Sensor extended imaging workflow for creating fit for purpose models in basic and applied cell biology.

Julia Schueler, Heikki Sjöman, Carlo Kriesi
Author Information
  1. Julia Schueler: Charles River Germany GmbH, Am Flughafen 12-14, 79111, Freiburg, Germany. julia.schueler@crl.com. ORCID
  2. Heikki Sjöman: Vitroscope AS, Leirfossvegen 5d, 7037, Trondheim, Norway. ORCID
  3. Carlo Kriesi: Vitroscope AS, Leirfossvegen 5d, 7037, Trondheim, Norway. ORCID

Abstract

While various engineering disciplines spent years on developing methods and workflows to increase their R&D efficiency, the field of cell biology has seen limited evolution in the fundamental approaches to interact with living cells. Perturbations are mostly of chemical nature, and physiologically relevant contexts and stimuli are left with limited attention, resulting in a solution space constrained within the boundaries of presently manageable perturbations. To predict in the laboratory how a drug will work in a human patient, cell biology must have a closer look at life and strive to mimic the human being in all his complexity. By implementing an iterative process from perturbation to measurement and vice versa, the authors suggest using a sensor-extended imaging workflow to implement product development practices to cell biology, opening a physiologically relevant solution space for the development of truly translational and predictive fit for purpose in vitro cell models.

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MeSH Term

Humans
Software
Workflow
Diagnostic Imaging

Word Cloud

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