Title :
Temporal and spatial control over soluble protein signaling for musculoskeletal tissue engineering
Author :
Murphy, William L.
Author_Institution :
Univ. of Wisconsin, Madison, WI, USA
Abstract :
Orthopedic tissue engineering strategies have developed rapidly in response to large and growing clinical needs. However, current clinical methods for replacement of natural tissue function have significant limitations, and pragmatic challenges have hindered clinical use of emerging tissue engineering approaches. In addition, current methods are not yet capable of achieving complex spatial and temporal regulation of soluble signaling (e.g. growth factor signaling), which may be required for complex, functional tissue regeneration. We have begun to develop a series of new medical devices, which are designed to temporally and spatially regulate growth factor and cytokine signaling during tissue regeneration. The initial goal of these studies is to regulate the behavior of multipotent stem cells, and to promote formation of clinically relevant tissue interfaces (e.g. bone-tendon interfaces). The ultimate goal is to further understand and recapitulate the complex processes that lead to functional musculoskeletal development and regeneration.
Keywords :
biological tissues; orthopaedics; proteins; tissue engineering; cytokine signaling; growth factor; musculoskeletal tissue engineering; orthopedic tissue engineering; soluble protein signaling; spatial control; temporal control; tissue regeneration; Bone and Bones; Cytokines; Growth Substances; Guided Tissue Regeneration; Humans; Kinetics; Ligaments, Articular; Middle Aged; Musculoskeletal Diseases; Musculoskeletal Physiological Processes; Patella; Proteins; Regeneration; Rotator Cuff; Signal Transduction; Tendons; Tissue Engineering; United States;
Conference_Titel :
Engineering in Medicine and Biology Society, 2009. EMBC 2009. Annual International Conference of the IEEE
Conference_Location :
Minneapolis, MN
Print_ISBN :
978-1-4244-3296-7
Electronic_ISBN :
1557-170X
DOI :
10.1109/IEMBS.2009.5334306