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The effects of selected Australian snake venoms on tumour-associated microvascular endothelial cells (TAMECs) in vitro

The effects of various viperid and elapid venoms on the cellular biology of tumour-associated microvascular endothelial cells (TAMECs) were determined in the current study using cells isolated from a rat mammary adenocarcinoma. Previous studies to determine the effects of snake venoms on endothelial...

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Autores principales: Bateman, Emma, Venning, Michael, Mirtschin, Peter, Woods, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Library Publishing Media 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812074/
https://www.ncbi.nlm.nih.gov/pubmed/24191190
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author Bateman, Emma
Venning, Michael
Mirtschin, Peter
Woods, Anthony
author_facet Bateman, Emma
Venning, Michael
Mirtschin, Peter
Woods, Anthony
author_sort Bateman, Emma
collection PubMed
description The effects of various viperid and elapid venoms on the cellular biology of tumour-associated microvascular endothelial cells (TAMECs) were determined in the current study using cells isolated from a rat mammary adenocarcinoma. Previous studies to determine the effects of snake venoms on endothelial cells in vitro have in the main been performed on either human umbilical vein endothelial cells (HUVECs), bovine aortic endothelial cells (BAECs) or endothelial cell lines. These cell populations are accessible and easy to maintain in culture, however, it is well established that endothelial cells display vast heterogeneity depending upon the local microenvironment of the tissue from which they are isolated. Vascular targeting agents have been isolated from a variety of snake venoms, particularly from snakes of the Viperidae family, but it is yet to be established to what extent the venoms from Australian elapids possess similar vascular targeting properties. The present study used endothelial cells (ECs) isolated from the microvasculature of a rat mammary adenocarcinoma to determine the effects of a panel of snake venoms, including viperid venoms with known apoptotic activity and elapid venoms (both exotic and indigenous to Australia), on endothelial morphology and viability, paying specific attention to apoptotic responses. Three of the five Australian snake venoms investigated in this study elicited significant apoptotic responses in ECs which were in many ways similar to responses elicited by the selected viperid venoms. This suggests that these Australian elapids may possess vascular targeting components similar to those found within viperid venoms.
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spelling pubmed-38120742013-11-04 The effects of selected Australian snake venoms on tumour-associated microvascular endothelial cells (TAMECs) in vitro Bateman, Emma Venning, Michael Mirtschin, Peter Woods, Anthony J Venom Res Research Article The effects of various viperid and elapid venoms on the cellular biology of tumour-associated microvascular endothelial cells (TAMECs) were determined in the current study using cells isolated from a rat mammary adenocarcinoma. Previous studies to determine the effects of snake venoms on endothelial cells in vitro have in the main been performed on either human umbilical vein endothelial cells (HUVECs), bovine aortic endothelial cells (BAECs) or endothelial cell lines. These cell populations are accessible and easy to maintain in culture, however, it is well established that endothelial cells display vast heterogeneity depending upon the local microenvironment of the tissue from which they are isolated. Vascular targeting agents have been isolated from a variety of snake venoms, particularly from snakes of the Viperidae family, but it is yet to be established to what extent the venoms from Australian elapids possess similar vascular targeting properties. The present study used endothelial cells (ECs) isolated from the microvasculature of a rat mammary adenocarcinoma to determine the effects of a panel of snake venoms, including viperid venoms with known apoptotic activity and elapid venoms (both exotic and indigenous to Australia), on endothelial morphology and viability, paying specific attention to apoptotic responses. Three of the five Australian snake venoms investigated in this study elicited significant apoptotic responses in ECs which were in many ways similar to responses elicited by the selected viperid venoms. This suggests that these Australian elapids may possess vascular targeting components similar to those found within viperid venoms. Library Publishing Media 2013-10-19 /pmc/articles/PMC3812074/ /pubmed/24191190 Text en © Copyright The Author(s) http://creativecommons.org/licenses/by-nc/2.5 Published by Library Publishing Media. This is an open access article, published under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5). This license permits non-commercial use, distribution and reproduction of the article, provided the original work is appropriately acknowledged with correct citation details.
spellingShingle Research Article
Bateman, Emma
Venning, Michael
Mirtschin, Peter
Woods, Anthony
The effects of selected Australian snake venoms on tumour-associated microvascular endothelial cells (TAMECs) in vitro
title The effects of selected Australian snake venoms on tumour-associated microvascular endothelial cells (TAMECs) in vitro
title_full The effects of selected Australian snake venoms on tumour-associated microvascular endothelial cells (TAMECs) in vitro
title_fullStr The effects of selected Australian snake venoms on tumour-associated microvascular endothelial cells (TAMECs) in vitro
title_full_unstemmed The effects of selected Australian snake venoms on tumour-associated microvascular endothelial cells (TAMECs) in vitro
title_short The effects of selected Australian snake venoms on tumour-associated microvascular endothelial cells (TAMECs) in vitro
title_sort effects of selected australian snake venoms on tumour-associated microvascular endothelial cells (tamecs) in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812074/
https://www.ncbi.nlm.nih.gov/pubmed/24191190
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