The Potentials and Pitfalls of a Human Cervical Organoid Model Including Langerhans Cells

Three-dimensional cell culturing to capture a life-like experimental environment has become a versatile tool for basic and clinical research. Mucosal and skin tissues can be grown as “organoids” in a petri dish and serve a wide variety of research questions. Here, we report our experience with human...

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Main Authors: Robert Jackson, Jordan D. Lukacs, Ingeborg Zehbe
Format: Article
Language:English
Published: MDPI AG 2020-12-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/12/12/1375
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spelling doaj-e9ade32b66424784904810c9329e15de2020-12-02T00:02:21ZengMDPI AGViruses1999-49152020-12-01121375137510.3390/v12121375The Potentials and Pitfalls of a Human Cervical Organoid Model Including Langerhans CellsRobert Jackson0Jordan D. Lukacs1Ingeborg Zehbe2Biotechnology Program, Lakehead University, Thunder Bay, ON P7B 5E1, CanadaDepartment of Biology, Lakehead University, Thunder Bay, ON P7B 5E1, CanadaProbe Development and Biomarker Exploration, Thunder Bay Regional Health Research Institute, Thunder Bay, ON P7B 6V4, CanadaThree-dimensional cell culturing to capture a life-like experimental environment has become a versatile tool for basic and clinical research. Mucosal and skin tissues can be grown as “organoids” in a petri dish and serve a wide variety of research questions. Here, we report our experience with human cervical organoids which could also include an immune component, e.g., Langerhans cells. We employ commercially available human cervical keratinocytes and fibroblasts as well as a myeloid cell line matured and purified into langerin-positive Langerhans cells. These are then seeded on a layer of keratinocytes with underlying dermal equivalent. Using about 10-fold more than the reported number in healthy cervical tissue (1–3%), we obtain differentiated cervical epithelium after 14 days with ~1% being Langerhans cells. We provide a detailed protocol for interested researchers to apply the described “aseptic” organoid model for all sorts of investigations—with or without Langerhans cells.https://www.mdpi.com/1999-4915/12/12/1375cervicalkeratinocytesorganoidsMUTZ cell lineLangerhans cells
collection DOAJ
language English
format Article
sources DOAJ
author Robert Jackson
Jordan D. Lukacs
Ingeborg Zehbe
spellingShingle Robert Jackson
Jordan D. Lukacs
Ingeborg Zehbe
The Potentials and Pitfalls of a Human Cervical Organoid Model Including Langerhans Cells
Viruses
cervical
keratinocytes
organoids
MUTZ cell line
Langerhans cells
author_facet Robert Jackson
Jordan D. Lukacs
Ingeborg Zehbe
author_sort Robert Jackson
title The Potentials and Pitfalls of a Human Cervical Organoid Model Including Langerhans Cells
title_short The Potentials and Pitfalls of a Human Cervical Organoid Model Including Langerhans Cells
title_full The Potentials and Pitfalls of a Human Cervical Organoid Model Including Langerhans Cells
title_fullStr The Potentials and Pitfalls of a Human Cervical Organoid Model Including Langerhans Cells
title_full_unstemmed The Potentials and Pitfalls of a Human Cervical Organoid Model Including Langerhans Cells
title_sort potentials and pitfalls of a human cervical organoid model including langerhans cells
publisher MDPI AG
series Viruses
issn 1999-4915
publishDate 2020-12-01
description Three-dimensional cell culturing to capture a life-like experimental environment has become a versatile tool for basic and clinical research. Mucosal and skin tissues can be grown as “organoids” in a petri dish and serve a wide variety of research questions. Here, we report our experience with human cervical organoids which could also include an immune component, e.g., Langerhans cells. We employ commercially available human cervical keratinocytes and fibroblasts as well as a myeloid cell line matured and purified into langerin-positive Langerhans cells. These are then seeded on a layer of keratinocytes with underlying dermal equivalent. Using about 10-fold more than the reported number in healthy cervical tissue (1–3%), we obtain differentiated cervical epithelium after 14 days with ~1% being Langerhans cells. We provide a detailed protocol for interested researchers to apply the described “aseptic” organoid model for all sorts of investigations—with or without Langerhans cells.
topic cervical
keratinocytes
organoids
MUTZ cell line
Langerhans cells
url https://www.mdpi.com/1999-4915/12/12/1375
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