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Induction of cardiomyocyte-like cells from hair follicle cells in mice

  • Yong-Hee Kim (Department of Animal Science and Technology, College of Biotechnology and Natural Resources, Chung-Ang University) ;
  • Bang-Jin Kim (Department of Cancer Biology, Perelman School of Medicine at the University of Pennsylvania) ;
  • Seok-Man Kim (Department of Animal Science and Technology, College of Biotechnology and Natural Resources, Chung-Ang University) ;
  • Sun-Uk Kim (National Primate Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Buom-Yong Ryu (Department of Animal Science and Technology, College of Biotechnology and Natural Resources, Chung-Ang University)
  • Received : 2018.07.16
  • Accepted : 2019.03.08
  • Published : 20190500

Abstract

Hair follicles (HFs) are a well-characterized niche for adult stem cells (SCs), and include epithelial and melanocytic SCs. HF cells are an accessible source of multipotent adult SCs for the generation of the interfollicular epidermis, HF structures and sebaceous glands in addition to the reconstitution of novel HFs in vivo. In the present study, it was demonstrated that HF cells are able to be induced to differentiate into cardiomyocyte-like cells in vitro under specific conditions. It was determined that HF cells cultured on OP9 feeder cells in KnockOut-Dulbecco's modified Eagle's medium/B27 in the presence of vascular endothelial growth factors differentiated into cardiomyocyte-like cells that express markers specific to cardiac lineage, but do not express non-cardiac lineage markers including neural stem/progenitor cell, HF bulge cells or undifferentiated spermatogonia markers. These cardiomyocyte-like cells exhibited a spindle- and filament-shaped morphology similar to that presented by cardiac muscles and exhibited spontaneous beating that persisted for over 3 months. These results demonstrate that SC reprogramming and differentiation may be induced without resulting in any genetic modification, which is important for the clinical applications of SCs including tissue and organ regeneration.

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Acknowledgement

The present study was supported by the Bio and Medical Technology Development Program of the National Research Foundation of Korea (NRF) funded by the Korean government, MSIT (grant no. 2018M3A9H1023139), the Basic Science Research Program through the NRF funded by the Ministry of Education (grant no. 2018R1A6A1A03025159) and the Korea Research Institute of Bioscience and Biotechnology Research Initiative Programs (grant no. KGM4251824).