Regeneron Pharmaceuticals, Inc., Tarrytown, New York.
Division of Endocrinology, Metabolism and Nutrition, Duke Molecular Physiology Institute, Duke University, Durham, North Carolina.
Endocrinology. 2018 Dec 1;159(12):4023-4032. doi: 10.1210/en.2018-00833.
The ghrelin-producing ε cell represents the fifth endocrine cell type in human pancreatic islets. The abundance of ε cells in adult pancreas is extremely low, which has hampered the investigation on the molecular pathways regulating the development and the function of this cell type. In this study, we explored the molecular features defining the function of pancreatic ε cells isolated from adult nondiabetic donors using single-cell RNA sequencing technology. We focus on transcription factors, cell surface receptors, and genes involved in metabolic pathways that contribute to regulation of cellular function. Furthermore, the genes that separate ε cells from the other islet endocrine cell types are presented. This study expands prior knowledge about the genes important for ε cell functioning during development and provides a resource to interrogate the transcriptome of this rare human islet cell type.
胃饥饿素产生细胞 ε 代表人类胰岛中的第五种内分泌细胞类型。成年胰腺中 ε 细胞的丰度极低,这阻碍了对调节该细胞类型发育和功能的分子途径的研究。在这项研究中,我们使用单细胞 RNA 测序技术探索了从成年非糖尿病供体中分离出的胰腺 ε 细胞的功能所定义的分子特征。我们专注于转录因子、细胞表面受体以及参与代谢途径的基因,这些基因有助于调节细胞功能。此外,还介绍了将 ε 细胞与其他胰岛内分泌细胞类型区分开来的基因。这项研究扩展了在发育过程中对与 ε 细胞功能相关的重要基因的认识,并为研究这种罕见的人类胰岛细胞类型的转录组提供了资源。