Advisor:  Robert E. Guldberg, School of Mechanical Engineering, Georgia Institute of Technology

Committee:
Ravi V. Bellamkonda, Department of Biomedical Engineering, Georgia Institute of Technology
Shawn R. Gilbert, School of Medicine, University of Alabama at Birmingham
W. Robert Taylor, School of Medicine, Emory University
Johnna S. Temenoff, Department of Biomedical Engineering, Georgia Institute of Technology

Severe extremity trauma often involves significant damage to multiple tissue types, including bones, skeletal muscles, peripheral nerves, and blood vessels.  Such injuries present unique challenges for reconstruction, and improving structural and functional outcomes of intervention remains a pressing, unmet clinical need.  While tissue engineering/regenerative medicine (TE/RM) therapeutics offer promising potential to overcome the status quo limitations of surgical reconstruction, very few products have transitioned to clinical practice.  Improving treatment options will likely require advancing our understanding of the biological interactions occurring in the repair of damaged tissues.

Bone tissue is known to be innervated and highly vascularized, and both tissue types are involved in normal bone physiology.  However, the degree to which these tissue relationships influence the repair of large, multi-tissue defects remains unknown.  Accordingly, the goal of this thesis was to investigate tissue regeneration in two novel composite injury models.  First, we characterized healing in a composite bone and nerve injury model where a segmental bone defect was combined with a peripheral nerve gap.  Our results indicated that although tissue regeneration was not impaired, the composite injury group experienced a marked functional deficit in the operated limb compared to single-tissue injury.  Second, we developed a model of composite bone and vascular extremity trauma by combining a critically-sized segmental bone defect with surgically-induced hind limb ischemia to evaluate the effects on BMP-2-mediated bone repair.  Interestingly, our results demonstrated a stimulatory effect of the recovery response to ischemia on bone regeneration.  Finally, we investigated early vascular growth and gene expression as potential mechanisms coupling the response to ischemia with bone defect repair.  Although the response to ischemia promoted robust vascular growth in the thigh, it did not directly augment vascularization at the site of bone regeneration.  In addition, the stimulatory effects of ischemia on bone regeneration could not be explained by gene expression alone based on the genes and time points investigated.

Taken together, this thesis presents pioneering work on a new thrust of TE/RM research – tissue regeneration in models of composite injury.  This work has provided new insights on the complexity of composite tissue repair, specifically in regard to the relationship between vascular tissue growth and bone healing.  Going forward, successful leverage of models of composite tissue injuries will provide valuable test beds to screen new technologies, advance the understanding of tissue repair biology, and ultimately, may produce new therapeutic interventions for limb salvage and reconstruction that improve outcomes for extremity trauma patients.