4.4 Article

The orphan MRGPRF receptor is expressed in entero-endocrine cells of the human gut mucosa

期刊

CELL AND TISSUE RESEARCH
卷 393, 期 2, 页码 393-399

出版社

SPRINGER
DOI: 10.1007/s00441-023-03797-z

关键词

Mas-related G protein-coupled receptor; MRGPR; Intestine; Mucosa; Enteroendocrine cell

向作者/读者索取更多资源

In recent years, it has been discovered that the family of Mas-related G protein-coupled receptors (MRGPRs) plays a crucial role in neuro-immune communication in the skin. However, the expression of MRGPRs at other mucosal surfaces remains poorly understood. This study aimed to investigate the expression of MRGPRs in mucosal biopsies of the human gastrointestinal (GI) tract. The results showed that MRGPRF mRNA was the only detectable member of the MRGPR family expressed in human mucosal biopsies of the terminal ileum and sigmoid colon. Immunohistochemical analysis revealed that MRGPRF was specifically expressed in mucosal entero-endocrine cells (EECs).
In the past years, it has become clear that the family of Mas-related G protein-coupled receptors plays a central role in neuro-immune communication at mucosal barrier surfaces, in particular in the skin. Remarkably, MRGPR expression at other mucosal surfaces remains poorly characterized. To fill this gap in our understanding, the present study was undertaken to screen and verify the expression of the human MRGPR family members in the mucosal biopsies of the human gastrointestinal (GI) tract. Our findings revealed that, of all human MRGPRs family members, only MRGPRF mRNA is expressed at detectable levels in human mucosal biopsies of both terminal ileum and sigmoid colon. Furthermore, immunohistochemical stainings revealed that MRGPRF is specifically expressed by mucosal entero-endocrine cells (EECs). Overall, this study showed for the first time that the human ileum and colonic mucosa represent a novel expression site for the orphan MRGPRF, more specifically in EECs.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据