Development of multifunctional systems to mimic complex tissue interface

The motivation behind developing the biomimetic cellular platform is that many physiological processes are complex and dynamic involving spatiotemporal regulation of physical, chemical, and electrical signals in the cellular microenvironment. Our goal is to use engineering approaches, biomaterials, and cell technologies to design versatile systems that can manipulate these cues. In doing so, the multifunctional systems can 1) mimic the natural physiologic processes to study tissue and organ development; 2) understand the synergistic effects as well as creating biases in signaling to drive cell behaviors; 3) maximize the therapeutic potential of cellular response to design better regenerative strategies; and 4) screen potential drug candidates and personalize medicine for treatments.

 

Organs-on-chips

Translating scientific discoveries from animal models for curing human diseases can be very challenging, especially in the areas of neurodegenerative diseases. Animal models often don’t fully recapture human conditions due to differences in physiology, anatomy, injury mechanism, and regenerative potential. Additionally, animal research can be costly and time-consuming. Our goal is to create neurovascular units consisted of multiple cell types with microfluidic techniques to recapitulate the native physiological microenvironment in the brain. The organ-on-chip system will help us understand the biological development, multi-cellular interaction, and disease modeling and provide important insights for screening of neurological drugs and treatments.

 

Cancer Engineering 
Cancer progression is not solely driven by genetic mutations within tumor cells, it is influenced by the complex interplay between cancer cells and their microenvironment such as the extracellular matrix (ECM). The biochemical composition and biomechanical state of ECM can facilitate tumor emergence, metastasis, and treatment resistance. Our lab is interested in re-creating various aspects of tumor microenvironment by using stiffness-gradient biomaterials and engineering approaches to improve personalized medicine. We are grateful to our collaborators at the University of Arizona Cancer Center.



 

 

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cell therapy