Disease Modeling and Phenotypic Drug Screening for Diabetic Cardiomyopathy using Human Induced Pluripotent Stem Cells
Faye M. Drawnel,
Stefano Boccardo,
Michael Prummer,
Frédéric Delobel,
Alexandra Graff,
Michael Weber,
Régine Gérard,
Laura Badi,
Tony Kam-Thong,
Lei Bu,
Xin Jiang,
Jean-Christophe Hoflack,
Anna Kiialainen,
Elena Jeworutzki,
Natsuyo Aoyama,
Coby Carlson,
Mark Burcin,
Gianni Gromo,
Markus Boehringer,
Henning Stahlberg,
Benjamin J. Hall,
Maria Chiara Magnone,
Kyle Kolaja,
Kenneth R. Chien,
Jacques Bailly,
Roberto Iacone
Affiliations
Faye M. Drawnel
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Stefano Boccardo
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Michael Prummer
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Frédéric Delobel
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Alexandra Graff
Center for Cell Imaging and Nano Analytics, Biozentrum, Department for Biosystems Science and Engineering, University of Basel, 4058 Basel, Switzerland
Michael Weber
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Régine Gérard
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Laura Badi
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Tony Kam-Thong
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Lei Bu
The Cardiovascular Research Center, Richard B. Simches Research Center, Massachusetts General Hospital, Suite 3201, Boston, MA 02114, USA
Xin Jiang
The Cardiovascular Research Center, Richard B. Simches Research Center, Massachusetts General Hospital, Suite 3201, Boston, MA 02114, USA
Jean-Christophe Hoflack
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Anna Kiialainen
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Elena Jeworutzki
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Natsuyo Aoyama
Cellular Dynamics International, Madison, WI 53711, USA
Coby Carlson
Cellular Dynamics International, Madison, WI 53711, USA
Mark Burcin
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Gianni Gromo
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Markus Boehringer
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Henning Stahlberg
Center for Cell Imaging and Nano Analytics, Biozentrum, Department for Biosystems Science and Engineering, University of Basel, 4058 Basel, Switzerland
Benjamin J. Hall
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Maria Chiara Magnone
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Kyle Kolaja
Cellular Dynamics International, Madison, WI 53711, USA
Kenneth R. Chien
Departments of Cell and Molecular Biology and of Medicine Huddinge, Karolinska Institutet, 171 77 Stockholm, Sweden
Jacques Bailly
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Roberto Iacone
Roche Pharma Research & Early Development, Roche Innovation Center Basel, 4070 Basel, Switzerland
Diabetic cardiomyopathy is a complication of type 2 diabetes, with known contributions of lifestyle and genetics. We develop environmentally and genetically driven in vitro models of the condition using human-induced-pluripotent-stem-cell-derived cardiomyocytes. First, we mimic diabetic clinical chemistry to induce a phenotypic surrogate of diabetic cardiomyopathy, observing structural and functional disarray. Next, we consider genetic effects by deriving cardiomyocytes from two diabetic patients with variable disease progression. The cardiomyopathic phenotype is recapitulated in the patient-specific cells basally, with a severity dependent on their original clinical status. These models are incorporated into successive levels of a screening platform, identifying drugs that preserve cardiomyocyte phenotype in vitro during diabetic stress. In this work, we present a patient-specific induced pluripotent stem cell (iPSC) model of a complex metabolic condition, showing the power of this technique for discovery and testing of therapeutic strategies for a disease with ever-increasing clinical significance.