Serveur d'exploration Chanson de Roland (version 6)

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Perfusion‐Decellularization of Porcine Lung and Trachea for Respiratory Bioengineering

Identifieur interne : 000117 ( Main/Exploration ); précédent : 000116; suivant : 000118

Perfusion‐Decellularization of Porcine Lung and Trachea for Respiratory Bioengineering

Auteurs : Alexander Weymann [Allemagne, Royaume-Uni] ; Nikhil Prakash Patil [Royaume-Uni] ; Anton Sabashnikov [Royaume-Uni] ; Sevil Korkmaz [Allemagne] ; Shiliang Li [Allemagne] ; Pal Soos [Hongrie] ; Roland Ishtok [Hongrie] ; Nicole Chaimow [Allemagne] ; Ines P Tzold [Allemagne] ; Natalie Czerny [Allemagne] ; Bastian Schmack [Allemagne] ; Aron-Frederik Popov [Royaume-Uni] ; Andre Rüdiger Simon [Royaume-Uni] ; Matthias Karck [Allemagne] ; Gabor Szabo [Allemagne]

Source :

RBID : ISTEX:07A6334A55338BD644164F7B381F9825932A1505

English descriptors

Abstract

Decellularization of native organs may provide an acellular tissue platform for organ regeneration. However, decellularization involves a trade‐off between removal of immunogenic cellular elements and preservation of biomechanical integrity. We sought to develop a bioartificial scaffold for respiratory tissue engineering by decellularization of porcine lungs and trachea while preserving organ architecture and vasculature. Lung–trachea preparations from 25 German Landrace pigs were perfused in a modified Langendorff circuit and decellularized by an SDC (sodium deoxycholate)‐based perfusion protocol. Decellularization was evaluated by histology and fluorescence microscopy, and residual DNA quantified spectrophotometrically and compared with controls. Airway compliance was evaluated by endotracheal intubation and mechanical ventilation to simulate physiological breathing‐induced stretch. Structural integrity was evaluated by bronchoscopy and biomechanical stress/strain analysis by measuring passive tensile strength, all compared with controls. Decellularized lungs and trachea lacked intracellular components but retained specific collagen fibers and elastin. Quantitative DNA analysis demonstrated a significant reduction of DNA compared with controls (32.8 ± 12.4 μg DNA/mg tissue vs. 179.7 ± 35.8 μg DNA/mg tissue, P < 0.05). Lungs and trachea decellularized by our perfusion protocol demonstrated increased airway compliance but preserved biomechanical integrity as compared with native tissue. Whole porcine lungs–tracheae can be successfully decellularized to create an acellular scaffold that preserves extracellular matrix and retains structral integrity and three‐dimensional architecture to provide a bioartifical platform for respiratory tissue engineering.

Url:
DOI: 10.1111/aor.12481


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<title level="j" type="main">Artificial Organs</title>
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<term>Acellular</term>
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<term>Airway compliance</term>
<term>Alexander weymann</term>
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<term>Artificial organ</term>
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<term>Cardiac surgery</term>
<term>Cell debris</term>
<term>Collagen formation</term>
<term>Component such</term>
<term>Decellularization</term>
<term>Decellularization protocol</term>
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<term>Maximal tensile strength</term>
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<term>Organ regeneration</term>
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<term>Protocol</term>
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<term>Remnant nuclear structure</term>
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<term>Room temperature</term>
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<term>Sloughed cell material</term>
<term>Static compliance</term>
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<term>Structral integrity</term>
<term>Substantial stiffening</term>
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<div type="abstract">Decellularization of native organs may provide an acellular tissue platform for organ regeneration. However, decellularization involves a trade‐off between removal of immunogenic cellular elements and preservation of biomechanical integrity. We sought to develop a bioartificial scaffold for respiratory tissue engineering by decellularization of porcine lungs and trachea while preserving organ architecture and vasculature. Lung–trachea preparations from 25 German Landrace pigs were perfused in a modified Langendorff circuit and decellularized by an SDC (sodium deoxycholate)‐based perfusion protocol. Decellularization was evaluated by histology and fluorescence microscopy, and residual DNA quantified spectrophotometrically and compared with controls. Airway compliance was evaluated by endotracheal intubation and mechanical ventilation to simulate physiological breathing‐induced stretch. Structural integrity was evaluated by bronchoscopy and biomechanical stress/strain analysis by measuring passive tensile strength, all compared with controls. Decellularized lungs and trachea lacked intracellular components but retained specific collagen fibers and elastin. Quantitative DNA analysis demonstrated a significant reduction of DNA compared with controls (32.8 ± 12.4 μg DNA/mg tissue vs. 179.7 ± 35.8 μg DNA/mg tissue, P < 0.05). Lungs and trachea decellularized by our perfusion protocol demonstrated increased airway compliance but preserved biomechanical integrity as compared with native tissue. Whole porcine lungs–tracheae can be successfully decellularized to create an acellular scaffold that preserves extracellular matrix and retains structral integrity and three‐dimensional architecture to provide a bioartifical platform for respiratory tissue engineering.</div>
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