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Human iPSC-derived cardiomyocytes and tissue engineering strategies for disease modeling and drug screening

期刊

BIOTECHNOLOGY ADVANCES
卷 35, 期 1, 页码 77-94

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.biotechadv.2016.12.002

关键词

Induced pluripotent stem cells; Cardiac differentiation; Tissue engineering; Disease modeling; Drug screening

资金

  1. Wallace H. Coulter Foundation Translational Research Partnership Award
  2. Washington State Life Science Discovery Fund [LSDF 9749063]
  3. American Heart Association [AHA 13SDG14560076]
  4. NIH [1R21EB020132-01A1, RO1 HL117991, 2T32HL007312-36A1, 5T32EB001650-12]
  5. International Collaborative RD Program
  6. KIAT - MOTIE [N0000894]
  7. McEwen Centre for Regenerative Medicine
  8. Peter Munk Cardiac Centre
  9. Ontario Institute for Regenerative Medicine
  10. Ministry of Trade, Industry & Energy (MOTIE), Republic of Korea [N0000894] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Improved methodologies for modeling cardiac disease phenotypes and accurately screening the efficacy and toxicity of potential therapeutic compounds are actively being sought to advance drug development and improve disease modeling capabilities. To that end, much recent effort has been devoted to the development of novel engineered biomimetic cardiac tissue platforms that accurately recapitulate the structure and function of the human myocardium. Within the field of cardiac engineering, induced pluripotent stem cells (iPSCs) are an exciting tool that offer the potential to advance the current state of the art, as they are derived from somatic cells, enabling the development of personalized medical strategies and patient specific disease models. Here we review different aspects of iPSC-based cardiac engineering technologies. We highlight methods for producing iPSC-derived cardiomyocytes (iPSC-CMs) and discuss their application to compound efficacy/toxicity screening and in vitro modeling of prevalent cardiac diseases. Special attention is paid to the application of micro- and nano-engineering techniques for the development of novel iPSC-CM based platforms and their potential to advance current preclinical screening modalities. Published by Elsevier Inc.

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