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Regulation of endothelial Fas expression as a mechanism of promotion of vascular integrity by mural cells in tumors

Angiogenesis is a multi‐step process that culminates in vascular maturation whereby nascent vessels stabilize to become functional, and mural cells play an essential role in this process. Recent studies have shown that mural cells in tumors also promote and maintain vascular integrity, with wide‐rea...

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Autores principales: Kamei, Ryosuke, Tanaka, Hiroyoshi Y., Kawano, Takao, Morii, Chiharu, Tanaka, Sayaka, Nishihara, Hiroshi, Iwata, Caname, Kano, Mitsunobu R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448593/
https://www.ncbi.nlm.nih.gov/pubmed/28247971
http://dx.doi.org/10.1111/cas.13216
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author Kamei, Ryosuke
Tanaka, Hiroyoshi Y.
Kawano, Takao
Morii, Chiharu
Tanaka, Sayaka
Nishihara, Hiroshi
Iwata, Caname
Kano, Mitsunobu R.
author_facet Kamei, Ryosuke
Tanaka, Hiroyoshi Y.
Kawano, Takao
Morii, Chiharu
Tanaka, Sayaka
Nishihara, Hiroshi
Iwata, Caname
Kano, Mitsunobu R.
author_sort Kamei, Ryosuke
collection PubMed
description Angiogenesis is a multi‐step process that culminates in vascular maturation whereby nascent vessels stabilize to become functional, and mural cells play an essential role in this process. Recent studies have shown that mural cells in tumors also promote and maintain vascular integrity, with wide‐reaching clinical implications including the regulation of tumor growth, metastases, and drug delivery. Various regulatory signaling pathways have been hitherto implicated, but whether regulation of Fas‐dependent apoptotic mechanisms is involved has not yet been fully investigated. We first compared endothelial FAS staining in human pancreatic ductal adenocarcinomas and colon carcinomas and show that the latter, characterized by lower mural cell coverage of tumor vasculature, demonstrated higher expression of FAS than the former. Next, in an in vitro coculture system of MS‐1 and 10T1/2 cells as endothelial and mural cells respectively, we show that mural cells decreased endothelial Fas expression. Then, in an in vivo model in which C26 colon carcinoma cells were inoculated together with MS‐1 cells alone or with the further addition of 10T1/2 cells, we demonstrate that mural cells prevented hemorrhage. Finally, knockdown of endothelial Fas sufficiently recapitulated the protection against hemorrhage seen with the addition of mural cells. These results together suggest that regulation of endothelial Fas signaling is involved in the promotion of vascular integrity by mural cells in tumors.
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spelling pubmed-54485932017-06-01 Regulation of endothelial Fas expression as a mechanism of promotion of vascular integrity by mural cells in tumors Kamei, Ryosuke Tanaka, Hiroyoshi Y. Kawano, Takao Morii, Chiharu Tanaka, Sayaka Nishihara, Hiroshi Iwata, Caname Kano, Mitsunobu R. Cancer Sci Original Articles Angiogenesis is a multi‐step process that culminates in vascular maturation whereby nascent vessels stabilize to become functional, and mural cells play an essential role in this process. Recent studies have shown that mural cells in tumors also promote and maintain vascular integrity, with wide‐reaching clinical implications including the regulation of tumor growth, metastases, and drug delivery. Various regulatory signaling pathways have been hitherto implicated, but whether regulation of Fas‐dependent apoptotic mechanisms is involved has not yet been fully investigated. We first compared endothelial FAS staining in human pancreatic ductal adenocarcinomas and colon carcinomas and show that the latter, characterized by lower mural cell coverage of tumor vasculature, demonstrated higher expression of FAS than the former. Next, in an in vitro coculture system of MS‐1 and 10T1/2 cells as endothelial and mural cells respectively, we show that mural cells decreased endothelial Fas expression. Then, in an in vivo model in which C26 colon carcinoma cells were inoculated together with MS‐1 cells alone or with the further addition of 10T1/2 cells, we demonstrate that mural cells prevented hemorrhage. Finally, knockdown of endothelial Fas sufficiently recapitulated the protection against hemorrhage seen with the addition of mural cells. These results together suggest that regulation of endothelial Fas signaling is involved in the promotion of vascular integrity by mural cells in tumors. John Wiley and Sons Inc. 2017-05-24 2017-05 /pmc/articles/PMC5448593/ /pubmed/28247971 http://dx.doi.org/10.1111/cas.13216 Text en © 2017 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Kamei, Ryosuke
Tanaka, Hiroyoshi Y.
Kawano, Takao
Morii, Chiharu
Tanaka, Sayaka
Nishihara, Hiroshi
Iwata, Caname
Kano, Mitsunobu R.
Regulation of endothelial Fas expression as a mechanism of promotion of vascular integrity by mural cells in tumors
title Regulation of endothelial Fas expression as a mechanism of promotion of vascular integrity by mural cells in tumors
title_full Regulation of endothelial Fas expression as a mechanism of promotion of vascular integrity by mural cells in tumors
title_fullStr Regulation of endothelial Fas expression as a mechanism of promotion of vascular integrity by mural cells in tumors
title_full_unstemmed Regulation of endothelial Fas expression as a mechanism of promotion of vascular integrity by mural cells in tumors
title_short Regulation of endothelial Fas expression as a mechanism of promotion of vascular integrity by mural cells in tumors
title_sort regulation of endothelial fas expression as a mechanism of promotion of vascular integrity by mural cells in tumors
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448593/
https://www.ncbi.nlm.nih.gov/pubmed/28247971
http://dx.doi.org/10.1111/cas.13216
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