I am interested in engineering multicellular tissue models that combine biologically relevant complexity with precise experimental control. By integrating biomaterials with three-dimensional and perfusable culture systems, these platforms can provide opportunities to investigate how extracellular matrix properties influence vascular organization, immune cell behavior, and communication among cell populations.
Focuses: vascularization • inflammation • immune-vascular interactions • microphysiological systems
Disease progression is accompanied by evolving changes in extracellular matrix composition, mechanics, and architecture that influence interactions among multiple cell populations. My future research will explore how dynamic tissue microenvironments contribute to cellular dysfunction and disease progression, with particular interest in neurovascular biology and neurodegenerative disease. Engineered human tissue models offer opportunities to investigate these relationships under experimentally controlled conditions.
Focuses: ECM remodeling • disease progression • tissue dysfunction • microenvironmental history
My research will explore how natural, synthetic, and hybrid biomaterials can be engineered to reproduce essential features of native tissue microenvironments while maintaining experimental control. By integrating biological insights with materials design, I aim to identify which biochemical, mechanical, and architectural properties are most important for supporting tissue-specific function and develop adaptable materials strategies for engineering physiologically relevant tissues.
Focuses: natural/synthetic/hybrid biomaterials • tissue-specific ECM • spatial organization • biology-driven material design
My research spans biomaterials design, vascular tissue engineering, and the development of experimentally controlled tissue models. Building on established work in vascularization and dynamic biomaterials, I am interested in extending these approaches to investigate immune-vascular interactions, disease-associated microenvironmental remodeling, and tissue-specific function. These directions offer opportunities to connect fundamental materials engineering with mechanistic biological discovery across diverse tissues and disease contexts.