Back to Search Start Over

A method for the generation of human stem cell-derived alpha cells

Authors :
Quan Zhou
Maria Sörhede-Winzell
Douglas A. Melton
Shaimaa Hassoun
Jennifer H. R. Kenty
Aleksey V. Matveyenko
Matthew R. Brown
Caden D. Duffy
Adrian Veres
Björn Tyrberg
Patrik Rorsman
Michael Q. Slama
Lihua Chen
Quinn P. Peterson
Haiqiang Dou
Source :
Nature Communications, Vol 11, Iss 1, Pp 1-14 (2020), Nature Communications
Publication Year :
2020
Publisher :
Nature Portfolio, 2020.

Abstract

The generation of pancreatic cell types from renewable cell sources holds promise for cell replacement therapies for diabetes. Although most effort has focused on generating pancreatic beta cells, considerable evidence indicates that glucagon secreting alpha cells are critically involved in disease progression and proper glucose control. Here we report on the generation of stem cell-derived human pancreatic alpha (SC-alpha) cells from pluripotent stem cells via a transient pre-alpha cell intermediate. These pre-alpha cells exhibit a transcriptional profile similar to mature alpha cells and although they produce proinsulin protein, they do not secrete significant amounts of processed insulin. Compound screening identified a protein kinase c activator that promotes maturation of pre-alpha cells into SC-alpha cells. The resulting SC-alpha cells do not express insulin, share an ultrastructure similar to cadaveric alpha cells, express and secrete glucagon in response to glucose and some glucagon secretagogues, and elevate blood glucose upon transplantation in mice.<br />Deriving functional pancreatic cell types from human stem cells may have important clinical applications. Building on previous work, here the authors generate stem cell-derived alpha cells via a polyhormonal intermediate, which have a gene expression pattern similar to human islet alpha cells and behave as such when transplanted into mice.

Details

Language :
English
ISSN :
20411723
Volume :
11
Issue :
1
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....1830555d671cc5d40102c6a337558a27