Keratinocyte Culture: Siriraj's Experience

Objective: Cell-based therapy is gaining increasing prominence in medicine, where it has the potential to replace or repair damaged tissue using new engineered cells. Skin cell engineering, also known as keratinocyte culture or cultured epithelial autograft (CEA), is a promising field in cell-based...

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Main Authors: Chongdee Aojanepong, Kongsawate Khaogate, Adisak Wongkajornsilp, Sunisa Duangsa-ard, Kanda Kasetsinsombat
Other Authors: Siriraj Hospital
Format: Article
Published: 2022
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/74554
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spelling th-mahidol.745542022-08-04T11:22:54Z Keratinocyte Culture: Siriraj's Experience Chongdee Aojanepong Kongsawate Khaogate Adisak Wongkajornsilp Sunisa Duangsa-ard Kanda Kasetsinsombat Siriraj Hospital Division of Plastic Surgery Medicine Objective: Cell-based therapy is gaining increasing prominence in medicine, where it has the potential to replace or repair damaged tissue using new engineered cells. Skin cell engineering, also known as keratinocyte culture or cultured epithelial autograft (CEA), is a promising field in cell-based therapy. CEA is now used in many parts of the world as an alternative treatment for some diseases that require large defects to be covered, such as severe and major burn patients and congenital melanocytic nevus. The use of CEA in conjunction with acellular skin substitution is rapidly expanding. Materials and Methods: This study is an initiative aimed at supporting the production and use of keratinocyte cultures at Siriraj Hospital. This is the first stage of developing sheet keratinocyte culture in vitro. Results: Our study yielded very promising results. As feeder cells, we used irradiated 3T3 murine fibroblasts, as per the standard protocol for keratinocyte culture. The growth duration was four weeks: 2 weeks for the 3T3 murine fibroblasts and 2 weeks for the keratinocytes. The keratinocytes grew rapidly and formed sheets with irradiated 3T3 murine fibroblasts. The retrieval of the cell sheets was straightforward thanks to the temperature-response cell culture dish and halo-ring cell recovery sheet. Flow cytometry revealed that the cells had a very high viability and purity. H&E staining revealed the sheets comprised two to four layers of stratified epithelial tissue. Conclusion: From this study, our method of manufacturing the CEA can offer a promising result. This can be use in the treatment which require large skin coverage. However, we aim to initiate animal and human trial phase next. 2022-08-04T04:22:54Z 2022-08-04T04:22:54Z 2022-05-01 Article Siriraj Medical Journal. Vol.74, No.5 (2022), 274-283 10.33192/Smj.2022.34 22288082 2-s2.0-85129972925 https://repository.li.mahidol.ac.th/handle/123456789/74554 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85129972925&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
Chongdee Aojanepong
Kongsawate Khaogate
Adisak Wongkajornsilp
Sunisa Duangsa-ard
Kanda Kasetsinsombat
Keratinocyte Culture: Siriraj's Experience
description Objective: Cell-based therapy is gaining increasing prominence in medicine, where it has the potential to replace or repair damaged tissue using new engineered cells. Skin cell engineering, also known as keratinocyte culture or cultured epithelial autograft (CEA), is a promising field in cell-based therapy. CEA is now used in many parts of the world as an alternative treatment for some diseases that require large defects to be covered, such as severe and major burn patients and congenital melanocytic nevus. The use of CEA in conjunction with acellular skin substitution is rapidly expanding. Materials and Methods: This study is an initiative aimed at supporting the production and use of keratinocyte cultures at Siriraj Hospital. This is the first stage of developing sheet keratinocyte culture in vitro. Results: Our study yielded very promising results. As feeder cells, we used irradiated 3T3 murine fibroblasts, as per the standard protocol for keratinocyte culture. The growth duration was four weeks: 2 weeks for the 3T3 murine fibroblasts and 2 weeks for the keratinocytes. The keratinocytes grew rapidly and formed sheets with irradiated 3T3 murine fibroblasts. The retrieval of the cell sheets was straightforward thanks to the temperature-response cell culture dish and halo-ring cell recovery sheet. Flow cytometry revealed that the cells had a very high viability and purity. H&E staining revealed the sheets comprised two to four layers of stratified epithelial tissue. Conclusion: From this study, our method of manufacturing the CEA can offer a promising result. This can be use in the treatment which require large skin coverage. However, we aim to initiate animal and human trial phase next.
author2 Siriraj Hospital
author_facet Siriraj Hospital
Chongdee Aojanepong
Kongsawate Khaogate
Adisak Wongkajornsilp
Sunisa Duangsa-ard
Kanda Kasetsinsombat
format Article
author Chongdee Aojanepong
Kongsawate Khaogate
Adisak Wongkajornsilp
Sunisa Duangsa-ard
Kanda Kasetsinsombat
author_sort Chongdee Aojanepong
title Keratinocyte Culture: Siriraj's Experience
title_short Keratinocyte Culture: Siriraj's Experience
title_full Keratinocyte Culture: Siriraj's Experience
title_fullStr Keratinocyte Culture: Siriraj's Experience
title_full_unstemmed Keratinocyte Culture: Siriraj's Experience
title_sort keratinocyte culture: siriraj's experience
publishDate 2022
url https://repository.li.mahidol.ac.th/handle/123456789/74554
_version_ 1763491118383628288