Loss of esophageal tissue from congenital and acquired abnormalities is often surgically managed with autologous gastrointestinal interposition grafts in order to restore organ continuity. Unfortunately, these approaches are associated with severe adverse complications such as esophageal dysmotility, dysphagia, and donor site morbidity. Silk fibroin (SF) biomaterials provide an exceptional combination of physical characteristics including high tensile strength and elasticity, diverse processing flexibility, and tunable degradability that are well suited to support esophageal function. Therefore, these scaffolds may overcome the deleterious side-effects associated with conventional reconstructive techniques and serve as ?off-the-shelf? grafts for esophageal tissue repair. By understanding the role of the innate immune response in facilitating constructive remodeling of esophageal defects, we will design SF implants with selective microenvironmental cues sufficient to modulate macrophage activation phenotypes toward maximal regenerative outcomes. In this proposal, we will test the overall hypothesis that: acellular SF matrices promote functional restoration of esophageal defects via CD206+ M2a macrophage-dependent constructive remodeling.
The specific aims of the application are:
Specific Aim 1 : Develop SF grafts for functional repair of long-gap esophageal defects in a preclinical animal model.
Specific Aim 2 : Determine the impact of CD206+ M2a macrophages on scaffold mediated, constructive remodeling of esophageal defects.
Specific Aim 3 : Determine the efficacy of immunomodulatory SF grafts to maximize constructive remodeling and restore organ function in esophageal stricture disease.

Public Health Relevance

The results of this proposal are anticipated to produce new tissue repair modalities that will overcome current limitations in esophagoplasty and enhance our knowledge of the impact of the innate host immune response in dictating constructive remodeling within the esophagus. We seek to expand our knowledge of the nature, extent, and significance of biomaterial configurations necessary to optimize functional tissue replacement of the esophagus. We anticipate the results of this study will provide new information that is wider in scope than our specific goals and which may be applicable for repair of other gastrointestinal tissues and visceral hollow organs in general.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
7R01DK107568-05
Application #
10039432
Study Section
Bioengineering, Technology and Surgical Sciences Study Section (BTSS)
Program Officer
Greenwel, Patricia
Project Start
2019-10-12
Project End
2021-06-30
Budget Start
2019-10-12
Budget End
2020-06-30
Support Year
5
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of California Irvine
Department
Urology
Type
Schools of Medicine
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92617
Algarrahi, Khalid; Franck, Debra; Savarino, Alyssa et al. (2018) Bilayer silk fibroin grafts support functional oesophageal repair in a rodent model of caustic injury. J Tissue Eng Regen Med 12:e1068-e1075
Algarrahi, Khalid; Franck, Debra; Cristofaro, Vivian et al. (2018) Bi-layer silk fibroin grafts support functional tissue regeneration in a porcine model of onlay esophagoplasty. J Tissue Eng Regen Med 12:e894-e904