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

被引:203
作者
Drawnel, Faye M. [1 ]
Boccardo, Stefano [1 ,2 ]
Prummer, Michael [1 ]
Delobel, Frederic [1 ]
Graff, Alexandra [3 ]
Weber, Michael [1 ]
Gerard, Regine [1 ]
Badi, Laura [1 ]
Kam-Thong, Tony [1 ]
Bu, Lei [4 ]
Jiang, Xin [4 ]
Hoflack, Jean-Christophe [1 ]
Kiialainen, Anna [1 ]
Jeworutzki, Elena [1 ]
Aoyama, Natsuyo [5 ]
Carlson, Coby [5 ]
Burcin, Mark [1 ]
Gromo, Gianni [1 ]
Boehringer, Markus [1 ]
Stahlberg, Henning [3 ]
Hall, Benjamin J. [1 ]
Magnone, Maria Chiara [1 ]
Kolaja, Kyle [5 ]
Chien, Kenneth R. [6 ,7 ,8 ]
Bailly, Jacques [1 ]
Iacone, Roberto [1 ]
机构
[1] Roche Innovat Ctr Basel, Roche Pharma Res Early Dev, CH-4070 Basel, Switzerland
[2] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[3] Univ Basel, Biozentrum, Dept Biosystems Sci & Engn, Ctr Cell Imaging & Nano Analyt, CH-4058 Basel, Switzerland
[4] Massachusetts Gen Hosp, Richard B Simches Res Ctr, Cardiovasc Res Ctr, Boston, MA 02114 USA
[5] Cellular Dynam Int, Madison, WI 53711 USA
[6] Karolinska Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden
[7] Karolinska Inst, Dept Med Huddinge, S-17177 Stockholm, Sweden
[8] Harvard Univ, Harvard Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
关键词
DIFFERENTIATION; STRESS;
D O I
10.1016/j.celrep.2014.09.055
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:810 / 820
页数:11
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