Galie Lab
Galie Lab
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    • Home
    • Research
    • Lab Members
    • Outreach
    • Contact
  • Home
  • Research
  • Lab Members
  • Outreach
  • Contact

Research

Our laboratory interrogates how mechanical and biochemical factors influence cell-matrix crosstalk and develops biomaterial-based therapeutic strategies that exploit this interaction. 



Our list of publications can be found here: 

Our Areas of Interest

Blood-Brain Barrier Response to Shear Stress

Blood-Brain Barrier Response to Shear Stress

Blood-Brain Barrier Response to Shear Stress

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Biomaterials for Tissue Regeneration

Blood-Brain Barrier Response to Shear Stress

Blood-Brain Barrier Response to Shear Stress

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Synthetic Mechanobiology

Blood-Brain Barrier Response to Shear Stress

Synthetic Mechanobiology

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Studying the effect of fluid flow on the blood-brain barrier

Putting the "blood" in blood-brain barrier

Our laboratory has developed several models that mimic different levels of brain blood vessel architecture spanning from capillary to artery scale. We use these models, which can be exposed to varying levels of fluid flow rate and pressures, to study how changes in blood flow affect the integrity of the blood-brain barrier, a term for decreased transport across blood vessels in the brain and spinal cord. Recently, we have begun to incorporate whole blood flow in 3D-printed models to better mimic the environment inside the body. We use techniques that include microparticle image velocimetry (microPIV) to characterize the blood flow and determine its effects on blood-endothelial interactions. We are also developing novel drag-reducing polymers to alter hemodynamics within 3D-printed vasculature.

Novel biomaterials for central nervous system regeneration

Biomaterial scaffolds for spinal cord injury repair

The injury environment after spinal cord injury is dynamic and complex, with multiple cell types and cytokines, which motivates our approach to create tunable, multifunctional biomaterials to combat processes that exacerbate the damage from an initial insult. These injectable materials have the ability to deliver a combination of different classes of therapeutics (e.g., small molecules, peptides, and monoclonal antibodies) to the injury site. In collaboration with Dr. Itzhak Fischer and Dr. Ying Jin at Drexel University, we are studying how these materials improve functional recovery of the spinal cord after injury. The overall goal of this work is to determine the combination of cargo that best improves tissue regeneration. Although our current work focuses on the spinal cord, this platform is broadly applicable to different tissues and injury environments.

Reprogramming cells to alter mechanotransductive signaling

Development and application of synthetic post-translational circuits

Our laboratory has contributed to the development of a novel post-translational circuit, coupling synthetic phosphorylation networks with split fluorescent and luminescent proteins, denoted as SPN-FLUX (synthetic phosphorylation networks with fluorescence and luminescence expansion). This platform provides an avenue isolated from native kinetics by which inducible protein-protein interactions are utilized to study cells’ interactions with their environment. We propose to use these inducible protein interactions to dictate response to mechanical forces applied to the matrix, with the goal of creating synthetic cells that have therapeutic potential in pathologies characterized by changes in tissue mechanics.

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