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A method for the generation of human stem cell-derived alpha cells.
Peterson, Quinn P; Veres, Adrian; Chen, Lihua; Slama, Michael Q; Kenty, Jennifer H R; Hassoun, Shaimaa; Brown, Matthew R; Dou, Haiqiang; Duffy, Caden D; Zhou, Quan; Matveyenko, Aleksey V; Tyrberg, Björn; Sörhede-Winzell, Maria; Rorsman, Patrik; Melton, Douglas A.
Afiliação
  • Peterson QP; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA. peterson.quinn@mayo.edu.
  • Veres A; Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, USA. peterson.quinn@mayo.edu.
  • Chen L; Center for Regenerative Medicine, Mayo Clinic, Rochester, MN, USA. peterson.quinn@mayo.edu.
  • Slama MQ; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
  • Kenty JHR; Cardiovascular, Renal and Metabolism and Early Development, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Hassoun S; Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, USA.
  • Brown MR; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
  • Dou H; Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, USA.
  • Duffy CD; Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, USA.
  • Zhou Q; Department of Physiology, University of Gothenburg, Gothenburg, Sweden.
  • Matveyenko AV; Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, USA.
  • Tyrberg B; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
  • Sörhede-Winzell M; Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, USA.
  • Rorsman P; Cardiovascular, Renal and Metabolism and Early Development, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Melton DA; Department of Physiology, University of Gothenburg, Gothenburg, Sweden.
Nat Commun ; 11(1): 2241, 2020 05 07.
Article em En | MEDLINE | ID: mdl-32382023
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnicas de Cultura de Células / Células-Tronco Pluripotentes / Células Secretoras de Glucagon / Células Secretoras de Insulina Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnicas de Cultura de Células / Células-Tronco Pluripotentes / Células Secretoras de Glucagon / Células Secretoras de Insulina Idioma: En Ano de publicação: 2020 Tipo de documento: Article