DESCRIPTION (provided by applicant): Currently, there is no adequate treatment available for the replacement of tracheal segments larger than 6 cm. The goal of these studies is to develop and fabricate a functional trachea replacement in a rabbit model using tissue engineering principles, and to also fabricate a human-sized neotrachea using human cells in an athymic rat model. This laboratory has developed the methodology to produce large scaffold-free cartilage sheets, which when implanted in vivo and surrounded by fascia or muscle, produces a vascularized neotracheal construct. Rabbit ear and shoulder chondrocytes will be tested and optimized for cartilage sheet production and will be tested for their long-term stability and function in a trachea segmental defect model. The sheets are first fabricated in a custom double diffusion bioreactor and then implanted proximal to the future segmental repair site in the trachea where it is allowed to mature for approximately 12 weeks prior to segmental tracheal reconstruction. The neotrachea is transplanted along its vasculature into segmental tracheal defect and will be harvested at 4, 8 and 12 weeks postimplantation. Three distinct surgical formats will be tested including the direct transplant alone, transplant with a T-tube (to assist breathing and promote repair), and transplant with T-tube along with cheek mucosal free transplant. The harvested neotracheas are assessed by histologic and immunohistochemical methods including staining for glycosaminoglycans, and immunohistochemistry for collagens type I, II, and X, and elastin, examined, histologically, for structure, tissue integration, epithelialization, and are evaluated for biomechanical strength. Particular attention will be paid to the fibrosis, the formation of a mucous membrane, and also whether bone forms within the neotrachea. Alternative approaches to apply epithelial cells to the engineered tissue may be employed. The long-term goals are to develop the methodology to produce a functional trachea to repair segmental defects in rabbits, and to translate this technology to human derived cells. To this end, in parallel with the optimization study of rabbit chondrocytes, human chondrocytes will be obtained from the trachea, ear, nose and from articular surfaces and will be optimized for cartilage sheet formation by first testing a bank of growth factors and cytokines using a chondrogenesis aggregate culture assay system. Human chondrocyte-derived sheets will then be tested in an athymic rat model for their ability to form a human-sized neotrachea in vivo, and will be assessed by the histologic, biochemical and mechanical assays.
Public Health Relevance Statement
PUBLIC HEALTH RELEVANCE: Currently, there is no adequate treatment for large (6 cm or greater) trachea defects. The focus of this project is to use tissue engineering principles to fabricate a neo-trachea that can repair segmental defects in rabbits and to then apply these principles to fabricate a neo-trachea using human chondrocytes. The long-term goal this project seeks to develop a tissue engineering method to repair damaged tracheas in people.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AbdomenAttentionAutologousBiochemicalBiocompatibleBiological AssayBiomechanicsBioreactorsBone TissueBreathingCartilageCellsCheek structureChondrocytesChondrogenesisClinicalCollagen Type ICustomDefectDevelopmentDiffusionDimensionsEarElastinEndoscopesEngineeringEpithelial CellsFasciaFibrosisFutureGlycosaminoglycansGoalsGrowth FactorHarvestHealthHistologicHistologyHumanImmunohistochemistryImplantIn VitroLaboratoriesLongitudinal StudiesMechanicsMethodologyMethodsModelingMucous MembraneMuscleNoseNude RatsOperative Surgical ProceduresOryctolagus cuniculusPalpationPhasePostoperative PeriodProductionPropertyShoulderSiliconesSiteSourceStagingStaining methodStainsStructureStructure of respiratory epitheliumSurfaceSurgical FlapsSystemTechnologyTestingThickTissue EngineeringTissuesTracheaTranslatingTranslationsTransplantationTubearticular cartilagebaseboneclinical applicationclinically relevantcytokinedesignin vivoin vivo Modelpre-clinicalreconstructionrepairedresearch studyscaffoldsoundtool
National Institute of Dental and Craniofacial Research
CFDA Code
121
DUNS Number
051113330
UEI
FXKMA43NTV21
Project Start Date
01-December-2014
Project End Date
30-November-2015
Budget Start Date
01-December-2014
Budget End Date
30-November-2015
Project Funding Information for 2014
Total Funding
$395,724
Direct Costs
$251,254
Indirect Costs
$144,470
Year
Funding IC
FY Total Cost by IC
2014
National Institute of Dental and Craniofacial Research
$395,724
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 7R01DE015322-11
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 7R01DE015322-11
Patents
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 7R01DE015322-11
Clinical Studies
No Clinical Studies information available for 7R01DE015322-11
News and More
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History
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