New Technologies for Directing and Analyzing Cell Response to Engineered 3D Environments
New Technologies for Directing and Analyzing Cell Response to Engineered 3D Environments
Date: 08/22/2007
Time: 11:00 am
Location: TBA
Speaker: Jennie B. Leach, University of Maryland, Baltimore City
Efforts to engineer complex tissue therapies will be dramatically improved by a detailed understanding of how cells interact with their dynamic 3D environments. The effect of 3D matrix properties on cell behavior is still a relatively unexplored research field; as such, we lack design rules for engineering biomaterial scaffolds that effectively instruct cell response. Our work focuses on developing a detailed toolbox to manipulate biomaterials and cellular response in order to (1) study cell-matrix interactions underlying disease and (2) engineer functional tissue replacement therapies. Recent areas of research include the development of new technologies for 3D cell patterning, tuning the physicochemical properties of hydrogel tissue scaffolds, and monitoring cell microenvironmental cues (e.g., oxygen concentration) within 3D biomaterials. In applications of these technologies, we are interested in understanding how the physical nature of a 3D scaffold impacts cell behavior. For example, invasive cellular processes, such as nerve regeneration and cancer metastasis, critically rely on cells to migrate through and remodel of their 3D environment. It is not well understood, however, how these processes are impacted by the density or porosity of the material surrounding the cells. Furthermore, how do matrix degradability and stiffness mediate this response? Are physical properties of the matrix complementary or secondary to the biochemical cues in the cellular environment? By examining how physical properties impact neural and tumor cell behavior, we aim to formulate innovative therapeutic strategies for treating neurodegenerative disease and cancer.