Cargando…

Long-term expansion of primary equine keratinocytes that maintain the ability to differentiate into stratified epidermis

BACKGROUND: Skin injuries in horses frequently lead to chronic wounds that lack a keratinocyte cover essential for healing. The limited proliferation of equine keratinocytes using current protocols has limited their use for regenerative medicine. Previously, equine induced pluripotent stem cells (ei...

Descripción completa

Detalles Bibliográficos
Autores principales: Alkhilaiwi, Faris, Wang, Liqing, Zhou, Dan, Raudsepp, Terje, Ghosh, Sharmila, Paul, Siddartha, Palechor-Ceron, Nancy, Brandt, Sabine, Luff, Jennifer, Liu, Xuefeng, Schlegel, Richard, Yuan, Hang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032561/
https://www.ncbi.nlm.nih.gov/pubmed/29973296
http://dx.doi.org/10.1186/s13287-018-0918-x
_version_ 1783337525294661632
author Alkhilaiwi, Faris
Wang, Liqing
Zhou, Dan
Raudsepp, Terje
Ghosh, Sharmila
Paul, Siddartha
Palechor-Ceron, Nancy
Brandt, Sabine
Luff, Jennifer
Liu, Xuefeng
Schlegel, Richard
Yuan, Hang
author_facet Alkhilaiwi, Faris
Wang, Liqing
Zhou, Dan
Raudsepp, Terje
Ghosh, Sharmila
Paul, Siddartha
Palechor-Ceron, Nancy
Brandt, Sabine
Luff, Jennifer
Liu, Xuefeng
Schlegel, Richard
Yuan, Hang
author_sort Alkhilaiwi, Faris
collection PubMed
description BACKGROUND: Skin injuries in horses frequently lead to chronic wounds that lack a keratinocyte cover essential for healing. The limited proliferation of equine keratinocytes using current protocols has limited their use for regenerative medicine. Previously, equine induced pluripotent stem cells (eiPSCs) have been produced, and eiPSCs could be differentiated into equine keratinocytes suitable for stem cell-based skin constructs. However, the procedure is technically challenging and time-consuming. The present study was designed to evaluate whether conditional reprogramming (CR) could expand primary equine keratinocytes rapidly in an undifferentiated state but retain their ability to differentiate normally and form stratified epithelium. METHODS: Conditional reprogramming was used to isolate and propagate two equine keratinocyte cultures. PCR and FISH were employed to evaluate the equine origin of the cells and karyotyping to perform a chromosomal count. FACS analysis and immunofluorescence were used to determine the purity of equine keratinocytes and their proliferative state. Three-dimensional air-liquid interphase method was used to test the ability of cells to differentiate and form stratified squamous epithelium. RESULTS: Conditional reprogramming was an efficient method to isolate and propagate two equine keratinocyte cultures. Cells were propagated at the rate of 2.39 days/doubling for more than 40 population doublings. A feeder-free culture method was also developed for long-term expansion. Rock-inhibitor is critical for both feeder and feeder-free conditions and for maintaining the proliferating cells in a stem-like state. PCR and FISH validated equine-specific markers in the cultures. Karyotyping showed normal equine 64, XY chromosomes. FACS using pan-cytokeratin antibodies showed a pure population of keratinocytes. When ROCK inhibitor was withdrawn and the cells were transferred to a three-dimensional air-liquid culture, they formed a well-differentiated stratified squamous epithelium, which was positive for terminal differentiation markers. CONCLUSIONS: Our results prove that conditional reprogramming is the first method that allows for the rapid and continued in vitro propagation of primary equine keratinocytes. These unlimited supplies of autologous cells could be used to generate transplants without the risk of immune rejection. This offers the opportunity for treating recalcitrant horse wounds using autologous transplantation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0918-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6032561
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-60325612018-07-11 Long-term expansion of primary equine keratinocytes that maintain the ability to differentiate into stratified epidermis Alkhilaiwi, Faris Wang, Liqing Zhou, Dan Raudsepp, Terje Ghosh, Sharmila Paul, Siddartha Palechor-Ceron, Nancy Brandt, Sabine Luff, Jennifer Liu, Xuefeng Schlegel, Richard Yuan, Hang Stem Cell Res Ther Research BACKGROUND: Skin injuries in horses frequently lead to chronic wounds that lack a keratinocyte cover essential for healing. The limited proliferation of equine keratinocytes using current protocols has limited their use for regenerative medicine. Previously, equine induced pluripotent stem cells (eiPSCs) have been produced, and eiPSCs could be differentiated into equine keratinocytes suitable for stem cell-based skin constructs. However, the procedure is technically challenging and time-consuming. The present study was designed to evaluate whether conditional reprogramming (CR) could expand primary equine keratinocytes rapidly in an undifferentiated state but retain their ability to differentiate normally and form stratified epithelium. METHODS: Conditional reprogramming was used to isolate and propagate two equine keratinocyte cultures. PCR and FISH were employed to evaluate the equine origin of the cells and karyotyping to perform a chromosomal count. FACS analysis and immunofluorescence were used to determine the purity of equine keratinocytes and their proliferative state. Three-dimensional air-liquid interphase method was used to test the ability of cells to differentiate and form stratified squamous epithelium. RESULTS: Conditional reprogramming was an efficient method to isolate and propagate two equine keratinocyte cultures. Cells were propagated at the rate of 2.39 days/doubling for more than 40 population doublings. A feeder-free culture method was also developed for long-term expansion. Rock-inhibitor is critical for both feeder and feeder-free conditions and for maintaining the proliferating cells in a stem-like state. PCR and FISH validated equine-specific markers in the cultures. Karyotyping showed normal equine 64, XY chromosomes. FACS using pan-cytokeratin antibodies showed a pure population of keratinocytes. When ROCK inhibitor was withdrawn and the cells were transferred to a three-dimensional air-liquid culture, they formed a well-differentiated stratified squamous epithelium, which was positive for terminal differentiation markers. CONCLUSIONS: Our results prove that conditional reprogramming is the first method that allows for the rapid and continued in vitro propagation of primary equine keratinocytes. These unlimited supplies of autologous cells could be used to generate transplants without the risk of immune rejection. This offers the opportunity for treating recalcitrant horse wounds using autologous transplantation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0918-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-04 /pmc/articles/PMC6032561/ /pubmed/29973296 http://dx.doi.org/10.1186/s13287-018-0918-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Alkhilaiwi, Faris
Wang, Liqing
Zhou, Dan
Raudsepp, Terje
Ghosh, Sharmila
Paul, Siddartha
Palechor-Ceron, Nancy
Brandt, Sabine
Luff, Jennifer
Liu, Xuefeng
Schlegel, Richard
Yuan, Hang
Long-term expansion of primary equine keratinocytes that maintain the ability to differentiate into stratified epidermis
title Long-term expansion of primary equine keratinocytes that maintain the ability to differentiate into stratified epidermis
title_full Long-term expansion of primary equine keratinocytes that maintain the ability to differentiate into stratified epidermis
title_fullStr Long-term expansion of primary equine keratinocytes that maintain the ability to differentiate into stratified epidermis
title_full_unstemmed Long-term expansion of primary equine keratinocytes that maintain the ability to differentiate into stratified epidermis
title_short Long-term expansion of primary equine keratinocytes that maintain the ability to differentiate into stratified epidermis
title_sort long-term expansion of primary equine keratinocytes that maintain the ability to differentiate into stratified epidermis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032561/
https://www.ncbi.nlm.nih.gov/pubmed/29973296
http://dx.doi.org/10.1186/s13287-018-0918-x
work_keys_str_mv AT alkhilaiwifaris longtermexpansionofprimaryequinekeratinocytesthatmaintaintheabilitytodifferentiateintostratifiedepidermis
AT wangliqing longtermexpansionofprimaryequinekeratinocytesthatmaintaintheabilitytodifferentiateintostratifiedepidermis
AT zhoudan longtermexpansionofprimaryequinekeratinocytesthatmaintaintheabilitytodifferentiateintostratifiedepidermis
AT raudseppterje longtermexpansionofprimaryequinekeratinocytesthatmaintaintheabilitytodifferentiateintostratifiedepidermis
AT ghoshsharmila longtermexpansionofprimaryequinekeratinocytesthatmaintaintheabilitytodifferentiateintostratifiedepidermis
AT paulsiddartha longtermexpansionofprimaryequinekeratinocytesthatmaintaintheabilitytodifferentiateintostratifiedepidermis
AT palechorceronnancy longtermexpansionofprimaryequinekeratinocytesthatmaintaintheabilitytodifferentiateintostratifiedepidermis
AT brandtsabine longtermexpansionofprimaryequinekeratinocytesthatmaintaintheabilitytodifferentiateintostratifiedepidermis
AT luffjennifer longtermexpansionofprimaryequinekeratinocytesthatmaintaintheabilitytodifferentiateintostratifiedepidermis
AT liuxuefeng longtermexpansionofprimaryequinekeratinocytesthatmaintaintheabilitytodifferentiateintostratifiedepidermis
AT schlegelrichard longtermexpansionofprimaryequinekeratinocytesthatmaintaintheabilitytodifferentiateintostratifiedepidermis
AT yuanhang longtermexpansionofprimaryequinekeratinocytesthatmaintaintheabilitytodifferentiateintostratifiedepidermis