• DocumentCode
    346801
  • Title

    Three-dimensional environment promotes in vitro differentiation of cardiac myocytes

  • Author

    Bursac, N. ; Papadaki, M. ; Langer, R. ; Eisenberg, S.R. ; Vunjak-Novakovic, G. ; Freed, L.E.

  • Author_Institution
    Div. of Health Sci. & Technol., MIT, Cambridge, MA, USA
  • Volume
    1
  • fYear
    1999
  • fDate
    1999
  • Abstract
    Previous studies demonstrated that three-dimensional (3D) engineered cardiac muscle tissue can be created in vitro with structural and functional properties resembling those of native cardiac muscle. In this study, the authors investigated the effect of 3D vs. two-dimensional (2D) culture environment on cell differentiation. Primary ventricular cardiac muscle cells were cultivated in a 3D (on fibrous polymer scaffolds to form an engineered cardiac muscle) or a 2D culture system (in Petri dishes to form confluent cell monolayers) under otherwise identical conditions. Cell size was similar for 2D and 3D cultures. The amounts of gap junctional protein connexin-43 (an index of electrical coupling) and creatine kinase-MM (differentiation marker) were significantly higher in 3D than in 2D cultures, suggesting that the 3D environment promoted cell differentiation, probably due to increased cell-cell communication and more physiological cell shape. Similar trends were observed for tissue electrophysiological properties, where it was shown that in contrast to 2D cultures, cardiac myocytes in 3D cultures did not beat spontaneously but were readily excitable
  • Keywords
    bioelectric phenomena; cardiology; cellular biophysics; monolayers; muscle; proteins; Petri dishes; cardiac myocytes; confluent cell monolayers; electrical coupling index; fibrous polymer scaffolds; gap junctional protein connexin-43; in vitro differentiation promotion; native cardiac muscle; primary ventricular cardiac muscle cells; three-dimensional environment; tissue electrophysiological properties; Chemical engineering; Chemical technology; Couplings; In vitro; Muscles; Pediatrics; Physiology; Polymers; Protein engineering; Shape;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    [Engineering in Medicine and Biology, 1999. 21st Annual Conference and the 1999 Annual Fall Meetring of the Biomedical Engineering Society] BMES/EMBS Conference, 1999. Proceedings of the First Joint
  • Conference_Location
    Atlanta, GA
  • ISSN
    1094-687X
  • Print_ISBN
    0-7803-5674-8
  • Type

    conf

  • DOI
    10.1109/IEMBS.1999.802169
  • Filename
    802169