MIT Fluid Mechanics Lab – Prof. C. Forbes Dewey (pioneering laboratory integrating fluid dynamics, biomechanics, and computational modeling to study vascular endothelial function and nitric oxide signaling)

MIT Fluid Mechanics Lab – Prof. C. Forbes Dewey (pioneering laboratory integrating fluid dynamics, biomechanics, and computational modeling to study vascular endothelial function and nitric oxide signaling)
Challenge

Nitric oxide (NO) is a critical signaling molecule produced by endothelial cells in response to shear stress, regulating vascular tone, inflammation, and atherosclerosis progression. However, traditional models treated NO production as isolated biochemical events, failing to capture the full systems-level integration of fluid mechanical forces, receptor activation, signaling cascades, feedback regulation, and downstream effects. Experimental validation of any comprehensive predictive model remained limited, hindering accurate simulation of vascular health and disease.

How CytoSolve Helped

The Dewey Lab collaborated with CytoSolve to conduct peer-reviewed validation of CytoSolve’s computational nitric oxide production model. CytoSolve’s platform:

  • Integrated thousands of peer-reviewed molecular pathways governing shear-stress sensing, eNOS activation, NO diffusion, and feedback modulation.
  • Incorporated biomechanical inputs (e.g., laminar/turbulent flow parameters) into a dynamic, quantitative systems architecture.
  • Generated precise predictions of NO bioavailability under physiologically relevant flow conditions for direct experimental comparison.

Key Benefits Realized

  • Rigorous Peer-Reviewed Validation
    Achieved independent confirmation of the model’s predictive accuracy through alignment with Dewey Lab’s gold-standard flow-chamber experiments and in vivo data.
  • Revealed Integrated Mechanochemical Mechanisms
    Confirmed previously underappreciated feedback loops linking fluid shear, calcium signaling, and NO synthesis—bridging mechanics and biochemistry at systems scale.
  • High-Impact Publication
    Validation results were published in Biophysical Journal (Cell Press), establishing CytoSolve’s NO model as a reliable standard for vascular mechanobiology research.
  • Advanced Vascular Disease Modeling
    Enabled more accurate in-silico simulation of endothelial dysfunction in atherosclerosis, hypertension, and diabetes—guiding therapeutic hypothesis generation.

Outcome

MIT’s Fluid Mechanics Lab, in collaboration with CytoSolve, completed the first peer-reviewed validation of a comprehensive nitric oxide systems model, with findings published in Biophysical Journal (Cell Press). This milestone confirmed the model’s fidelity in capturing mechanobiological regulation of vascular function, elevating standards for computational vascular biology and providing researchers with a powerful, validated tool to explore endothelial health and disease. This collaboration exemplifies how CytoSolve’s infrastructure delivers peer-validated, mechanistically accurate systems architectures—bridging fluid dynamics and molecular biology to drive breakthroughs in cardiovascular and endothelial research.