Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Maurice Wilkins Centre for Molecular Biodiscovery, New Zealand.
Biosci Rep. 2023 Apr 26;43(4). doi: 10.1042/BSR20221956.
RXFP4 is a G protein-coupled receptor (GPCR) in the relaxin family. It has recently been recognised that this receptor and its cognate ligand INSL5 may have a role in the regulation of food intake, gut motility, and other functions relevant to metabolic health and disease. Recent data from reporter-mice showed co-location of Rxfp4 and serotonin (5-HT) in the lower gut. We used human single-cell RNA sequence data (scRNASeq) to show that RXFP4 is in a subset of gut enterochromaffin cells that produce 5-HT in humans. We also used RNAScope to show co-location of Rxfp4 mRNA and 5-HT in mouse colon, confirming prior findings. To understand whether RXFP4 might regulate serotonin production, we developed a cell model using Colo320, a human gut-derived immortalised cell line that produces and releases serotonin. Overexpression of RXFP4 in these cells resulted in a constitutive decrease in cAMP levels in both the basal state and in cells treated with forskolin. Treatment of cells with two RXFP4 agonists, INSL5 derived peptide INSL5-A13 and small molecule compound-4, further reduced cAMP levels. This was paralleled by a reduction in expression of mRNA for TPH1, the enzyme controlling the rate limiting step in the production of serotonin. Overexpression of RXFP4 also attenuated the cAMP-induced release of serotonin from Colo320 cells. Together this demonstrates that serotonin producing enterochromaffin cells are the major site of RXFP4 expression in the gut and that RXFP4 can have inhibitory functional impacts on cAMP production as well as TPH1 expression and serotonin release.
RXFP4 是松弛素家族中的一种 G 蛋白偶联受体(GPCR)。最近人们认识到,该受体及其同源配体 INSL5 可能在调节食物摄入、肠道蠕动和其他与代谢健康和疾病相关的功能方面发挥作用。来自报告基因小鼠的数据显示,Rxfp4 与血清素(5-HT)在下肠道中共同定位。我们使用人类单细胞 RNA 序列数据(scRNASeq)表明,RXFP4 存在于人类肠道嗜铬细胞的一个亚群中,这些细胞产生 5-HT。我们还使用 RNAScope 显示了 Rxfp4 mRNA 和 5-HT 在小鼠结肠中的共定位,证实了先前的发现。为了了解 RXFP4 是否可能调节 5-HT 的产生,我们使用 Colo320 开发了一种细胞模型,Colo320 是一种源自人类肠道的永生化细胞系,可产生和释放 5-HT。在这些细胞中过表达 RXFP4 会导致 cAMP 水平在基础状态和用 forskolin 处理的细胞中持续下降。用两种 RXFP4 激动剂,即 INSL5 衍生肽 INSL5-A13 和小分子化合物 4 处理细胞,进一步降低了 cAMP 水平。这与控制 5-HT 产生的限速步骤的酶 TPH1 的 mRNA 表达减少平行。过表达 RXFP4 还减弱了 Colo320 细胞中 cAMP 诱导的 5-HT 释放。综上所述,这表明肠道中产生 5-HT 的嗜铬细胞是 RXFP4 表达的主要部位,并且 RXFP4 可以对 cAMP 产生以及 TPH1 表达和 5-HT 释放产生抑制性功能影响。