4.8 Article

Intrinsic Color Sensing System Allows for Real-Time Observable Functional Changes on Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes

Journal

ACS NANO
Volume 14, Issue 7, Pages 8232-8246

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c01745

Keywords

induced pluripotent stem cells; structural color; cardiac differentiation; microgroove; drug screening

Funding

  1. National Natural Science Fund of China [81670372]
  2. Shanghai Pujiang Program [18PJD031]
  3. Shanghai Collaborative Innovation Center for Translational Medicine [TM201821]
  4. National Key R&D Program of China [2019YFA0110400]
  5. Biomedical Engineering fund of Shanghai Jiao Tong University [YG2016MS28]
  6. pediatric postgraduate clinical research capacity improvement progress from School of Medicine, Shanghai Jiao Tong University [EKKY2018003DGD]
  7. Shanghai Key Laboratory of Tissue Engineering

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Stem-cell based in vitro differentiation for disease modeling offers great value to explore the molecular and functional underpinnings driving many types of cardiomyopathy and congenital heart diseases. Nevertheless, one major caveat in the application of in vitro differentiation of human induced pluripotent stem cell (hiPSC)-derived cardiomyocytes (hiPSC-CMs) involves the immature phenotype of the CMs. Most of the existing methods need complex apparatus and require laborious procedures in order to monitor the cardiac differentiation/maturation process and often result in cell death. Here we developed an intrinsic color sensing system utilizing a microgroove structural color methacrylated gelatin film, which allows us to monitor the cardiac differentiation process of hiPSC-derived cardiac progenitor cells in real time. Subsequently this system can be employed as an assay system to live monitor induced functional changes on hiPSC-CMs stemming from drug treatment, the effects of which are simply revealed through color diversity. Our research shows that early intervention of cardiac differentiation through simple physical cues can enhance cardiac differentiation and maturation to some extent. Our system also simplifies the previous complex experimental processes for evaluating the physiological effects of successful differentiation and drug treatment and lays a solid foundation for future transformational applications.

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