Long-term cryopreservation of decellularised oesophagi for tissue engineering clinical application.

Oesophageal tissue engineering is a therapeutic alternative when oesophageal replacement is required. Decellularised scaffolds are ideal as they are derived from tissue-specific extracellular matrix and are non-immunogenic. However, appropriate preservation may significantly affect scaffold behaviou...

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Main Authors: Luca Urbani, Panagiotis Maghsoudlou, Anna Milan, Maria Menikou, Charlotte Klara Hagen, Giorgia Totonelli, Carlotta Camilli, Simon Eaton, Alan Burns, Alessandro Olivo, Paolo De Coppi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0179341&type=printable
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author Luca Urbani
Panagiotis Maghsoudlou
Anna Milan
Maria Menikou
Charlotte Klara Hagen
Giorgia Totonelli
Carlotta Camilli
Simon Eaton
Alan Burns
Alessandro Olivo
Paolo De Coppi
author_facet Luca Urbani
Panagiotis Maghsoudlou
Anna Milan
Maria Menikou
Charlotte Klara Hagen
Giorgia Totonelli
Carlotta Camilli
Simon Eaton
Alan Burns
Alessandro Olivo
Paolo De Coppi
author_sort Luca Urbani
collection DOAJ
description Oesophageal tissue engineering is a therapeutic alternative when oesophageal replacement is required. Decellularised scaffolds are ideal as they are derived from tissue-specific extracellular matrix and are non-immunogenic. However, appropriate preservation may significantly affect scaffold behaviour. Here we aim to prove that an effective method for short- and long-term preservation can be applied to tissue engineered products allowing their translation to clinical application. Rabbit oesophagi were decellularised using the detergent-enzymatic treatment (DET), a combination of deionised water, sodium deoxycholate and DNase-I. Samples were stored in phosphate-buffered saline solution at 4°C (4°C) or slow cooled in medium with 10% Me2SO at -1°C/min followed by storage in liquid nitrogen (SCM). Structural and functional analyses were performed prior to and after 2 and 4 weeks and 3 and 6 months of storage under each condition. Efficient decellularisation was achieved after 2 cycles of DET as determined with histology and DNA quantification, with preservation of the ECM. Only the SCM method, commonly used for cell storage, maintained the architecture and biomechanical properties of the scaffold up to 6 months. On the contrary, 4°C method was effective for short-term storage but led to a progressive distortion and degradation of the tissue architecture at the following time points. Efficient storage allows a timely use of decellularised oesophagi, essential for clinical translation. Here we describe that slow cooling with cryoprotectant solution in liquid nitrogen vapour leads to reliable long-term storage of decellularised oesophageal scaffolds for tissue engineering purposes.
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spelling doaj-art-70a06bef3ce946ff8f202a5cbfe8b3362025-08-20T02:31:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01126e017934110.1371/journal.pone.0179341Long-term cryopreservation of decellularised oesophagi for tissue engineering clinical application.Luca UrbaniPanagiotis MaghsoudlouAnna MilanMaria MenikouCharlotte Klara HagenGiorgia TotonelliCarlotta CamilliSimon EatonAlan BurnsAlessandro OlivoPaolo De CoppiOesophageal tissue engineering is a therapeutic alternative when oesophageal replacement is required. Decellularised scaffolds are ideal as they are derived from tissue-specific extracellular matrix and are non-immunogenic. However, appropriate preservation may significantly affect scaffold behaviour. Here we aim to prove that an effective method for short- and long-term preservation can be applied to tissue engineered products allowing their translation to clinical application. Rabbit oesophagi were decellularised using the detergent-enzymatic treatment (DET), a combination of deionised water, sodium deoxycholate and DNase-I. Samples were stored in phosphate-buffered saline solution at 4°C (4°C) or slow cooled in medium with 10% Me2SO at -1°C/min followed by storage in liquid nitrogen (SCM). Structural and functional analyses were performed prior to and after 2 and 4 weeks and 3 and 6 months of storage under each condition. Efficient decellularisation was achieved after 2 cycles of DET as determined with histology and DNA quantification, with preservation of the ECM. Only the SCM method, commonly used for cell storage, maintained the architecture and biomechanical properties of the scaffold up to 6 months. On the contrary, 4°C method was effective for short-term storage but led to a progressive distortion and degradation of the tissue architecture at the following time points. Efficient storage allows a timely use of decellularised oesophagi, essential for clinical translation. Here we describe that slow cooling with cryoprotectant solution in liquid nitrogen vapour leads to reliable long-term storage of decellularised oesophageal scaffolds for tissue engineering purposes.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0179341&type=printable
spellingShingle Luca Urbani
Panagiotis Maghsoudlou
Anna Milan
Maria Menikou
Charlotte Klara Hagen
Giorgia Totonelli
Carlotta Camilli
Simon Eaton
Alan Burns
Alessandro Olivo
Paolo De Coppi
Long-term cryopreservation of decellularised oesophagi for tissue engineering clinical application.
PLoS ONE
title Long-term cryopreservation of decellularised oesophagi for tissue engineering clinical application.
title_full Long-term cryopreservation of decellularised oesophagi for tissue engineering clinical application.
title_fullStr Long-term cryopreservation of decellularised oesophagi for tissue engineering clinical application.
title_full_unstemmed Long-term cryopreservation of decellularised oesophagi for tissue engineering clinical application.
title_short Long-term cryopreservation of decellularised oesophagi for tissue engineering clinical application.
title_sort long term cryopreservation of decellularised oesophagi for tissue engineering clinical application
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0179341&type=printable
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