Systemic inflammation and multiple organ failure associated with trauma are a major cause of mortality and morbidity in American soldiers and veterans. Gut barrier dysfunction plays a critical role in the development of posttraumatic complications such as sepsis by providing the major site for plasma leakage and bacterial translocation to the circulation. Despite the well- recognized importance of gut dysfunction in the pathogenesis of posttraumatic complications, the intestinal permeability response to severe burns, a major form of trauma, has not been well characterized, and its cellular and molecular mechanisms remain poorly understood. The goal of this study is to elucidate the cell-specific mechanisms of leaky guts during thermal injury. We propose to define the function, regulation and molecular mechanisms of palmitoylation in mediating gut epithelial hyperpermeability during thermal injury. The hypothesis to be tested is that burn injury stimulates protein palmitoylation in the gut epithelial cells through upregulation of DHHC isoforms. Palmitoylation contributes to the pathogenesis of burn-induced gut hyperpermeability by stimulating ROCK-dependent cytoskeleton contraction and claudins/ZO2- mediated junction dissociation in the epithelial cells leading to epithelial barrier failure.
Three specific aims are developed in this proposal to: 1) study the function and regulation of palmitoylation in gut epithelial barrier injury, 2). examine the regulatory role of palmitoylation n gut epithelium during thermal injury, and 3) identify molecular targets of palmitoylation in mediating epithelial hyperpermeability. The study design employs complimentary in vivo, ex vivo, and in vitro models that incorporate molecular and genetic approaches into physiological experiments under clinically relevant trauma conditions. The significance of this study lies in the potential to identify a new role of protein palmitoylation in pathogenesis during trauma. Data derived from the research work will not only contribute to the advancement of gastrointestinal pathobiology, but also has clinical implications in the development of effective therapies or surgical interventions against gut barrier injury in patients with trauma or inflammatory diseases.

Public Health Relevance

Trauma is a major cause of mortality and morbidity in American soldiers and veterans. As a typical form of trauma, thermal injury results from flame/chemical burns in combat or related fire or scald accidents. Despite the improved critical care and wound management, posttraumatic complications remain a life-threatening problem that causes extended hospital stay. The gut plays an important role in developing multiple organ complications following a severe burn. In particular, gut barrier failure contributes to systemic inflammatory syndrome and sepsis. This study provides a comprehensive evaluation of the role of protein palmitoylation in mediation of intestinal hyperpermeability during burn-induced inflammation. The research work has potential impact on the development of surgical or medical interventions against gut barrier injury in VA patients with trauma or inflammatory diseases.

Agency
National Institute of Health (NIH)
Type
Non-HHS Research Projects (I01)
Project #
2I01BX000799-05
Application #
8734716
Study Section
Surgery (SURG)
Project Start
Project End
Budget Start
Budget End
Support Year
5
Fiscal Year
2014
Total Cost
Indirect Cost
Name
James A. Haley VA Medical Center
Department
Type
DUNS #
City
Tampa
State
FL
Country
United States
Zip Code
33612