GMP compliant isolation of mucosal epithelial cells and fibroblasts from biopsy samples for clinical tissue engineering

Abstract Engineered epithelial cell sheets for clinical replacement of non-functional upper aerodigestive tract mucosa are regulated as medicinal products and should be manufactured to the standards of good manufacturing practice (GMP). The current gold standard for growth of epithelial cells for re...

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Main Authors: Angela Tait, Toby Proctor, Nick J. I. Hamilton, Martin A. Birchall, Mark W. Lowdell
Format: Article
Language:English
Published: Nature Publishing Group 2021-06-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-91939-0
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spelling doaj-8f2673ced80b44e8beb594861f87e6b82021-06-13T11:37:51ZengNature Publishing GroupScientific Reports2045-23222021-06-0111111210.1038/s41598-021-91939-0GMP compliant isolation of mucosal epithelial cells and fibroblasts from biopsy samples for clinical tissue engineeringAngela Tait0Toby Proctor1Nick J. I. Hamilton2Martin A. Birchall3Mark W. Lowdell4Cancer Institute, Department of Haematology, University College LondonDepartment of Biochemical Engineering, University College LondonInstitute of Ophthalmology, University College LondonUCL Ear Institute, University College LondonCancer Institute, Department of Haematology, University College LondonAbstract Engineered epithelial cell sheets for clinical replacement of non-functional upper aerodigestive tract mucosa are regulated as medicinal products and should be manufactured to the standards of good manufacturing practice (GMP). The current gold standard for growth of epithelial cells for research utilises growth arrested murine 3T3 J2 feeder layers, which are not available for use as a GMP compliant raw material. Using porcine mucosal tissue, we demonstrate a new method for obtaining and growing non-keratinised squamous epithelial cells and fibroblast cells from a single biopsy, replacing the 3T3 J2 with a growth arrested primary fibroblast feeder layer and using pooled Human Platelet lysate (HPL) as the media serum supplement to replace foetal bovine serum (FBS). The initial isolation of the cells was semi-automated using an Octodissociator and the resultant cell suspension cryopreservation for future use. When compared to the gold standard of 3T3 J2 and FBS containing medium there was no reduction in growth, viability, stem cell population or ability to differentiate to mature epithelial cells. Furthermore, this method was replicated with Human buccal tissue, providing cells of sufficient quality and number to create a tissue engineered sheet.https://doi.org/10.1038/s41598-021-91939-0
collection DOAJ
language English
format Article
sources DOAJ
author Angela Tait
Toby Proctor
Nick J. I. Hamilton
Martin A. Birchall
Mark W. Lowdell
spellingShingle Angela Tait
Toby Proctor
Nick J. I. Hamilton
Martin A. Birchall
Mark W. Lowdell
GMP compliant isolation of mucosal epithelial cells and fibroblasts from biopsy samples for clinical tissue engineering
Scientific Reports
author_facet Angela Tait
Toby Proctor
Nick J. I. Hamilton
Martin A. Birchall
Mark W. Lowdell
author_sort Angela Tait
title GMP compliant isolation of mucosal epithelial cells and fibroblasts from biopsy samples for clinical tissue engineering
title_short GMP compliant isolation of mucosal epithelial cells and fibroblasts from biopsy samples for clinical tissue engineering
title_full GMP compliant isolation of mucosal epithelial cells and fibroblasts from biopsy samples for clinical tissue engineering
title_fullStr GMP compliant isolation of mucosal epithelial cells and fibroblasts from biopsy samples for clinical tissue engineering
title_full_unstemmed GMP compliant isolation of mucosal epithelial cells and fibroblasts from biopsy samples for clinical tissue engineering
title_sort gmp compliant isolation of mucosal epithelial cells and fibroblasts from biopsy samples for clinical tissue engineering
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-06-01
description Abstract Engineered epithelial cell sheets for clinical replacement of non-functional upper aerodigestive tract mucosa are regulated as medicinal products and should be manufactured to the standards of good manufacturing practice (GMP). The current gold standard for growth of epithelial cells for research utilises growth arrested murine 3T3 J2 feeder layers, which are not available for use as a GMP compliant raw material. Using porcine mucosal tissue, we demonstrate a new method for obtaining and growing non-keratinised squamous epithelial cells and fibroblast cells from a single biopsy, replacing the 3T3 J2 with a growth arrested primary fibroblast feeder layer and using pooled Human Platelet lysate (HPL) as the media serum supplement to replace foetal bovine serum (FBS). The initial isolation of the cells was semi-automated using an Octodissociator and the resultant cell suspension cryopreservation for future use. When compared to the gold standard of 3T3 J2 and FBS containing medium there was no reduction in growth, viability, stem cell population or ability to differentiate to mature epithelial cells. Furthermore, this method was replicated with Human buccal tissue, providing cells of sufficient quality and number to create a tissue engineered sheet.
url https://doi.org/10.1038/s41598-021-91939-0
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