Tissue Engineering for Regeneration of the Tracheal Epithelium
Tissue Engineering for Regeneration of the Tracheal Epithelium
复制标题
DOI:
10.1177/000348940611500704
复制
发表时间:
2006-07
期刊:
影响因子:
--
通讯作者:
Yukio Nomoto;Teruhisa Suzuki;Y. Tada;Ken Kobayashi;M. Miyake;A. Hazama;I. Wada;S. Kanemaru;Tatsuo Nakamura;K. Omori
中科院分区:
文献类型:
--
作者:
Yukio Nomoto;Teruhisa Suzuki;Y. Tada;Ken Kobayashi;M. Miyake;A. Hazama;I. Wada;S. Kanemaru;Tatsuo Nakamura;K. Omori
Objectives: The slowness of epithelialization on the artificial trachea that has been successfully used in humans is a problem. The purpose of this study was to develop a way to regenerate the epithelium on the surface of this artificial trachea. Methods: In an in vitro study, isolated rat tracheal epithelial cells were seeded on a collagenous gel that was stratified on a collagenous sponge. Histologic and immunohistochemical examinations were made. In an in vivo study, we transplanted grafts with green fluorescent protein–positive tracheal epithelial cells onto the tracheal defects of normal rats. At 3, 7, 14, and 30 days after the operation, histologic and immunohistochemical examinations were made. Results: In the in vitro study, the 3 layers — the epithelium, gel, and sponge — could be observed. The epithelium expressed cytokeratin 14, cytokeratin 18, and occludin. In the in vivo study, the artificial trachea was covered with epithelium at 3 days after operation, and then the epithelium differentiated from single- or double-stratified squamous epithelium into columnar ciliated epithelium. Green fluorescent protein–positive cells were found 3 days after operation. Conclusions: We believe that the method used in our experiment is an effective way to regenerate the epithelium on the surface of an artificial trachea. With further experimentation, this method should be suitable for clinical application.