Show simple item record

dc.contributor.authorRamazanoğlu, Mustafa
dc.contributor.authorKoyuncu, A. C. Calikoglu
dc.contributor.authorPekozer, G. Gurel
dc.contributor.authorKose, G. Torun
dc.contributor.authorHASIRCI, VASIF NEJAT
dc.date.accessioned2021-03-04T10:36:19Z
dc.date.available2021-03-04T10:36:19Z
dc.date.issued2017
dc.identifier.citationKoyuncu A. C. C. , Pekozer G. G. , Ramazanoğlu M., Kose G. T. , HASIRCI V. N. , "Cartilage tissue engineering on macroporous scaffolds using human tooth germ stem cells", JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, cilt.11, sa.3, ss.765-777, 2017
dc.identifier.issn1932-6254
dc.identifier.othervv_1032021
dc.identifier.otherav_6e080957-d073-4501-b747-b3df8948ab84
dc.identifier.urihttp://hdl.handle.net/20.500.12627/75983
dc.identifier.urihttps://doi.org/10.1002/term.1975
dc.description.abstractThe main objective was to study cartilage regeneration through differentiation of human tooth germ stem cells (HTGSCs) into chondrocytes on different three-dimensional (3D) scaffolds (PCL, PLLA and PCL-PLLA). Scaffold topographies were studied by scanning electron microscopy and it was found that the scaffolds had interconnected macroporous structures. HTGSCs were isolated from impacted third molar tooth germs of young adult patients and grown for 3 weeks on the scaffolds in chondrogenic differentiation medium. Cell proliferation on the scaffolds was determined by MTS assay and it was observed that all scaffolds supported cell proliferation. Immunostaining was carried out for morphological and differentiation analyses. Immunohistochemical analyses revealed that the cells attached onto the scaffolds and deposited cartilage-specific extracellular matrix (ECM). Real-time PCR was performed to determine the expression levels of cartilage-specific genes. After 21 days of incubation in cartilage differentiation medium, expression of collagen type II increased only in the cells seeded onto PCL-PLLA blend scaffolds. Similarly, aggrecan expression was the highest on PCL-PLLA scaffolds after 3weeks. These results suggest that all the scaffolds, and especially PCL-PLLA, were suitable for chondrogenic differentiation of HTGSCs. Copyright (C) 2015 John Wiley & Sons, Ltd.
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectMühendislik ve Teknoloji
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyoloji ve Biyokimya
dc.subjectHÜCRE VE DOKU MÜHENDİSLİĞİ
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectBİYOTEKNOLOJİ VE UYGULAMALI MİKROBİYOLOJİ
dc.subjectMikrobiyoloji
dc.subjectHÜCRE BİYOLOJİSİ
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectMÜHENDİSLİK, BİYOMEDİKSEL
dc.subjectMühendislik
dc.subjectMühendislik, Bilişim ve Teknoloji (ENG)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectBiyokimya
dc.subjectHistoloji-Embriyoloji
dc.subjectBiyomedikal Mühendisliği
dc.subjectYaşam Bilimleri
dc.subjectBiyoteknoloji
dc.titleCartilage tissue engineering on macroporous scaffolds using human tooth germ stem cells
dc.typeMakale
dc.relation.journalJOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE
dc.contributor.departmentYeditepe Üniversitesi , ,
dc.identifier.volume11
dc.identifier.issue3
dc.identifier.startpage765
dc.identifier.endpage777
dc.contributor.firstauthorID77787


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record