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.
Enhancement of Wound Healing through Autologous CRISPR/Cas-edited Dendritic Cells
Dominic Henn MD
2019
Stanford University
Translational and Innovation Research Grant
Wounds / Scar
The goal of our project is to develop a novel therapeutic approach to facilitate healing of chronic wounds, e.g. in patients with diabetes or atherosclerotic vascular disease by isolating an individual's own dendritic cells (DCs) and reapplying them to the wound bed after CRISPR/Cas9 gene editing (adoptive cell transfer, ACT). The target gene to be modified in its expression is the N-Myc downstream-regulated gene 2 (NDRG2), which is highly expressed in DCs and controls the growth of several human tissues, including blood vessels, by inhibiting cell proliferation and enhancing apoptosis. We hypothesize that targeted knockout of NDRG2 in DCs promotes angiogenesis and facilitates wound healing. To test this hypothesis, we will establish a co-culture system of human umbilical vein endothelial cells (HUVECs) and activated monocyte-derived DCs to determine the effect of NDRG2 knockout resp. drug-induced down-regulation in DCs on endothelial cell behavior in vitro (Specific Aim #1). Moreover, we will investigate whether ex vivo knockout of NDRG2 in DCs by means of CRISPR/Cas9 facilitates wound healing in diabetic and non-diabetic mouse full-thickness excisional wound models. Our long-term objective is to transfer the acquired knowledge into more complex models of large mammals and, as an ultimate goal, to develop clinically applicable tools to save patients with impaired wound healing from amputations.
