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.
Real time fate mapping of palatogenic cranial neural crest cells
Eric Chien-Wei Liao MD, PhD
2010
Massachusetts General Hospital (The General Hospital Corp.)
Pilot Research Grant
Cranio / Maxillofacial / Head and Neck, Other
Palatogenesis involves complex cellular movement and morphogenesis events that are difficult to study in a mammalian model. The zebrafish (Danio rerio) is a powerful model for studying palate development owing to its developmental, genetic, and practical characteristics. Several studies have established that the zebrafish embryonic ethmoid plate is analogous to mammalian
palate structure. Zebrafish embryos develop ex vivo and are transparent, where migratory neural crest cells can be fate-mapped in real time. Lineage-specific labeling of migrating neural crest cells could be achieved by generating a transgenic fish where the sox10 promoter drives the expression of the green-to-red photoconvertable protein, kaede. Endogenous sox10 gene expression is restricted to neural crest cells, oligodendrocytes, and the otic epithelium. Therefore, the
sox10:kaede transgenic will provide a powerful method of following neural crest cells migrating to form the face at single-cell resolution, in real time. Our first specific aim is to generate a sox10::kaede transgenic zebrafish.
Our second specific aim is to use sox10::kaede to trace neural crest cell lineage in the context of gene knockdown and mutant zebrafish. The results of these lineage tracing experiments will be compared to previous work on zebrafish neural crest migration, to improve our
understanding of this intricate process. In addition to being well suited for genetic manipulations, zebrafish have also been used to successfully identify chemical modifiers of vascular and hematopoietic phenotypes.
Our third aim is to dissect the Wnt regulatory pathway in zebrafish oropharyngeal
development, with functional and biochemical analysis of Wnt9a. Wnt signaling provides important
cues regulating migration of neural crest cells that form the vertebrate craniofacial structures. We are exploiting the advantages of the zebrafish system to elucidate the role of Wnt signaling in palatogenesis, through morphogenetic studies of Wnt9a.
