Gene Signature of the Human Pancreatic ε Cell
Author(s) -
Giselle Domínguez Gutiérrez,
Jinrang Kim,
Ann–Hwee Lee,
Jenny Tong,
Jingjing Niu,
Sarah M. Gray,
Yi Wei,
Yueming Ding,
Min Ni,
Christina Adler,
Andrew Murphy,
Jesper Gromada,
Yurong Xin
Publication year - 2018
Publication title -
endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.674
H-Index - 257
eISSN - 1945-7170
pISSN - 0013-7227
DOI - 10.1210/en.2018-00833
Subject(s) - biology , enteroendocrine cell , islet , pancreas , transcriptome , cell type , cell , gene , pax4 , pancreatic islets , microbiology and biotechnology , endocrine system , receptor , endocrinology , function (biology) , medicine , transcription factor , gene expression , genetics , insulin , hormone , homeobox
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.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom