Grants Funded
Grant applicants for the 2024 cycle requested a total of nearly $3 million dollars. The PSF Study Section Subcommittees of Basic & Translational Research and Clinical Research evaluated more than 100 grant applications on the following topics:
The PSF awarded research grants totaling over $650,000 dollars to support more than 20 plastic surgery research proposals.
ASPS/PSF leadership is committed to continuing to provide high levels of investigator-initiated research support to ensure that plastic surgeons have the needed research resources to be pioneers and innovators in advancing the practice of medicine.
Research Abstracts
Search The PSF database to have easy access to full-text grant abstracts from past PSF-funded research projects 2003 to present. All abstracts are the work of the Principal Investigators and were retrieved from their PSF grant applications. Several different filters may be applied to locate abstracts specific to a particular focus area or PSF funding mechanism.
Fabrication of a Chemotactic Smart Scaffold for Bone Regeneration
Akishige Hokugo
2011
University of California, Los Angeles
A major focus in the field of craniofacial surgery is the development of tissue-engineered bone with biomimetic functionality allowing for its translation to the clinical setting. One of the greatest goals is achieving complete bone regeneration even on a large-scale defect. One challenge is the difficulty associated with successfully engrafting a bioactive construct with significant metabolic, circulatory, oxygenic, and nutritional needs into a potentially hostile growth environment. Our approach to this challenge is engineering a “smart scaffold” that incorporates the osteoconductive properties of an apatite-coated scaffold, the osteogenic potential of huma mesenchymal stem cells (HMSCs), and the angiogenic effects of vascular endothelial growth factor (VEGF) to effectively create an in situ regenerative bioreactor with self-sustaining qualities ensuring cell survival and prolonged tissue regeneration. By engineering HMSCs that overexpress VEGF, hypoxia at the defect site can be mitigated and the chemotactic effects of VEGF can support the homing and attachment of HMSCs to the scaffold, boosting its osteogenic potential.
