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Investigation of brain tissue infiltration by medulloblastoma cells in an ex vivo model
Medulloblastoma (MB) is a paediatric cancer of the cerebellum that can develop cerebellar and leptomeningeal metastases. Local brain tissue infiltration, the underlying cause of metastasis and relapse, remains unexplored. We developed a novel approach to investigate tissue infiltration of MB using o...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509741/ https://www.ncbi.nlm.nih.gov/pubmed/28706234 http://dx.doi.org/10.1038/s41598-017-05573-w |
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author | Neve, Anuja Santhana Kumar, Karthiga Tripolitsioti, Dimitra Grotzer, Michael A. Baumgartner, Martin |
author_facet | Neve, Anuja Santhana Kumar, Karthiga Tripolitsioti, Dimitra Grotzer, Michael A. Baumgartner, Martin |
author_sort | Neve, Anuja |
collection | PubMed |
description | Medulloblastoma (MB) is a paediatric cancer of the cerebellum that can develop cerebellar and leptomeningeal metastases. Local brain tissue infiltration, the underlying cause of metastasis and relapse, remains unexplored. We developed a novel approach to investigate tissue infiltration of MB using organotypic cerebellum slice culture (OCSC). We show that cellular and structural components of cerebellar tissue in OCSCs are maintained for up to 30 days ex vivo, and that OCSCs foster tumour growth and cell proliferation. Using cell-based models of sonic hedgehog (SHH) and group 3 (G3) MB, we quantified tumour growth and infiltration and determined the morphological characteristics of the infiltrating cells. We observed basal levels of dissemination occurring in both subgroups with cells migrating either individually or collectively as clusters. Collective cerebellar tissue infiltration of SHH MB cells was further enhanced by EGF but not HGF, demonstrating differential tumour cell responses to microenvironmental cues. We found G3 cells to be hyper proliferative and observed aggressive tumour expansion even in the absence of exogenous growth factors. Our study thus provides unprecedented insights into brain tissue infiltration of SHH and G3 MB cells and reveals the cellular basis of the tumour progressing functions of EGF in SHH MB. |
format | Online Article Text |
id | pubmed-5509741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55097412017-07-17 Investigation of brain tissue infiltration by medulloblastoma cells in an ex vivo model Neve, Anuja Santhana Kumar, Karthiga Tripolitsioti, Dimitra Grotzer, Michael A. Baumgartner, Martin Sci Rep Article Medulloblastoma (MB) is a paediatric cancer of the cerebellum that can develop cerebellar and leptomeningeal metastases. Local brain tissue infiltration, the underlying cause of metastasis and relapse, remains unexplored. We developed a novel approach to investigate tissue infiltration of MB using organotypic cerebellum slice culture (OCSC). We show that cellular and structural components of cerebellar tissue in OCSCs are maintained for up to 30 days ex vivo, and that OCSCs foster tumour growth and cell proliferation. Using cell-based models of sonic hedgehog (SHH) and group 3 (G3) MB, we quantified tumour growth and infiltration and determined the morphological characteristics of the infiltrating cells. We observed basal levels of dissemination occurring in both subgroups with cells migrating either individually or collectively as clusters. Collective cerebellar tissue infiltration of SHH MB cells was further enhanced by EGF but not HGF, demonstrating differential tumour cell responses to microenvironmental cues. We found G3 cells to be hyper proliferative and observed aggressive tumour expansion even in the absence of exogenous growth factors. Our study thus provides unprecedented insights into brain tissue infiltration of SHH and G3 MB cells and reveals the cellular basis of the tumour progressing functions of EGF in SHH MB. Nature Publishing Group UK 2017-07-13 /pmc/articles/PMC5509741/ /pubmed/28706234 http://dx.doi.org/10.1038/s41598-017-05573-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Neve, Anuja Santhana Kumar, Karthiga Tripolitsioti, Dimitra Grotzer, Michael A. Baumgartner, Martin Investigation of brain tissue infiltration by medulloblastoma cells in an ex vivo model |
title | Investigation of brain tissue infiltration by medulloblastoma cells in an ex vivo model |
title_full | Investigation of brain tissue infiltration by medulloblastoma cells in an ex vivo model |
title_fullStr | Investigation of brain tissue infiltration by medulloblastoma cells in an ex vivo model |
title_full_unstemmed | Investigation of brain tissue infiltration by medulloblastoma cells in an ex vivo model |
title_short | Investigation of brain tissue infiltration by medulloblastoma cells in an ex vivo model |
title_sort | investigation of brain tissue infiltration by medulloblastoma cells in an ex vivo model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509741/ https://www.ncbi.nlm.nih.gov/pubmed/28706234 http://dx.doi.org/10.1038/s41598-017-05573-w |
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