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Gene Signature of Proliferating Human Pancreatic α Cells
Author(s) -
Giselle Domínguez Gutiérrez,
Yurong Xin,
Haruka Okamoto,
Jinrang Kim,
Ann–Hwee Lee,
Min Ni,
Christina Adler,
George D. Yancopoulos,
Andrew Murphy,
Jesper Gromada
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.2018-00469
Subject(s) - cell cycle , biology , cell growth , cell , cell division , proliferating cell nuclear antigen , microbiology and biotechnology , gene , gene expression , cellular differentiation , genetics
Pancreatic α cells proliferate at a low rate, and little is known about the control of this process. Here we report the characterization of human α cells by large-scale, single-cell RNA sequencing coupled with pseudotime ordering. We identified two large subpopulations and a smaller cluster of proliferating α cells with increased expression of genes involved in cell-cycle regulation. The proliferating α cells were differentiated, had normal levels of GCG expression, and showed no signs of cellular stress. Proliferating α cells were detected in both the G1S and G2M phases of the cell cycle. Human α cells proliferate at a fivefold higher rate than human β cells and express lower levels of the cell-cycle inhibitors CDKN1A and CDKN1C. Collectively, this study provides the gene signatures of human α cells and the genes involved in their cell division. The lower expression of two cell-cycle inhibitors in human α cells could account for their higher rate of proliferation compared with their insulin-producing counterparts.

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