Plastic Surgery About Us Message from the Chair Contact Us Education & Training Visiting Medical Students Fellowship Programs Residency Program Research Center for Tissue Engineering (CTE) Faculty Research — Miles J. Pfaff Clinical Expertise Faculty Center for Tissue Engineering (CTE) Home About Campus & Community Resources Communications & Public Relations Office Plastic Surgery: Research > Center For Tissue Engineering (CTE) Innovative Solutions for Wound-Healing & Regenerative Medicine The Department of Plastic Surgery's Center for Tissue Engineering (CTE) focuses on creating innovative medical devices, investigating the causes and reversal of fibrosis, studying nuances in adipose stem cell behavior, developing oxygenated wound-healing solutions and developing cartilage frameworks. Adipose-derived stem cells serve as the central focus of the cellular work, with multiple projects emanating from this core. Projects All projects and protocols are designed with a translational bias with relatively low barriers to entry to the marketplace. In conjunction with our academic partners, mainly biomedical engineers, many projects involve the design of medical devices to serve these translational purposes. Fibrosis — Dupuytren’s disease Dupuytren’s disease is a fibroproliferative disorder that affects the palm, fingers and feet, causing a stiff, persistent flexion of the fingers due to the contraction of fibrous cords. The pathogenesis of Dupuytren’s contracture involves pathologic myofibroblasts in the palmar fascia that secrete abnormal collagens and induce contracture. CTE has investigated the use of PRP (platelet-rich plasma), adipose-derived stem cells, growth factors and small molecules to reprogram myofibroblasts into adipocyte-like cells, thereby converting scar tissue into fat tissue. Publications: Targeting Myofibroblasts as a Treatment Modality for Dupuytren Disease Transforming Myofibroblasts Into Lipid-Filled Cells to Treat Dupuytren Diseas GLP-1 Signaling The unpredictable nature of scarring after surgery challenges plastic surgeons and concerns patients' mental health. Glucagon-like Peptide-1 receptor agonists and Dipeptidyl Peptidase-4 inhibitors are anti-diabetic drugs that lower glucagon and raise insulin levels in Type II Diabetes Mellitus. We hypothesize that GLP-1 modulates fibrotic and adipogenic pathways in the skin to promote tissue regeneration. We are exploring how GLP-1 signaling affects dermal fibrosis and tissue repair. Publications: From Glucose to Gauze: A Systematic Review on the Various Wound Healing Properties of DPP-4 Inhibitors Beyond Glycaemic Control Glucagon-Like Peptide-1 Receptor Agonists: Friend or Foe of Aesthetic Medicine? Sclerosing Skin Disorders Sclerosing Skin Disorders, such as scleroderma, morphea and eosinophilic fasciitis, affect the skin and underlying connective tissues. Specific subsets of fibroblasts have been identified as drivers of these conditions, mainly myofibroblasts, which are characterized by the expression of -SMA (smooth muscle actin). However, the similarities and differences in molecular mechanisms among these fibrotic disorders remain unclear. In collaboration with the Department of Dermatology (Michelle Min, MD), we are exploring markers of skin fibrosis to explore these differences. Vascular Signaling Crosstalk between adipose-derived stem cells (ASCs) and endothelial cells promotes metabolic fitness and influences vessel growth. We are evaluating whether ASCs induce angiogenesis through a glycolytic mechanism. California Society of Plastic Surgeons 75th Annual Meeting — UC Irvine Center for Tissue Engineering Research Abstract:Enhancing Fat Graft Survival Through Adipose-Derived Stem Cell-Induced Vascularization Chondrogenesis Reconstruction of the external ear, whether due to congenital differences, trauma or cancer, has a significant impact on a patient’s quality of life. There are several corrective options available to patients, the most common being autologous reconstruction with costal cartilage. However, tissue-engineered constructs offer an alternative to traditional reconstruction methods. We are exploring chondrocyte sources to evaluate their chondrogenic potential with the hope of identifying a viable cell source for seeding cartilage scaffolds. This is done in collaboration with Miles Pfaff, MD, in our department. Publication: Identification of a Regenerative Protocol for Recellularizing Human Auricular Cartilage Scaffolds Micronanobubbles The development of ‘bubbled’ oxygenated solutions is used in wound healing, tissue transplantation storage solutions, acute major trauma injuries and in vitro laboratory settings to increase exposure to oxygenated solutions. A device was designed for oxygen generation in collaboration with UC Irvine Biomedical Engineering (BME). Publications: Micro/Nanobubble-Assisted Lipotransfer: In Vivo Evidence of Improved Graft Outcomes A Quantitative Assessment of Wound Healing With Oxygenated Micro/Nanobubbles in a Preclinical Burn Model Research Opportunities Undergraduates, Postgraduates & Researchers Our robust research program offers opportunities for undergraduates — through the UC Irvine BioSci 199 program — postgraduates and experienced researchers to collaborate on a variety of exciting and unique projects. Medical Students We also offer an annual fellowship for current medical students interested in gaining research experience. The program begins every year in August and is designed for third-year medical students who want to take a year off before returning for their fourth year. Collaborations & Center Contact Information We are open to collaboration. If you are affiliated with a research institution interested in collaborative opportunities or would like more information about the Department of Plastic Surgery’s CTE research projects, please contact: Alan Widgerow, MBBCh, FCS, MMed, FACS Research Chief & Director, Center for Tissue Engineering UC Irvine Department of Plastic Surgery 714-456-3482awidgero@hs.uci.edu Mary Ziegler, PhD Chief Scientist, Center for Tissue Engineering UC Irvine Department of Plastic Surgeryzieglerm@hs.uci.edu