*********************************
There is now a CONTENT FREEZE for Mercury while we switch to a new platform. It began on Friday, March 10 at 6pm and will end on Wednesday, March 15 at noon. No new content can be created during this time, but all material in the system as of the beginning of the freeze will be migrated to the new platform, including users and groups. Functionally the new site is identical to the old one. webteam@gatech.edu
*********************************
"Systems Tissue Engineering"
Lonnie D. Shea, PhD
Professor
Chemical & Biological Engineering
Northwestern University
Systems and strategies for promoting tissue growth provide enabling technologies for either enhancing regeneration for diseased or injured tissues, or to investigate abnormal tissue formation such as cancer. Given the complexity inherent in tissues, my laboratory is working towards the concept of "Systems Tissue Engineering", which indicates the dual need i) to develop systems capable of presenting combinations of factors that drive tissue growth, as well as ii) to incorporate systems biology approaches that can identify the appropriate combination of factors. Biomaterial scaffolds represent a central component of many approaches and provide the enabling tools for creating an environment and/or deliver factors that can direct cellular processes toward tissue formation. We have developed scaffolds with the objective of providing factors to stimulate growth and also blocking factors that inhibit regeneration, and will illustrate this approach through our work with islet transplantation in Type 1 Diabetes therapy and scaffolds for the early detection of cancer. The immune response has become a central focus, and will present results for local immunomodulation around the scaffold, as well as the development of nanoparticles for modulating the immune response, in order to induce tolerance in autoimmune disease and allogeneic cell transplantation. The ability to present multiple factors raises the challenge of identifying the combination that will maximally promote tissue formation. Toward this goal, we have developed a cellular array for the large scale profiling of transcription factor activity throughout tissue formation, which we propose can identify the factors necessary to drive cells towards the desired phenotype. This array represents a novel systems biology tool for molecularly dissecting tissue formation. This approach of relating tissue development to molecular design of the scaffold may ultimately lead to the formation of engineered tissues that could provide alternatives to whole organ or tissue transplantation.
Bob Guldberg, PhD - faculty host
