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In vitro fabrication of autologous living tissue-engineered vascular grafts based on prenatally harvested ovine amniotic fluid-derived stem cells.
Weber, Benedikt; Kehl, Debora; Bleul, Ulrich; Behr, Luc; Sammut, Sébastien; Frese, Laura; Ksiazek, Agnieszka; Achermann, Josef; Stranzinger, Gerald; Robert, Jérôme; Sanders, Bart; Sidler, Michele; Brokopp, Chad E; Proulx, Steven T; Frauenfelder, Thomas; Schoenauer, Roman; Emmert, Maximilian Y; Falk, Volkmar; Hoerstrup, Simon P.
Afiliação
  • Weber B; Swiss Centre for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
  • Kehl D; Clinic for Cardiovascular Surgery and Department of Surgical Research, University Hospital of Zurich, Zurich, Switzerland.
  • Bleul U; Swiss Centre for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
  • Behr L; Clinic for Cardiovascular Surgery and Department of Surgical Research, University Hospital of Zurich, Zurich, Switzerland.
  • Sammut S; Clinic of Reproductive Medicine, Department of Food Animals, Vetsuisse-Faculty University of Zurich, Zurich, Switzerland.
  • Frese L; IMM Recherche, Institute Mutualiste Montsouris, Paris, France.
  • Ksiazek A; IMM Recherche, Institute Mutualiste Montsouris, Paris, France.
  • Achermann J; Swiss Centre for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
  • Stranzinger G; Clinic for Cardiovascular Surgery and Department of Surgical Research, University Hospital of Zurich, Zurich, Switzerland.
  • Robert J; Swiss Centre for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
  • Sanders B; Clinic for Cardiovascular Surgery and Department of Surgical Research, University Hospital of Zurich, Zurich, Switzerland.
  • Sidler M; Human Genetics Laboratory, Genetica AG, Zurich, Switzerland.
  • Brokopp CE; Breeding Biology Group, Swiss Federal Institute of Technology, Zurich, Switzerland.
  • Proulx ST; Swiss Centre for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
  • Frauenfelder T; Clinic for Cardiovascular Surgery and Department of Surgical Research, University Hospital of Zurich, Zurich, Switzerland.
  • Schoenauer R; Institute of Clinical Chemistry, University Hospital Zurich, Zurich, Switzerland.
  • Emmert MY; Department of Biomedical Engineering, Soft Tissue Biomechanics and Tissue Engineering, Eindhoven University of Technology, the Netherlands.
  • Falk V; Musculo-sceletal Research Unit, Vetsuisse-Faculty, University of Zurich, Zurich, Switzerland.
  • Hoerstrup SP; Swiss Centre for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
J Tissue Eng Regen Med ; 10(1): 52-70, 2016 Jan.
Article em En | MEDLINE | ID: mdl-23881794
ABSTRACT
Amniotic fluid cells (AFCs) have been proposed as a valuable source for tissue engineering and regenerative medicine. However, before clinical implementation, rigorous evaluation of this cell source in clinically relevant animal models accepted by regulatory authorities is indispensable. Today, the ovine model represents one of the most accepted preclinical animal models, in particular for cardiovascular applications. Here, we investigate the isolation and use of autologous ovine AFCs as cell source for cardiovascular tissue engineering applications. Fetal fluids were aspirated in vivo from pregnant ewes (n = 9) and from explanted uteri post mortem at different gestational ages (n = 91). Amniotic non-allantoic fluid nature was evaluated biochemically and in vivo samples were compared with post mortem reference samples. Isolated cells revealed an immunohistochemical phenotype similar to ovine bone marrow-derived mesenchymal stem cells (MSCs) and showed expression of stem cell factors described for embryonic stem cells, such as NANOG and STAT-3. Isolated ovine amniotic fluid-derived MSCs were screened for numeric chromosomal aberrations and successfully differentiated into several mesodermal phenotypes. Myofibroblastic ovine AFC lineages were then successfully used for the in vitro fabrication of small- and large-diameter tissue-engineered vascular grafts (n = 10) and cardiovascular patches (n = 34), laying the foundation for the use of this relevant pre-clinical in vivo assessment model for future amniotic fluid cell-based therapeutic applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prótese Vascular / Engenharia Tecidual / Âmnio / Líquido Amniótico Tipo de estudo: Prognostic_studies Limite: Animals / Pregnancy Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prótese Vascular / Engenharia Tecidual / Âmnio / Líquido Amniótico Tipo de estudo: Prognostic_studies Limite: Animals / Pregnancy Idioma: En Ano de publicação: 2016 Tipo de documento: Article