统的研究主要集中在其在中枢神经系统中的作用。然而,一些研究表明,弛缓素-3 和 RXFP3 也在包括肠道在内的外周器官中表达。在这项研究中,我们利用 RXFP3-Cre/tdTomato 报告小鼠鉴定了胃肠道中 RXFP3 表达细胞的特征。我们在整个小肠和大肠的神经元、结肠固有层细胞以及小肠的肠内分泌细胞中发现了 RXFP3-tdTomato 的表达。我们对十二指肠和回肠远端的 RXFP3-tdTomato + 肠内分泌细胞的频率和表型进行了鉴定,发现该报告基因在同时表达 5-羟色胺 (5-HT)、胆囊收缩素 (CCK)、胰泌素、肽 YY (PYY)、oxyntomodulin、神经营养素、胃泌素或葡萄糖依赖性促胰岛素多肽 (GIP) 的细胞群中表达。使用多重荧光原位杂交技术(通过 RNAscope™)证实了 Cre 和 RXFP3 mRNA 在 RXFP3-Cre 小鼠中的忠实共表达。我们的研究结果表明,RXFP3 在 LIN、X、K、Onecut3 和 EC 肠内分泌细胞类型中均有表达。鉴于这些细胞的关键生理作用,本研究强调了肠内分泌细胞中的松弛素-3 信号通过 RXFP3 调节消化、新陈代谢、食物摄入和炎症过程的潜力。
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来源期刊
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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