• DocumentCode
    636672
  • Title

    2D data-driven stalk cell prediction model based on tip-stalk cell interaction in angiogenesis

  • Author

    Mengmeng Wang ; Ong, Lee-Ling S. ; Dauwels, Justin ; Asada, H. Harry

  • Author_Institution
    Sch. of Electr. & Electron. Eng., Nanyang Technol. Univ., Singapore, Singapore
  • fYear
    2013
  • fDate
    3-7 July 2013
  • Firstpage
    4537
  • Lastpage
    4540
  • Abstract
    Angiogenesis is the growth process of blood vessels from existing vessels. During angiogenesis, endothelial cells (ECs), which line the vessel, specialize into tip and stalk cells. Tip cells respond to angiogenic signals, burrow into the extracellular matrix (ECM) and form conduits. Stalk cells follow the tip cells along the conduits, and form solid sprouts or lumen vessels. Interactions between stalk cells and tip cells are important for creating functional vessels. The goal of this work is to predict stalk cells migration trajectories from known tip cell trajectories. Four factors influence the position and velocity of cell migration in ECM: cell-cell interaction, drag force, chemotactic signal and cell-ECM interaction. As chemotactic signal and cell-ECM interactions have little effect on stalk cell movement, the proposed model includes the influence of cell-cell interactions and drag force only. The unknown parameters in the model are inferred by Maximum Likelihood Estimation (MLE) from experimental time-lapse cell migration data. Numerical results suggest that the proposed model can accurately predict stalk cell trajectories. The proposed model may be useful for the study of angiogenesis, a critical process for cancer tumor growth.
  • Keywords
    biomechanics; cell motility; drag; maximum likelihood estimation; numerical analysis; physiological models; angiogenesis; blood vessel; cancer tumor growth; cell-ECM interaction; chemotactic signal; drag force; endothelial cell; extracellular matrix; lumen vessel; maximum likelihood estimation; stalk cell migration trajectory; stalk cell movement; stalk cell prediction model; time-lapse cell migration 2D data; tip-stalk cell interaction; Computational modeling; Drag; Electronic countermeasures; Force; Mathematical model; Predictive models; Trajectory;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Engineering in Medicine and Biology Society (EMBC), 2013 35th Annual International Conference of the IEEE
  • Conference_Location
    Osaka
  • ISSN
    1557-170X
  • Type

    conf

  • DOI
    10.1109/EMBC.2013.6610556
  • Filename
    6610556