Disease Modeling and Phenotypic Drug Screening for Diabetic Cardiomyopathy using Human Induced Pluripotent Stem Cells

Faye Drawnel(Roche (Switzerland)), Stefano Boccardo(Roche (Switzerland)), Michael Prummer(Roche (Switzerland)), Frédéric Delobel(Roche (Switzerland)), Alexandra Graff(University of Basel), Michaël Weber(Roche (Switzerland)), Régine Gérard(Roche (Switzerland)), Laura Badi(Roche (Switzerland)), Tony Kam‐Thong(Roche (Switzerland)), Lei Bu(Massachusetts General Hospital), Xin Jiang(Massachusetts General Hospital), Jean-Christophe Hoflack(Roche (Switzerland)), Anna Kiialainen(Roche (Switzerland)), Elena Jeworutzki(Roche (Switzerland)), Natsuyo Aoyama(Cellular Dynamics International (United States)), Coby B. Carlson(Cellular Dynamics International (United States)), Mark Burcin(Roche (Switzerland)), Gianni Gromo(Roche (Switzerland)), Markus Boehringer(Roche (Switzerland)), Henning Stahlberg(University of Basel), Benjamin J. Hall(Roche (Switzerland)), Maria Chiara Magnone(Roche (Switzerland)), Kyle L. Kolaja(Cellular Dynamics International (United States)), Kenneth R. Chien(Harvard University), J. Bailly(Roche (Switzerland)), Roberto Iacone(Roche (Switzerland))
Cell Reports
October 30, 2014
Cited by 244Open Access
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Abstract

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.


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