Pulmonary Visceral Pleura Biomaterial: Elastin- and Collagen-Based Extracellular Matrix

Objective: The goal of the study is to determine the structural characteristics, mechanical properties, cytotoxicity, and biocompatibility of the pulmonary visceral pleura (PVP).Background: Collagen and elastin are the major components of the extracellular matrix. The PVP has an abundance of elastin...

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Main Authors: Xiao Lu, Ling Han, Ghassan S. Kassab
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-03-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fbioe.2022.796076/full
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author Xiao Lu
Ling Han
Ghassan S. Kassab
author_facet Xiao Lu
Ling Han
Ghassan S. Kassab
author_sort Xiao Lu
collection DOAJ
description Objective: The goal of the study is to determine the structural characteristics, mechanical properties, cytotoxicity, and biocompatibility of the pulmonary visceral pleura (PVP).Background: Collagen and elastin are the major components of the extracellular matrix. The PVP has an abundance of elastin and collagen that can serve as a potential biomaterial for clinical repair and reconstructions.Methods: The PVP was processed from swine and bovine lungs. Chemical analyses were used to determine collagen and elastin contents in the PVPs. Immunofluorescence microscopy was used to analyze the structure of the PVP. The stress–strain relationships and stress relaxation were determined by using the planar uniaxial test. The cytotoxicity of the PVP was tested in cultured cells. In in vivo evaluations, the PVP was implanted in the sciatic nerve and skin of rats.Results: Collagen and elastin contents are abundant in the PVP with larger proportions of elastin than in the bovine pericardium and porcine small intestinal submucosa. A microstructural analysis revealed that the elastin fibers were distributed throughout the PVP and the collagen was distributed mainly in the mesothelial basal lamina. The incremental moduli in stress–strain curves and relaxation moduli in the Maxwell–Wiechert model of PVP were approximately one-tenth of the bovine pericardium and small intestinal submucosa. The minimal cytotoxicity of the PVP was demonstrated. The axons proliferated in the PVP conduit guidance from proximal to distal sciatic nerves of rats. The neo-skin regenerated under the PVP skin substitute within 4 weeks.Conclusions: The PVP is composed of abundant collagen and elastin. The structural characteristics and mechanical compliance of the PVP render a suitable biological material for repair/reconstruction.
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spelling doaj.art-b6c64e89bd1044f89242bfc3c42ba69d2022-12-21T18:19:49ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852022-03-011010.3389/fbioe.2022.796076796076Pulmonary Visceral Pleura Biomaterial: Elastin- and Collagen-Based Extracellular MatrixXiao LuLing HanGhassan S. KassabObjective: The goal of the study is to determine the structural characteristics, mechanical properties, cytotoxicity, and biocompatibility of the pulmonary visceral pleura (PVP).Background: Collagen and elastin are the major components of the extracellular matrix. The PVP has an abundance of elastin and collagen that can serve as a potential biomaterial for clinical repair and reconstructions.Methods: The PVP was processed from swine and bovine lungs. Chemical analyses were used to determine collagen and elastin contents in the PVPs. Immunofluorescence microscopy was used to analyze the structure of the PVP. The stress–strain relationships and stress relaxation were determined by using the planar uniaxial test. The cytotoxicity of the PVP was tested in cultured cells. In in vivo evaluations, the PVP was implanted in the sciatic nerve and skin of rats.Results: Collagen and elastin contents are abundant in the PVP with larger proportions of elastin than in the bovine pericardium and porcine small intestinal submucosa. A microstructural analysis revealed that the elastin fibers were distributed throughout the PVP and the collagen was distributed mainly in the mesothelial basal lamina. The incremental moduli in stress–strain curves and relaxation moduli in the Maxwell–Wiechert model of PVP were approximately one-tenth of the bovine pericardium and small intestinal submucosa. The minimal cytotoxicity of the PVP was demonstrated. The axons proliferated in the PVP conduit guidance from proximal to distal sciatic nerves of rats. The neo-skin regenerated under the PVP skin substitute within 4 weeks.Conclusions: The PVP is composed of abundant collagen and elastin. The structural characteristics and mechanical compliance of the PVP render a suitable biological material for repair/reconstruction.https://www.frontiersin.org/articles/10.3389/fbioe.2022.796076/fulllungstructurecompliancebiomechanicsbiocompatibilitynerve
spellingShingle Xiao Lu
Ling Han
Ghassan S. Kassab
Pulmonary Visceral Pleura Biomaterial: Elastin- and Collagen-Based Extracellular Matrix
Frontiers in Bioengineering and Biotechnology
lung
structure
compliance
biomechanics
biocompatibility
nerve
title Pulmonary Visceral Pleura Biomaterial: Elastin- and Collagen-Based Extracellular Matrix
title_full Pulmonary Visceral Pleura Biomaterial: Elastin- and Collagen-Based Extracellular Matrix
title_fullStr Pulmonary Visceral Pleura Biomaterial: Elastin- and Collagen-Based Extracellular Matrix
title_full_unstemmed Pulmonary Visceral Pleura Biomaterial: Elastin- and Collagen-Based Extracellular Matrix
title_short Pulmonary Visceral Pleura Biomaterial: Elastin- and Collagen-Based Extracellular Matrix
title_sort pulmonary visceral pleura biomaterial elastin and collagen based extracellular matrix
topic lung
structure
compliance
biomechanics
biocompatibility
nerve
url https://www.frontiersin.org/articles/10.3389/fbioe.2022.796076/full
work_keys_str_mv AT xiaolu pulmonaryvisceralpleurabiomaterialelastinandcollagenbasedextracellularmatrix
AT linghan pulmonaryvisceralpleurabiomaterialelastinandcollagenbasedextracellularmatrix
AT ghassanskassab pulmonaryvisceralpleurabiomaterialelastinandcollagenbasedextracellularmatrix