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Specific tumor-stroma interactions of EBV-positive Burkitt's lymphoma cells in the chick chorioallantoic membrane

BACKGROUND: Burkitt's lymphoma (BL) is an aggressive Non-Hodgkin lymphoma. Epstein-Barr Virus (EBV) is able to transform B cells and is a causative infectious agent in BL. The precise role of EBV in lymphoma progression is still unclear. Most investigations have concentrated on cell autonomous...

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Autores principales: Becker, Jürgen, Covelo-Fernandez, Ana, von Bonin, Frederike, Kube, Dieter, Wilting, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325879/
https://www.ncbi.nlm.nih.gov/pubmed/22404859
http://dx.doi.org/10.1186/2045-824X-4-3
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author Becker, Jürgen
Covelo-Fernandez, Ana
von Bonin, Frederike
Kube, Dieter
Wilting, Jörg
author_facet Becker, Jürgen
Covelo-Fernandez, Ana
von Bonin, Frederike
Kube, Dieter
Wilting, Jörg
author_sort Becker, Jürgen
collection PubMed
description BACKGROUND: Burkitt's lymphoma (BL) is an aggressive Non-Hodgkin lymphoma. Epstein-Barr Virus (EBV) is able to transform B cells and is a causative infectious agent in BL. The precise role of EBV in lymphoma progression is still unclear. Most investigations have concentrated on cell autonomous functions of EBV in B cells. Functions of the local environment in BL progression have rarely been studied, mainly due to the lack of appropriate in vivo models. Therefore, we inoculated different human BL cell-lines onto the chorioallantoic membrane (CAM) of embryonic day 10 (ED10) chick embryos and re-incubated until ED14 and ED17. RESULTS: All cell-lines formed solid tumors. However, we observed strong differences in the behavior of EBV(+ )and EBV(- )cell-lines. Tumor borders of EBV(+ )cells were very fuzzy and numerous cells migrated into the CAM. In EBV(- )tumors, the borders were much better defined. In contrast to EBV(- )cells, the EBV(+ )cells induced massive immigration of chick leukocytes at the tumor borders and the development of granulation tissue with large numbers of blood vessels and lymphatics, although the expression of pro- and anti-angiogenic forms of Vascular Endothelial Growth Factors/receptors was the same in all BL cell-lines tested. The EBV(+ )cell-lines massively disseminated via the lymphatics and completely occluded them. CONCLUSIONS: Our data suggest that the EBV(+ )cells attract pro-angiogenic leukocytes, which then induce secondary tumor-stroma interactions contributing to the progression of BL. We show that the CAM is a highly suitable in vivo model to study the differential behavior of BL cell-lines.
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spelling pubmed-33258792012-04-14 Specific tumor-stroma interactions of EBV-positive Burkitt's lymphoma cells in the chick chorioallantoic membrane Becker, Jürgen Covelo-Fernandez, Ana von Bonin, Frederike Kube, Dieter Wilting, Jörg Vasc Cell Research BACKGROUND: Burkitt's lymphoma (BL) is an aggressive Non-Hodgkin lymphoma. Epstein-Barr Virus (EBV) is able to transform B cells and is a causative infectious agent in BL. The precise role of EBV in lymphoma progression is still unclear. Most investigations have concentrated on cell autonomous functions of EBV in B cells. Functions of the local environment in BL progression have rarely been studied, mainly due to the lack of appropriate in vivo models. Therefore, we inoculated different human BL cell-lines onto the chorioallantoic membrane (CAM) of embryonic day 10 (ED10) chick embryos and re-incubated until ED14 and ED17. RESULTS: All cell-lines formed solid tumors. However, we observed strong differences in the behavior of EBV(+ )and EBV(- )cell-lines. Tumor borders of EBV(+ )cells were very fuzzy and numerous cells migrated into the CAM. In EBV(- )tumors, the borders were much better defined. In contrast to EBV(- )cells, the EBV(+ )cells induced massive immigration of chick leukocytes at the tumor borders and the development of granulation tissue with large numbers of blood vessels and lymphatics, although the expression of pro- and anti-angiogenic forms of Vascular Endothelial Growth Factors/receptors was the same in all BL cell-lines tested. The EBV(+ )cell-lines massively disseminated via the lymphatics and completely occluded them. CONCLUSIONS: Our data suggest that the EBV(+ )cells attract pro-angiogenic leukocytes, which then induce secondary tumor-stroma interactions contributing to the progression of BL. We show that the CAM is a highly suitable in vivo model to study the differential behavior of BL cell-lines. BioMed Central 2012-03-09 /pmc/articles/PMC3325879/ /pubmed/22404859 http://dx.doi.org/10.1186/2045-824X-4-3 Text en Copyright ©2012 Becker et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Becker, Jürgen
Covelo-Fernandez, Ana
von Bonin, Frederike
Kube, Dieter
Wilting, Jörg
Specific tumor-stroma interactions of EBV-positive Burkitt's lymphoma cells in the chick chorioallantoic membrane
title Specific tumor-stroma interactions of EBV-positive Burkitt's lymphoma cells in the chick chorioallantoic membrane
title_full Specific tumor-stroma interactions of EBV-positive Burkitt's lymphoma cells in the chick chorioallantoic membrane
title_fullStr Specific tumor-stroma interactions of EBV-positive Burkitt's lymphoma cells in the chick chorioallantoic membrane
title_full_unstemmed Specific tumor-stroma interactions of EBV-positive Burkitt's lymphoma cells in the chick chorioallantoic membrane
title_short Specific tumor-stroma interactions of EBV-positive Burkitt's lymphoma cells in the chick chorioallantoic membrane
title_sort specific tumor-stroma interactions of ebv-positive burkitt's lymphoma cells in the chick chorioallantoic membrane
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325879/
https://www.ncbi.nlm.nih.gov/pubmed/22404859
http://dx.doi.org/10.1186/2045-824X-4-3
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