TY - JOUR
T1 - Functional human beige adipocytes from induced pluripotent stem cells
AU - Guénantin, Anne Claire
AU - Briand, Nolwenn
AU - Capel, Emilie
AU - Dumont, Florent
AU - Morichon, Romain
AU - Provost, Claire
AU - Stillitano, Francesca
AU - Jeziorowska, Dorota
AU - Siffroi, Jean Pierre
AU - Hajjar, Roger J.
AU - Fève, Bruno
AU - Hulot, Jean Sébastien
AU - Collas, Philippe
AU - Capeau, Jacqueline
AU - Vigouroux, Corinne
N1 - Publisher Copyright:
© 2017 by the American Diabetes Association.
PY - 2017/6/1
Y1 - 2017/6/1
N2 - Activation of thermogenic beige adipocytes has recently emerged as a promising therapeutic target in obesity and diabetes. Relevant human models for beige adipocyte differentiation are essential to implement such therapeutic strategies. We report a straightforward and efficient protocol to generate functional human beige adipocytes from human induced pluripotent stem cells (hiPSCs). Without overexpression of exogenous adipogenic genes, ourmethod recapitulates an adipogenic developmental pathway through successive mesodermal and adipogenic progenitor stages. hiPSC-derived adipocytes are insulin sensitive and display beige-specific markers and functional properties, including upregulation of thermogenic genes, increased mitochondrial content, and increased oxygen consumption upon activation with cAMP analogs. Engraftment of hiPSCderived adipocytes in mice produces well-organized and vascularized adipose tissue, capable of β-adrenergic- responsive glucose uptake. Our model of human beige adipocyte development provides a new and scalable tool for disease modeling and therapeutic screening.
AB - Activation of thermogenic beige adipocytes has recently emerged as a promising therapeutic target in obesity and diabetes. Relevant human models for beige adipocyte differentiation are essential to implement such therapeutic strategies. We report a straightforward and efficient protocol to generate functional human beige adipocytes from human induced pluripotent stem cells (hiPSCs). Without overexpression of exogenous adipogenic genes, ourmethod recapitulates an adipogenic developmental pathway through successive mesodermal and adipogenic progenitor stages. hiPSC-derived adipocytes are insulin sensitive and display beige-specific markers and functional properties, including upregulation of thermogenic genes, increased mitochondrial content, and increased oxygen consumption upon activation with cAMP analogs. Engraftment of hiPSCderived adipocytes in mice produces well-organized and vascularized adipose tissue, capable of β-adrenergic- responsive glucose uptake. Our model of human beige adipocyte development provides a new and scalable tool for disease modeling and therapeutic screening.
UR - http://www.scopus.com/inward/record.url?scp=85017024578&partnerID=8YFLogxK
U2 - 10.2337/db16-1107
DO - 10.2337/db16-1107
M3 - Article
C2 - 28270520
AN - SCOPUS:85017024578
SN - 0012-1797
VL - 66
SP - 1470
EP - 1478
JO - Diabetes
JF - Diabetes
IS - 6
ER -