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dc.contributor.authorBOZKURT, Erol
dc.contributor.authorCansiz, Harun
dc.contributor.authorYigit, Ozgur
dc.contributor.authorBatioglu-Karaaltin, Ayşegül
dc.contributor.authorKaraaltin, Mehmet Veli
dc.contributor.authorOVALI, Ercument
dc.contributor.authorKONGUR, Merve
dc.contributor.authorInan, Oznur
dc.date.accessioned2021-03-05T10:45:39Z
dc.date.available2021-03-05T10:45:39Z
dc.date.issued2015
dc.identifier.citationBatioglu-Karaaltin A., Karaaltin M. V. , OVALI E., Yigit O., KONGUR M., Inan O., BOZKURT E., Cansiz H., "In Vivo Tissue-Engineered Allogenic Trachea Transplantation in Rabbits: A Preliminary Report", STEM CELL REVIEWS AND REPORTS, cilt.11, ss.347-356, 2015
dc.identifier.issn2629-3269
dc.identifier.othervv_1032021
dc.identifier.otherav_a4caf645-35db-46a4-abcb-d35a4b3af86d
dc.identifier.urihttp://hdl.handle.net/20.500.12627/110217
dc.identifier.urihttps://doi.org/10.1007/s12015-014-9570-8
dc.description.abstractConventional tracheal reconstruction techniques are not successful at restoring functional units in situations with extensive damage involving more than half the length of the trachea. For the first time, we investigated in vivo tissue-engineered trachea regeneration from a decellularized cadaveric trachea matrix with seeded adult adipose tissue-derived mesenchymal stem cells (MSCs) and investigated the integration of the matrix into the recipient tracheal side. For the procedure, 1.8-cm grafts were prepared from 3.5-cm tracheas of three donor rabbits. Then, tracheal grafts were rendered nonimmunogenic using a decellularization technique. MSCs isolated from recipient rabbit adipose tissue were cultured and marked before being seeded in the decellularized matrix. A total of 1.8 cm of the recipient tracheas was replaced with either a decellularized tracheal matrix (group 1) or tracheal matrix-seeded MSCs (group 2). Rabbits survived 17 +/- 2 days in the first group, and the causes of death were separation in the anastomosis region, airway obstruction, and infection. In the second group, animals were sacrificed on the 30th, 60th, and 90th days of follow-up. Histopathological analysis revealed the integration of MSCs seeded-decellularized cadaveric tracheas to the recipient tracheal sides and increased angiogenesis. The MSCs were traced by fluorescence microscopy in the ciliated epithelium, under the epithelium, and in the cartilage of the integrated new trachea. Tracheas generated by autologous cells and tissue-engineering techniques will be a great source for the treatment of life-threatening tracheal injuries after the completion of related studies.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectHÜCRE VE DOKU MÜHENDİSLİĞİ
dc.subjectBiyoloji ve Biyokimya
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectHÜCRE BİYOLOJİSİ
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTIP, ARAŞTIRMA VE DENEYSEL
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectHistoloji-Embriyoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Ekoloji ve Hidroklimatoloji
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.titleIn Vivo Tissue-Engineered Allogenic Trachea Transplantation in Rabbits: A Preliminary Report
dc.typeMakale
dc.relation.journalSTEM CELL REVIEWS AND REPORTS
dc.contributor.departmentAcıbadem Mehmet Ali Aydınlar Üniversitesi , ,
dc.identifier.volume11
dc.identifier.issue2
dc.identifier.startpage347
dc.identifier.endpage356
dc.contributor.firstauthorID102384


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