Source:http://linkedlifedata.com/resource/pubmed/id/12760965
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
2003-5-22
|
pubmed:abstractText |
Extensive tracheal defects may pose a life-threatening dilemma. Although tracheal transplantation may represent a reconstructive solution, very little is known regarding the immunobiology and behavior of tracheal allografts. The objective of this study was to assess the pattern and kinetics of re-epithelialization of orthotopic tracheal allografts in immunosuppressed recipients. Thirty-eight age-matched mice were randomly assigned to five experimental groups. BALB/c donor tracheal segments were orthotopically transplanted into either syngeneic BALB/c or MHC mismatched allogeneic C57BL/6 recipients with and without immunosuppression. On post-transplant days 7, 14, 28, 48, and 62, animals from each group were evaluated by serial histology, electron microscopy, and serial immunohistochemical analysis for mucosal phenotype, re-epithelialization pattern, and lymphocyte subpopulations. Nonimmunosuppressed recipients underwent recipient-derived basal cell re-epithelialization by Day 48, with differentiation into a sparse population of ciliated columnar epithelium by Day 62, whereas immunosuppressed recipients underwent basal cell re-epithelialization 28 d after transplantation and differentiation into a dense population of ciliated columnar epithelium by Day 48. The re-epithelialization process occurred in a definable pattern that was significantly enhanced with the addition of immunosuppression. Orthotopic tracheal transplants undergo progressive re-epithelialization with recipient-derived basal cells that differentiate into ciliated columnar epithelium in a definable pattern that is enhanced with the addition of immunosuppression.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
1044-1549
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
28
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
673-81
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:12760965-Animals,
pubmed-meshheading:12760965-Cell Division,
pubmed-meshheading:12760965-Epithelial Cells,
pubmed-meshheading:12760965-Graft Survival,
pubmed-meshheading:12760965-Immunosuppression,
pubmed-meshheading:12760965-Kinetics,
pubmed-meshheading:12760965-Mice,
pubmed-meshheading:12760965-Mice, Inbred BALB C,
pubmed-meshheading:12760965-Mice, Inbred C57BL,
pubmed-meshheading:12760965-Microscopy, Electron,
pubmed-meshheading:12760965-Regeneration,
pubmed-meshheading:12760965-Respiratory Mucosa,
pubmed-meshheading:12760965-Trachea,
pubmed-meshheading:12760965-Transplantation, Homologous,
pubmed-meshheading:12760965-Transplantation, Isogeneic
|
pubmed:year |
2003
|
pubmed:articleTitle |
The kinetics and pattern of tracheal allograft re-epithelialization.
|
pubmed:affiliation |
Department of Otolaryngology-Head and Neck Surgery, Mount Sinai School of Medicine, One Gustave Levy Place, New York, NY 10029, USA. eric.genden@mssm.edu
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|