诱导多能干细胞
表型
糖尿病性心肌病
心肌病
糖尿病
疾病
药物发现
干细胞
医学
表型筛选
临床表型
生物信息学
生物
癌症研究
内科学
心力衰竭
细胞生物学
内分泌学
遗传学
胚胎干细胞
基因
作者
Faye Drawnel,Stefano Boccardo,Michael Prummer,Frédéric Delobel,Alexandra Graff,Michaël Weber,Régine Gérard,Laura Badi,Tony Kam‐Thong,Lei Bu,Xin Jiang,Jean-Christophe Hoflack,Anna Kiialainen,Elena Jeworutzki,Natsuyo Aoyama,Coby B. Carlson,Mark Burcin,Gianni Gromo,Markus Boehringer,Henning Stahlberg
出处
期刊:Cell Reports
[Cell Press]
日期:2014-10-30
卷期号:9 (3): 810-820
被引量:234
标识
DOI:10.1016/j.celrep.2014.09.055
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.
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