دورية أكاديمية

Posterior talar process as a suitable cell source for treatment of cartilage and osteochondral defects of the talus.

التفاصيل البيبلوغرافية
العنوان: Posterior talar process as a suitable cell source for treatment of cartilage and osteochondral defects of the talus.
المؤلفون: Correia SI; 3Bs Research Group, Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4805-017, Barco, Guimarães, Portugal.; ICVS/3Bs, PT Government Associate Laboratory, Braga/Guimarães, Portugal., Silva-Correia J; 3Bs Research Group, Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4805-017, Barco, Guimarães, Portugal.; ICVS/3Bs, PT Government Associate Laboratory, Braga/Guimarães, Portugal., Pereira H; 3Bs Research Group, Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4805-017, Barco, Guimarães, Portugal.; ICVS/3Bs, PT Government Associate Laboratory, Braga/Guimarães, Portugal.; Clínica do Dragão - Espregueira-Mendes Sports Centre - FIFA Medical Centre of Excellence, F.C. Porto Stadium, Minho University and Porto University Research Centre, Portugal.; Orthopaedic Department Centro Hospitalar Póvoa de Varzim, Vila do Conde, Portugal., Canadas RF; 3Bs Research Group, Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4805-017, Barco, Guimarães, Portugal.; ICVS/3Bs, PT Government Associate Laboratory, Braga/Guimarães, Portugal., da Silva Morais A; 3Bs Research Group, Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4805-017, Barco, Guimarães, Portugal.; ICVS/3Bs, PT Government Associate Laboratory, Braga/Guimarães, Portugal., Frias AM; 3Bs Research Group, Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4805-017, Barco, Guimarães, Portugal.; Stemmatters, Biotecnologia e Medicina Regenerativa SA, 4805-017, Guimarães, Portugal., Sousa RA; 3Bs Research Group, Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4805-017, Barco, Guimarães, Portugal.; Stemmatters, Biotecnologia e Medicina Regenerativa SA, 4805-017, Guimarães, Portugal., van Dijk CN; Clínica do Dragão - Espregueira-Mendes Sports Centre - FIFA Medical Centre of Excellence, F.C. Porto Stadium, Minho University and Porto University Research Centre, Portugal.; Orthopaedic Department, Amsterdam Medical Centre, The Netherlands., Espregueira-Mendes J; 3Bs Research Group, Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4805-017, Barco, Guimarães, Portugal.; ICVS/3Bs, PT Government Associate Laboratory, Braga/Guimarães, Portugal.; Clínica do Dragão - Espregueira-Mendes Sports Centre - FIFA Medical Centre of Excellence, F.C. Porto Stadium, Minho University and Porto University Research Centre, Portugal., Reis RL; 3Bs Research Group, Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4805-017, Barco, Guimarães, Portugal.; ICVS/3Bs, PT Government Associate Laboratory, Braga/Guimarães, Portugal., Oliveira JM; 3Bs Research Group, Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4805-017, Barco, Guimarães, Portugal.; ICVS/3Bs, PT Government Associate Laboratory, Braga/Guimarães, Portugal.
المصدر: Journal of tissue engineering and regenerative medicine [J Tissue Eng Regen Med] 2017 Jul; Vol. 11 (7), pp. 1949-1962. Date of Electronic Publication: 2015 Oct 29.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: John Wiley & Sons Country of Publication: England NLM ID: 101308490 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1932-7005 (Electronic) Linking ISSN: 19326254 NLM ISO Abbreviation: J Tissue Eng Regen Med Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Chichester, West Sussex, UK : John Wiley & Sons
مواضيع طبية MeSH: Cartilage* , Cell Proliferation*, Talus/*cytology , Talus/*metabolism , Tissue Engineering/*methods, Humans
مستخلص: Osteochondral defects of the ankle are common lesions affecting the talar cartilage and subchondral bone. Current treatments include cell-based therapies but are frequently associated with donor-site morbidity. Our objective is to characterize the posterior process of the talus (SP) and the os trigonum (OT) tissues and investigate their potential as a new source of viable cells for application in tissue engineering and regenerative medicine. SP and OT tissues obtained from six patients were characterized by micro-computed tomography and histological, histomorphometric and immunohistochemical analyses. Proliferation and viability of isolated cells were evaluated by MTS assay, DNA quantification and live/dead staining. The TUNEL assay was performed to evaluate cell death by apoptosis. Moreover, the production of extracellular matrix was evaluated by toluidine blue staining, whereas cells phenotype was investigated by flow cytometry. Characterization of ankle explants showed the presence of a cartilage tissue layer in both SP and OT tissues, which represented at least 20%, on average, of the explant. The presence of type II collagen was detected in the extracellular matrix. Isolated cells presented a round morphology typical of chondrocytes. In in vitro studies, cells were viable and proliferating for up to 21 days of culture. No signs of apoptosis were detected. Flow-cytometry analysis revealed that isolated cells maintained the expression of several chondrocytic markers during culture. The results indicated that the SP and OT tissues were a reliable source of viable chondrocytes, which could find promising applications in ACI/MACI strategies with minimal concerns regarding donor zone complications. Copyright © 2015 John Wiley & Sons, Ltd.
(Copyright © 2015 John Wiley & Sons, Ltd.)
فهرسة مساهمة: Keywords: Stieda process; ankle; os trigonum; osteochondral lesions; regenerative medicine; talus lesions
تواريخ الأحداث: Date Created: 20151030 Date Completed: 20180326 Latest Revision: 20181101
رمز التحديث: 20231215
DOI: 10.1002/term.2092
PMID: 26510640
قاعدة البيانات: MEDLINE
الوصف
تدمد:1932-7005
DOI:10.1002/term.2092